Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1572 |
| ensemblid | ENSG00000197446.9 |
| hgncid | 2632 |
| symbol | CYP2F1 |
| name | cytochrome P450 family 2 subfamily F member 1 |
| refseq_nuc | NM_000774.5 |
| refseq_prot | NP_000765.2 |
| ensembl_nuc | ENST00000331105.7 |
| ensembl_prot | ENSP00000333534.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 41114432 |
| end | 41128381 |
| strand | + |
| ver | v1.2 |
| region | chr19:41114432-41128381 |
| region5000 | chr19:41109432-41133381 |
| regionname0 | CYP2F1_chr19_41114432_41128381 |
| regionname5000 | CYP2F1_chr19_41109432_41133381 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 491 | 167 | 17 | 31 | 94 | 9 | 14 | 69 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0002 | 0/0 | 26 | 114 | 45 | 13 | 36 | 4 | 16 | 25 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(21): Show |
chr19 | 41109432 | 41133381 |
| a0003 | 0/0 | 491 | 21 | 10 | 4 | 0 | 3 | 4 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0004 | 0/0 | 491 | 17 | 0 | 12 | 1 | 2 | 2 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0005 | 0/0 | 491 | 17 | 1 | 8 | 5 | 0 | 3 | 5 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0006 | 0/0 | 491 | 9 | 0 | 0 | 9 | 0 | 0 | 7 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0007 | 0/0 | 491 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0008 | 0/0 | 491 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0009 | 0/0 | 491 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0010 | 0/0 | 491 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0011 | 0/0 | 491 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0012 | 0/0 | 491 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0013 | 0/0 | 491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0014 | 0/0 | 491 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| a0015 | 0/0 | 491 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | MDSIS others(486): Show |
chr19 | 41109432 | 41133381 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1473 | 163 | 16 | 30 | 92 | 9 | 14 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0001c0015 | 0/0 | 1473 | 3 | 0 | 1 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0001c0027 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0002 | 0/0 | 1474 | 50 | 5 | 10 | 24 | 4 | 7 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0003 | 0/0 | 1474 | 26 | 18 | 3 | 5 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0005 | 0/0 | 1474 | 20 | 17 | 0 | 0 | 0 | 3 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0010 | 0/0 | 1474 | 5 | 0 | 0 | 1 | 0 | 4 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0017 | 0/0 | 1474 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0018 | 0/0 | 1474 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0019 | 0/0 | 1474 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0028 | 0/0 | 1474 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0029 | 0/0 | 1474 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0030 | 0/0 | 1474 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0031 | 0/0 | 1474 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0032 | 0/0 | 1474 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0033 | 0/0 | 1474 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0002c0034 | 0/0 | 1474 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1469): Show |
chr19 | 41109432 | 41133381 | ||
| a0003c0004 | 0/0 | 1473 | 21 | 10 | 4 | 0 | 3 | 4 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0004c0006 | 0/0 | 1473 | 17 | 0 | 12 | 1 | 2 | 2 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0005c0007 | 0/0 | 1473 | 16 | 0 | 8 | 5 | 0 | 3 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0005c0021 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0006c0008 | 0/0 | 1473 | 9 | 0 | 0 | 9 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0007c0009 | 0/0 | 1473 | 7 | 7 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0007c0016 | 0/0 | 1473 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0008c0012 | 0/0 | 1473 | 4 | 4 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0009c0011 | 0/0 | 1473 | 4 | 4 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0010c0023 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0010c0024 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0010c0026 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0011c0013 | 0/0 | 1473 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0012c0014 | 0/0 | 1473 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0013c0020 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0014c0025 | 0/0 | 1473 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 | ||
| a0015c0022 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | ATGGA others(1468): Show |
chr19 | 41109432 | 41133381 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1847 | 147 | 13 | 30 | 79 | 9 | 14 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0001c0001t0002 | 0/0 | 1848 | 4 | 2 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0001c0001t0004 | 0/0 | 1848 | 4 | 1 | 0 | 3 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0001c0001t0008 | 0/0 | 1847 | 7 | 0 | 0 | 7 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0001c0001t0015 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0001c0015t0001 | 0/0 | 1847 | 3 | 0 | 1 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0001c0027t0001 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0002c0002t0001 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0002c0002t0002 | 0/0 | 1849 | 47 | 4 | 10 | 22 | 4 | 7 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0002t0011 | 0/0 | 1849 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0002t0017 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0002c0003t0003 | 0/0 | 1848 | 26 | 18 | 3 | 5 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0002c0005t0002 | 0/0 | 1849 | 8 | 6 | 0 | 0 | 0 | 2 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0005t0006 | 0/0 | 1849 | 8 | 8 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0005t0010 | 0/0 | 1849 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0005t0014 | 0/0 | 1848 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0002c0010t0003 | 0/0 | 1848 | 5 | 0 | 0 | 1 | 0 | 4 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0002c0017t0002 | 0/0 | 1849 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0018t0003 | 0/0 | 1848 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0002c0019t0002 | 0/0 | 1849 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0028t0003 | 0/0 | 1848 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0002c0029t0003 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0002c0030t0002 | 0/0 | 1849 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0031t0002 | 0/0 | 1849 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0032t0002 | 0/0 | 1849 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0033t0002 | 0/0 | 1849 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0002c0034t0002 | 0/0 | 1849 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1844): Show |
chr19 | 41109432 | 41133381 |
| a0003c0004t0004 | 0/0 | 1848 | 21 | 10 | 4 | 0 | 3 | 4 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0004c0006t0002 | 0/0 | 1848 | 15 | 0 | 11 | 1 | 2 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0004c0006t0012 | 0/0 | 1847 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0004c0006t0013 | 0/0 | 1847 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0005c0007t0005 | 0/0 | 1848 | 16 | 0 | 8 | 5 | 0 | 3 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0005c0021t0002 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0006c0008t0007 | 0/0 | 1834 | 9 | 0 | 0 | 9 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1829): Show |
chr19 | 41109432 | 41133381 |
| a0007c0009t0001 | 0/0 | 1847 | 6 | 6 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0007c0009t0016 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0007c0016t0002 | 0/0 | 1848 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0008c0012t0009 | 0/0 | 1847 | 4 | 4 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0009c0011t0006 | 0/0 | 1848 | 4 | 4 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0010c0023t0009 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0010c0024t0002 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0010c0026t0002 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0011c0013t0002 | 0/0 | 1848 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0012c0014t0001 | 0/0 | 1847 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0013c0020t0002 | 0/0 | 1848 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1843): Show |
chr19 | 41109432 | 41133381 |
| a0014c0025t0001 | 0/0 | 1847 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| a0015c0022t0009 | 0/0 | 1847 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | AAGCA others(1842): Show |
chr19 | 41109432 | 41133381 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 2 | 6 | 2 | 3 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0002 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0004 | 1/0 | 8 | 0 | 5 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0005 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0015 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0052 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0008g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0001t0015g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0015t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0015t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0015t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0001c0027t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0003 | 0/0 | 8 | 1 | 3 | 2 | 1 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0007 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0033 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0011g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0002t0017g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0006g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0010g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0010g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0005t0014g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0010t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0010t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0010t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0010t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0010t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0017t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0017t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0018t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0018t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0019t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0019t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0028t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0029t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0030t0002g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0031t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0032t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0033t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0002c0034t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0003c0004t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0006 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0012g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0004c0006t0013g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0007t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0005c0021t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0006c0008t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0006c0008t0007g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0006c0008t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0006c0008t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0006c0008t0007g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0006c0008t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0006c0008t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0006c0008t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0007c0009t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0007c0009t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0007c0009t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0007c0009t0016g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0007c0016t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0007c0016t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0008c0012t0009g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0008c0012t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0008c0012t0009g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0009c0011t0006g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0009c0011t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0009c0011t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0010c0023t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0010c0024t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0010c0026t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0011c0013t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0011c0013t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0011c0013t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0012c0014t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0012c0014t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0012c0014t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0013c0020t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0014c0025t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| a0015c0022t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0081 | EUR | GBR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0032 | EUR | GBR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | GBR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0003 | EUR | FIN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00323 | hp1 | a0004 | c0006 | t0002 | g0075 | EUR | FIN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00323 | hp2 | a0004 | c0006 | t0002 | g0006 | EUR | FIN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0008 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00558 | hp1 | a0002 | c0002 | t0011 | g0020 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00558 | hp2 | a0002 | c0003 | t0003 | g0158 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0085 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00642 | hp1 | a0005 | c0007 | t0005 | g0108 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00642 | hp2 | a0002 | c0003 | t0003 | g0141 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0032 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00735 | hp2 | a0001 | c0015 | t0001 | g0011 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00738 | hp1 | a0002 | c0003 | t0003 | g0143 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0083 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG00741 | hp2 | a0003 | c0004 | t0004 | g0045 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01069 | hp1 | a0004 | c0006 | t0002 | g0072 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0092 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01106 | hp2 | a0003 | c0004 | t0004 | g0182 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01109 | hp2 | a0003 | c0004 | t0004 | g0183 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01167 | hp2 | a0005 | c0007 | t0005 | g0125 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01169 | hp2 | a0005 | c0007 | t0005 | g0111 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01175 | hp1 | a0004 | c0006 | t0002 | g0077 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01346 | hp1 | a0005 | c0007 | t0005 | g0013 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01358 | hp1 | a0004 | c0006 | t0002 | g0076 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01361 | hp2 | a0004 | c0006 | t0002 | g0006 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01516 | hp1 | a0003 | c0004 | t0004 | g0181 | EUR | IBS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01516 | hp2 | a0003 | c0004 | t0004 | g0046 | EUR | IBS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01517 | hp2 | a0003 | c0004 | t0004 | g0046 | EUR | IBS | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01884 | hp1 | a0002 | c0005 | t0006 | g0040 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01884 | hp2 | a0008 | c0012 | t0009 | g0161 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01891 | hp2 | a0002 | c0002 | t0017 | g0121 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0035 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0090 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01952 | hp2 | a0004 | c0006 | t0002 | g0006 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01975 | hp1 | a0005 | c0007 | t0005 | g0122 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01975 | hp2 | a0005 | c0007 | t0005 | g0124 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01978 | hp1 | a0004 | c0006 | t0002 | g0079 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01978 | hp2 | a0003 | c0004 | t0004 | g0170 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01981 | hp1 | a0004 | c0006 | t0002 | g0018 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01993 | hp1 | a0004 | c0006 | t0002 | g0073 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01993 | hp2 | a0005 | c0007 | t0005 | g0110 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02056 | hp2 | a0001 | c0001 | t0008 | g0009 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02080 | hp2 | a0006 | c0008 | t0007 | g0015 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0008 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02132 | hp2 | a0006 | c0008 | t0007 | g0187 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | KHV | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02145 | hp1 | a0002 | c0018 | t0003 | g0116 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02145 | hp2 | a0002 | c0003 | t0003 | g0021 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02155 | hp1 | a0001 | c0015 | t0001 | g0222 | EAS | CDX | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | CDX | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02165 | hp1 | a0001 | c0015 | t0001 | g0220 | EAS | CDX | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02165 | hp2 | a0001 | c0001 | t0008 | g0008 | EAS | CDX | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02257 | hp1 | a0002 | c0003 | t0003 | g0113 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02257 | hp2 | a0003 | c0004 | t0004 | g0014 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02258 | hp1 | a0002 | c0005 | t0002 | g0058 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02258 | hp2 | a0002 | c0018 | t0003 | g0115 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02280 | hp1 | a0003 | c0004 | t0004 | g0014 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02280 | hp2 | a0003 | c0004 | t0004 | g0014 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02293 | hp1 | a0004 | c0006 | t0013 | g0074 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02293 | hp2 | a0004 | c0006 | t0002 | g0006 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02300 | hp1 | a0004 | c0006 | t0002 | g0006 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02300 | hp2 | a0005 | c0007 | t0005 | g0112 | AMR | PEL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02451 | hp2 | a0002 | c0005 | t0002 | g0065 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02572 | hp1 | a0003 | c0004 | t0004 | g0179 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02572 | hp2 | a0010 | c0023 | t0009 | g0157 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02602 | hp2 | a0003 | c0004 | t0004 | g0212 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0131 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02615 | hp2 | a0007 | c0016 | t0002 | g0154 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02622 | hp1 | a0002 | c0003 | t0003 | g0037 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02630 | hp1 | a0007 | c0009 | t0001 | g0005 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02630 | hp2 | a0002 | c0005 | t0006 | g0120 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02647 | hp1 | a0002 | c0005 | t0006 | g0119 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02683 | hp1 | a0004 | c0006 | t0012 | g0078 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02683 | hp2 | a0002 | c0005 | t0014 | g0067 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02698 | hp1 | a0003 | c0004 | t0004 | g0171 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02717 | hp1 | a0007 | c0009 | t0016 | g0016 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02723 | hp2 | a0010 | c0024 | t0002 | g0127 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0095 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02738 | hp2 | a0014 | c0025 | t0001 | g0002 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02809 | hp2 | a0007 | c0009 | t0001 | g0193 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02818 | hp1 | a0003 | c0004 | t0004 | g0047 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02818 | hp2 | a0002 | c0003 | t0003 | g0144 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02886 | hp1 | a0008 | c0012 | t0009 | g0041 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02886 | hp2 | a0002 | c0005 | t0002 | g0063 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02895 | hp2 | a0002 | c0005 | t0006 | g0156 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02896 | hp1 | a0011 | c0013 | t0002 | g0151 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02896 | hp2 | a0002 | c0003 | t0003 | g0039 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02897 | hp1 | a0002 | c0003 | t0003 | g0039 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02922 | hp1 | a0002 | c0005 | t0002 | g0057 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02922 | hp2 | a0007 | c0009 | t0001 | g0005 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02965 | hp1 | a0002 | c0005 | t0010 | g0031 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02965 | hp2 | a0003 | c0004 | t0004 | g0178 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02970 | hp1 | a0002 | c0003 | t0003 | g0021 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02976 | hp1 | a0007 | c0009 | t0001 | g0028 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02976 | hp2 | a0002 | c0003 | t0003 | g0138 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03017 | hp2 | a0002 | c0010 | t0003 | g0145 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03098 | hp1 | a0002 | c0003 | t0003 | g0146 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03098 | hp2 | a0001 | c0027 | t0001 | g0002 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03130 | hp1 | a0002 | c0005 | t0010 | g0069 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03130 | hp2 | a0007 | c0009 | t0001 | g0028 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03139 | hp1 | a0007 | c0016 | t0002 | g0153 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03139 | hp2 | a0015 | c0022 | t0009 | g0159 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03195 | hp1 | a0002 | c0003 | t0003 | g0037 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03195 | hp2 | a0002 | c0005 | t0002 | g0064 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03209 | hp1 | a0003 | c0004 | t0004 | g0177 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03209 | hp2 | a0002 | c0005 | t0006 | g0117 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03225 | hp2 | a0011 | c0013 | t0002 | g0152 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03453 | hp1 | a0002 | c0003 | t0003 | g0129 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03453 | hp2 | a0002 | c0019 | t0002 | g0068 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03486 | hp1 | a0007 | c0009 | t0001 | g0028 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03486 | hp2 | a0002 | c0003 | t0003 | g0038 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03491 | hp1 | a0002 | c0005 | t0002 | g0030 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03492 | hp1 | a0002 | c0005 | t0002 | g0030 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03516 | hp1 | a0009 | c0011 | t0006 | g0061 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03516 | hp2 | a0002 | c0003 | t0003 | g0021 | AFR | ESN | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03540 | hp1 | a0009 | c0011 | t0006 | g0062 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03540 | hp2 | a0002 | c0005 | t0006 | g0040 | AFR | GWD | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03579 | hp1 | a0009 | c0011 | t0006 | g0029 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03669 | hp1 | a0005 | c0007 | t0005 | g0109 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | STU | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03704 | hp1 | a0003 | c0004 | t0004 | g0045 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03704 | hp2 | a0002 | c0030 | t0002 | g0007 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03710 | hp1 | a0005 | c0007 | t0005 | g0036 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0100 | SAS | PJL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03831 | hp1 | a0003 | c0004 | t0004 | g0168 | SAS | BEB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03942 | hp1 | a0002 | c0032 | t0002 | g0098 | SAS | BEB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0091 | SAS | BEB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG04184 | hp2 | a0005 | c0007 | t0005 | g0036 | SAS | BEB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG04199 | hp2 | a0002 | c0010 | t0003 | g0162 | SAS | STU | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG04204 | hp1 | a0002 | c0010 | t0003 | g0147 | SAS | STU | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG04204 | hp2 | a0004 | c0006 | t0002 | g0018 | SAS | STU | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | STU | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG04228 | hp2 | a0002 | c0010 | t0003 | g0132 | SAS | STU | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18522 | hp1 | a0002 | c0003 | t0003 | g0038 | AFR | YRI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | CHB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18747 | hp1 | a0002 | c0028 | t0003 | g0134 | EAS | CHB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | CHB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18906 | hp1 | a0002 | c0019 | t0002 | g0071 | AFR | YRI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18906 | hp2 | a0010 | c0026 | t0002 | g0130 | AFR | YRI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18939 | hp1 | a0004 | c0006 | t0002 | g0080 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18940 | hp2 | a0006 | c0008 | t0007 | g0054 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18947 | hp1 | a0001 | c0001 | t0015 | g0025 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18954 | hp2 | a0006 | c0008 | t0007 | g0200 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18959 | hp2 | a0006 | c0008 | t0007 | g0231 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0135 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18962 | hp2 | a0002 | c0034 | t0002 | g0099 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18967 | hp2 | a0006 | c0008 | t0007 | g0053 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18968 | hp2 | a0012 | c0014 | t0001 | g0234 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18969 | hp1 | a0002 | c0017 | t0002 | g0088 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18970 | hp1 | a0002 | c0003 | t0003 | g0139 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18970 | hp2 | a0005 | c0007 | t0005 | g0013 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18972 | hp2 | a0006 | c0008 | t0007 | g0228 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18975 | hp2 | a0012 | c0014 | t0001 | g0191 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18981 | hp2 | a0002 | c0031 | t0002 | g0066 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18982 | hp2 | a0002 | c0010 | t0003 | g0149 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18983 | hp1 | a0005 | c0007 | t0005 | g0126 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18983 | hp2 | a0006 | c0008 | t0007 | g0053 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18986 | hp2 | a0002 | c0033 | t0002 | g0020 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18989 | hp2 | a0012 | c0014 | t0001 | g0202 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18990 | hp1 | a0005 | c0007 | t0005 | g0013 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19000 | hp1 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0042 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19005 | hp2 | a0002 | c0017 | t0002 | g0089 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19010 | hp2 | a0005 | c0007 | t0005 | g0013 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19030 | hp1 | a0003 | c0004 | t0004 | g0014 | AFR | LWK | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19030 | hp2 | a0008 | c0012 | t0009 | g0160 | AFR | LWK | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19043 | hp1 | a0002 | c0029 | t0003 | g0128 | AFR | LWK | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19043 | hp2 | a0002 | c0003 | t0003 | g0133 | AFR | LWK | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19060 | hp2 | a0002 | c0003 | t0003 | g0137 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19070 | hp1 | a0006 | c0008 | t0007 | g0240 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19077 | hp1 | a0005 | c0007 | t0005 | g0123 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19083 | hp1 | a0002 | c0003 | t0003 | g0136 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19240 | hp1 | a0008 | c0012 | t0009 | g0041 | AFR | YRI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA19240 | hp2 | a0002 | c0003 | t0003 | g0114 | AFR | YRI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ASW | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA20129 | hp2 | a0002 | c0005 | t0006 | g0155 | AFR | ASW | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0082 | EUR | TSI | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01123 | hp1 | a0004 | c0006 | t0002 | g0018 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG01123 | hp2 | a0002 | c0003 | t0003 | g0148 | AMR | CLM | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02109 | hp1 | a0002 | c0005 | t0010 | g0070 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02109 | hp2 | a0002 | c0005 | t0006 | g0118 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02486 | hp1 | a0013 | c0020 | t0002 | g0060 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02486 | hp2 | a0003 | c0004 | t0004 | g0180 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02559 | hp1 | a0003 | c0004 | t0004 | g0047 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0105 | AFR | ACB | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03471 | hp1 | a0009 | c0011 | t0006 | g0029 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG03471 | hp2 | a0011 | c0013 | t0002 | g0150 | AFR | MSL | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | USA | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18955 | hp1 | a0001 | c0001 | t0008 | g0188 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA20300 | hp1 | a0002 | c0005 | t0002 | g0031 | AFR | USA | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA20300 | hp2 | a0005 | c0021 | t0002 | g0059 | AFR | USA | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA21309 | hp1 | a0002 | c0003 | t0003 | g0142 | AFR | LWK | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| NA21309 | hp2 | a0002 | c0003 | t0003 | g0140 | AFR | LWK | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0225 | REF | REF | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | CYP2F1_chr19_41109432_41133381 | CYP2F1 | chr19 | 41109432 | 41133381 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:41116202 | G | GC | 1 | a0002 | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(111): Show |
frameshift_variant | HIGH | c.15dupC | p.Thr6fs | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 2/10 | 88/1847 | 16/1476 | 6/491 | INFO_REALIGN_3_PRIME | chr19 | 41116202 | ||
| chr19:41116222 | C | T | 1 | a0002 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.34C>T | p.Leu12Phe | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 2/10 | 106/1847 | 34/1476 | 12/491 | chr19 | 41116222 | |||
| chr19:41116300 | T | C | 3 | a0005 a0009 a0013 |
22 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
missense_variant | MODERATE | c.112T>C | p.Ser38Pro | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 2/10 | 184/1847 | 112/1476 | 38/491 | chr19 | 41116300 | |||
| chr19:41116504 | G | A | 1 | a0015 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.221G>A | p.Arg74Gln | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/10 | 293/1847 | 221/1476 | 74/491 | chr19 | 41116504 | |||
| chr19:41116576 | G | A | 1 | a0015 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.293G>A | p.Arg98His | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/10 | 365/1847 | 293/1476 | 98/491 | chr19 | 41116576 | |||
| chr19:41116576 | G | C | 1 | a0014 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.293G>C | p.Arg98Pro | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/10 | 365/1847 | 293/1476 | 98/491 | chr19 | 41116576 | |||
| chr19:41121496 | G | C | 3 | a0002 a0009 a0013 |
38 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(35): Show |
missense_variant | MODERATE | c.523G>C | p.Val175Leu | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/10 | 595/1847 | 523/1476 | 175/491 | chr19 | 41121496 | |||
| chr19:41121497 | T | G | 3 | a0002 a0009 a0013 |
38 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(35): Show |
missense_variant | MODERATE | c.524T>G | p.Val175Gly | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/10 | 596/1847 | 524/1476 | 175/491 | chr19 | 41121497 | |||
| chr19:41121533 | G | A | 1 | a0012 | 3 | NA18968.hp2 NA18975.hp2 NA18989.hp2 |
missense_variant | MODERATE | c.560G>A | p.Arg187His | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/10 | 632/1847 | 560/1476 | 187/491 | chr19 | 41121533 | |||
| chr19:41121963 | G | A | 8 | a0002 a0004 a0005 others(5): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
missense_variant | MODERATE | c.652G>A | p.Asp218Asn | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/10 | 724/1847 | 652/1476 | 218/491 | chr19 | 41121963 | |||
| chr19:41122096 | G | A | 1 | a0002 | 5 | HG03017.hp2 HG04199.hp2 HG04204.hp1 others(2): Show |
missense_variant | MODERATE | c.785G>A | p.Arg262Gln | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/10 | 857/1847 | 785/1476 | 262/491 | chr19 | 41122096 | |||
| chr19:41122109 | G | C | 8 | a0002 a0004 a0007 others(5): Show |
130 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
missense_variant | MODERATE | c.798G>C | p.Gln266His | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/10 | 870/1847 | 798/1476 | 266/491 | chr19 | 41122109 | |||
| chr19:41122856 | A | G | 1 | a0002 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.857A>G | p.Asp286Gly | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/10 | 929/1847 | 857/1476 | 286/491 | chr19 | 41122856 | |||
| chr19:41125512 | T | C | 1 | a0003 | 21 | HG00741.hp2 HG01106.hp2 HG01109.hp2 others(18): Show |
missense_variant | MODERATE | c.1172T>C | p.Leu391Pro | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/10 | 1244/1847 | 1172/1476 | 391/491 | chr19 | 41125512 | |||
| chr19:41127904 | G | A | 2 | a0002 a0011 |
4 | HG02896.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
missense_variant | MODERATE | c.1298G>A | p.Arg433His | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1370/1847 | 1298/1476 | 433/491 | chr19 | 41127904 | |||
| chr19:41127922 | A | G | 1 | a0015 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1316A>G | p.Glu439Gly | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1388/1847 | 1316/1476 | 439/491 | chr19 | 41127922 | |||
| chr19:41127936 | A | C | 1 | a0002 | 35 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(32): Show |
missense_variant | MODERATE | c.1330A>C | p.Met444Leu | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1402/1847 | 1330/1476 | 444/491 | chr19 | 41127936 | |||
| chr19:41128041 | A | C | 1 | a0006 | 9 | HG02080.hp2 HG02132.hp2 NA18940.hp2 others(6): Show |
missense_variant | MODERATE | c.1435A>C | p.Asn479His | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1507/1847 | 1435/1476 | 479/491 | chr19 | 41128041 | |||
| chr19:41128050 | C | T | 1 | a0002 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.1444C>T | p.Arg482Trp | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1516/1847 | 1444/1476 | 482/491 | chr19 | 41128050 | |||
| chr19:41128072 | G | A | 3 | a0002 a0008 a0015 |
38 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(35): Show |
missense_variant | MODERATE | c.1466G>A | p.Arg489His | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1538/1847 | 1466/1476 | 489/491 | chr19 | 41128072 | |||
| chr19:41128075 | C | T | 1 | a0004 | 17 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(14): Show |
missense_variant | MODERATE | c.1469C>T | p.Pro490Leu | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1541/1847 | 1469/1476 | 490/491 | chr19 | 41128075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:41116236 | C | T | 1 | a0002c0019 | 2 | HG03453.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.48C>T | p.Val16Val | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 2/10 | 120/1847 | 48/1476 | 16/491 | chr19 | 41116236 | |||
| chr19:41116284 | G | A | 24 | a0002c0002 a0002c0003 a0002c0005 others(21): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
synonymous_variant | LOW | c.96G>A | p.Pro32Pro | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 2/10 | 168/1847 | 96/1476 | 32/491 | chr19 | 41116284 | |||
| chr19:41121591 | C | T | 4 | a0002c0003 a0002c0010 a0002c0028 others(1): Show |
33 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
synonymous_variant | LOW | c.618C>T | p.Phe206Phe | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/10 | 690/1847 | 618/1476 | 206/491 | chr19 | 41121591 | |||
| chr19:41121995 | T | C | 7 | a0002c0003 a0002c0010 a0002c0028 others(4): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
synonymous_variant | LOW | c.684T>C | p.Pro228Pro | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/10 | 756/1847 | 684/1476 | 228/491 | chr19 | 41121995 | |||
| chr19:41122001 | G | A | 1 | a0005c0021 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.690G>A | p.Pro230Pro | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/10 | 762/1847 | 690/1476 | 230/491 | chr19 | 41122001 | |||
| chr19:41122061 | C | T | 1 | a0002c0032 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.750C>T | p.His250His | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/10 | 822/1847 | 750/1476 | 250/491 | chr19 | 41122061 | |||
| chr19:41124723 | C | T | 1 | a0008c0012 | 4 | HG01884.hp2 HG02886.hp1 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.969C>T | p.Arg323Arg | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/10 | 1041/1847 | 969/1476 | 323/491 | chr19 | 41124723 | |||
| chr19:41124804 | C | T | 7 | a0002c0003 a0002c0010 a0002c0028 others(4): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
synonymous_variant | LOW | c.1050C>T | p.Asp350Asp | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/10 | 1122/1847 | 1050/1476 | 350/491 | chr19 | 41124804 | |||
| chr19:41124864 | C | T | 2 | a0007c0016 a0011c0013 |
5 | HG02615.hp2 HG02896.hp1 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.1110C>T | p.Arg370Arg | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/10 | 1182/1847 | 1110/1476 | 370/491 | chr19 | 41124864 | |||
| chr19:41125510 | C | A | 16 | a0002c0002 a0002c0005 a0002c0017 others(13): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(106): Show |
synonymous_variant | LOW | c.1170C>A | p.Thr390Thr | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/10 | 1242/1847 | 1170/1476 | 390/491 | chr19 | 41125510 | |||
| chr19:41125552 | G | A | 1 | a0002c0017 | 2 | NA18969.hp1 NA19005.hp2 |
synonymous_variant | LOW | c.1212G>A | p.Thr404Thr | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/10 | 1284/1847 | 1212/1476 | 404/491 | chr19 | 41125552 | |||
| chr19:41127926 | G | A | 1 | a0001c0027 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.1320G>A | p.Ser440Ser | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1392/1847 | 1320/1476 | 440/491 | chr19 | 41127926 | |||
| chr19:41127941 | G | A | 1 | a0002c0028 | 1 | NA18747.hp1 | synonymous_variant | LOW | c.1335G>A | p.Glu445Glu | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1407/1847 | 1335/1476 | 445/491 | chr19 | 41127941 | |||
| chr19:41128022 | A | G | 1 | a0001c0015 | 3 | HG00735.hp2 HG02155.hp1 HG02165.hp1 |
synonymous_variant | LOW | c.1416A>G | p.Pro472Pro | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 1488/1847 | 1416/1476 | 472/491 | chr19 | 41128022 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:41128120 | G | C | 1 | a0002c0002t0011 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 38 | chr19 | 41128120 | ||||||
| chr19:41128124 | G | A | 10 | a0002c0003t0003 a0002c0005t0006 a0002c0010t0003 others(7): Show |
53 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*42G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 42 | chr19 | 41128124 | ||||||
| chr19:41128131 | C | T | 8 | a0002c0003t0003 a0002c0010t0003 a0002c0018t0003 others(5): Show |
41 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*49C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 49 | chr19 | 41128131 | ||||||
| chr19:41128160 | A | G | 10 | a0002c0002t0017 a0002c0003t0003 a0002c0005t0010 others(7): Show |
45 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*78A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 78 | chr19 | 41128160 | ||||||
| chr19:41128168 | C | T | 11 | a0002c0002t0017 a0002c0003t0003 a0002c0005t0010 others(8): Show |
61 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*86C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 86 | chr19 | 41128168 | ||||||
| chr19:41128169 | T | C | 11 | a0002c0002t0017 a0002c0003t0003 a0002c0005t0010 others(8): Show |
61 | HG00558.hp2 HG00642.hp1 HG00642.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*87T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 87 | chr19 | 41128169 | ||||||
| chr19:41128196 | CCCTGCAT others(6): Show |
C | 1 | a0006c0008t0007 | 9 | HG02080.hp2 HG02132.hp2 NA18940.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*120_*132delATGCTG others(7): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 120 | INFO_REALIGN_3_PRIME | chr19 | 41128196 | |||||
| chr19:41128246 | G | A | 33 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0011 others(30): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*164G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 164 | chr19 | 41128246 | ||||||
| chr19:41128250 | C | T | 5 | a0002c0003t0003 a0002c0010t0003 a0002c0018t0003 others(2): Show |
35 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*168C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 168 | chr19 | 41128250 | ||||||
| chr19:41128324 | A | G | 36 | a0001c0001t0002 a0001c0001t0004 a0002c0002t0002 others(33): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
3_prime_UTR_variant | MODIFIER | c.*242A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 242 | chr19 | 41128324 | ||||||
| chr19:41128350 | A | AT | 25 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0015 others(22): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*270dupT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 271 | INFO_REALIGN_3_PRIME | chr19 | 41128350 | |||||
| chr19:41128351 | T | C | 2 | a0001c0001t0008 a0004c0006t0013 |
8 | HG00408.hp2 HG02056.hp2 HG02083.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*269T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 10/10 | 269 | chr19 | 41128351 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:41114505 | G | A | 30 | a0002c0005t0002g0030 a0002c0005t0002g0031 a0002c0005t0002g0057 others(27): Show |
38 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+13G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114505 | |||||||
| chr19:41114514 | G | A | 39 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(36): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.-12+22G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114514 | |||||||
| chr19:41114650 | T | G | 132 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(129): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.-12+158T>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114650 | |||||||
| chr19:41114657 | T | C | 30 | a0002c0005t0002g0030 a0002c0005t0002g0031 a0002c0005t0002g0057 others(27): Show |
38 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+165T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114657 | |||||||
| chr19:41114659 | C | T | 1 | a0006c0008t0007g0240 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-12+167C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114659 | |||||||
| chr19:41114681 | C | G | 11 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(8): Show |
17 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12+189C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114681 | |||||||
| chr19:41114770 | T | TTC | 8 | a0004c0006t0013g0074 a0005c0007t0005g0013 a0005c0007t0005g0036 others(5): Show |
12 | HG00642.hp1 HG01169.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.-12+296_-12+297dup others(2): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41114770 | ||||||
| chr19:41114770 | TTCTC | T | 10 | a0002c0005t0002g0031 a0002c0005t0010g0031 a0002c0005t0010g0069 others(7): Show |
11 | HG01884.hp2 HG02109.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-12+294_-12+297del others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41114770 | ||||||
| chr19:41114784 | CTCTCT | C | 8 | a0002c0003t0003g0158 a0002c0005t0002g0030 a0002c0005t0002g0063 others(5): Show |
9 | HG00558.hp2 HG02451.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12+294_-12+298del others(5): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41114784 | ||||||
| chr19:41114788 | C | CT | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0009 others(22): Show |
28 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12+319dupT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41114788 | ||||||
| chr19:41114788 | CT | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(30): Show |
36 | HG01070.hp2 HG02027.hp2 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.-12+319delT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41114788 | ||||||
| chr19:41114789 | T | TC | 13 | a0002c0002t0002g0107 a0004c0006t0002g0006 a0004c0006t0002g0018 others(10): Show |
19 | HG00323.hp1 HG00323.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-12+297_-12+298ins others(1): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114789 | |||||||
| chr19:41114790 | T | C | 5 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
5 | HG01069.hp1 HG01993.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+298T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114790 | |||||||
| chr19:41114791 | T | C | 3 | a0002c0003t0003g0021 a0002c0003t0003g0113 a0002c0003t0003g0114 |
5 | HG02145.hp2 HG02257.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12+299T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114791 | |||||||
| chr19:41114926 | C | T | 19 | a0002c0005t0002g0030 a0002c0005t0002g0031 a0002c0005t0002g0057 others(16): Show |
21 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12+434C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114926 | |||||||
| chr19:41114961 | G | C | 2 | a0002c0005t0002g0063 a0002c0005t0002g0064 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-12+469G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114961 | |||||||
| chr19:41114968 | C | T | 11 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(8): Show |
17 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12+476C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41114968 | |||||||
| chr19:41115013 | G | T | 1 | a0010c0023t0009g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-12+521G>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115013 | |||||||
| chr19:41115022 | G | A | 2 | a0008c0012t0009g0160 a0008c0012t0009g0161 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-12+530G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115022 | |||||||
| chr19:41115059 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00423.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-12+567C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115059 | |||||||
| chr19:41115066 | G | A | 30 | a0002c0005t0002g0030 a0002c0005t0002g0031 a0002c0005t0002g0057 others(27): Show |
38 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.-12+574G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115066 | |||||||
| chr19:41115143 | T | TTC | 2 | a0002c0005t0006g0040 a0002c0005t0006g0156 |
3 | HG01884.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-12+668_-12+669dup others(2): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41115143 | ||||||
| chr19:41115288 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | NA18972.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-12+796T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115288 | |||||||
| chr19:41115475 | C | T | 1 | a0002c0005t0006g0155 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-11-703C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115475 | |||||||
| chr19:41115515 | C | A | 1 | a0002c0005t0002g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-11-663C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115515 | |||||||
| chr19:41115537 | TGATA | T | 61 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(58): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-11-632_-11-629del others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41115537 | ||||||
| chr19:41115691 | T | TGATA | 3 | a0002c0002t0002g0081 a0002c0005t0002g0063 a0002c0005t0002g0064 |
3 | HG00099.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-11-471_-11-468dup others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41115691 | ||||||
| chr19:41115691 | TGATA | T | 13 | a0002c0002t0002g0107 a0005c0007t0005g0013 a0005c0007t0005g0036 others(10): Show |
17 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.-11-471_-11-468del others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41115691 | ||||||
| chr19:41115781 | GA | G | 19 | a0002c0005t0002g0030 a0002c0005t0002g0031 a0002c0005t0002g0057 others(16): Show |
21 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-394delA | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41115781 | ||||||
| chr19:41115786 | A | G | 19 | a0002c0005t0002g0030 a0002c0005t0002g0031 a0002c0005t0002g0057 others(16): Show |
21 | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-392A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115786 | |||||||
| chr19:41115871 | C | A | 1 | a0003c0004t0004g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-11-307C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115871 | |||||||
| chr19:41115872 | G | A | 1 | a0010c0024t0002g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-11-306G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41115872 | |||||||
| chr19:41116012 | T | A | 2 | a0001c0001t0001g0042 a0001c0001t0008g0042 |
2 | NA18968.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-11-166T>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | chr19 | 41116012 | |||||||
| chr19:41116135 | A | ATCTCACT others(6): Show |
17 | a0005c0007t0005g0013 a0005c0007t0005g0036 a0005c0007t0005g0108 others(14): Show |
22 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.-11-41_-11-40insTC others(11): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | 41116135 | ||||||
| chr19:41116362 | G | A | 17 | a0005c0007t0005g0013 a0005c0007t0005g0036 a0005c0007t0005g0108 others(14): Show |
22 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.171+3G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 2/9 | chr19 | 41116362 | |||||||
| chr19:41116710 | C | T | 39 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(36): Show |
54 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.334+93C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41116710 | |||||||
| chr19:41116756 | G | A | 1 | a0002c0002t0002g0082 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.334+139G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41116756 | |||||||
| chr19:41116959 | A | C | 5 | a0007c0016t0002g0153 a0007c0016t0002g0154 a0011c0013t0002g0150 others(2): Show |
5 | HG02615.hp2 HG02896.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.334+342A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41116959 | |||||||
| chr19:41117034 | A | G | 6 | a0002c0002t0017g0121 a0005c0021t0002g0059 a0009c0011t0006g0029 others(3): Show |
7 | HG01891.hp2 HG02486.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.334+417A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117034 | |||||||
| chr19:41117057 | C | T | 6 | a0002c0002t0017g0121 a0005c0021t0002g0059 a0009c0011t0006g0029 others(3): Show |
7 | HG01891.hp2 HG02486.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.334+440C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117057 | |||||||
| chr19:41117154 | T | C | 6 | a0002c0002t0017g0121 a0005c0021t0002g0059 a0009c0011t0006g0029 others(3): Show |
7 | HG01891.hp2 HG02486.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.334+537T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117154 | |||||||
| chr19:41117241 | C | T | 3 | a0009c0011t0006g0029 a0009c0011t0006g0061 a0009c0011t0006g0062 |
4 | HG03471.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.334+624C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117241 | |||||||
| chr19:41117266 | G | A | 1 | a0002c0029t0003g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.334+649G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117266 | |||||||
| chr19:41117284 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.334+667C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117284 | |||||||
| chr19:41117346 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.334+729G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117346 | |||||||
| chr19:41117366 | A | T | 1 | a0002c0002t0002g0106 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.334+749A>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117366 | |||||||
| chr19:41117378 | T | C | 128 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(125): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.334+761T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117378 | |||||||
| chr19:41117413 | A | C | 82 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(79): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.334+796A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117413 | |||||||
| chr19:41117449 | C | T | 4 | a0008c0012t0009g0041 a0008c0012t0009g0160 a0008c0012t0009g0161 others(1): Show |
5 | HG01884.hp2 HG02886.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.334+832C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117449 | |||||||
| chr19:41117505 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG01070.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.334+888A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117505 | |||||||
| chr19:41117536 | C | G | 27 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(24): Show |
32 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.334+919C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117536 | |||||||
| chr19:41117677 | C | T | 1 | a0002c0003t0003g0039 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.334+1060C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117677 | |||||||
| chr19:41117804 | A | G | 3 | a0009c0011t0006g0029 a0009c0011t0006g0061 a0009c0011t0006g0062 |
4 | HG03471.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.334+1187A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117804 | |||||||
| chr19:41117824 | T | A | 1 | a0010c0024t0002g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.334+1207T>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117824 | |||||||
| chr19:41117830 | C | CTTTA | 15 | a0001c0001t0001g0022 a0001c0001t0001g0044 a0001c0001t0001g0166 others(12): Show |
20 | HG00621.hp1 HG01515.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.334+1245_334+1248d others(6): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41117830 | ||||||
| chr19:41117830 | CTTTA | C | 31 | a0002c0002t0002g0131 a0002c0003t0003g0021 a0002c0003t0003g0037 others(28): Show |
37 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.334+1245_334+1248d others(6): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41117830 | ||||||
| chr19:41117830 | CTTTATTT others(1): Show |
C | 95 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(92): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.334+1241_334+1248d others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41117830 | ||||||
| chr19:41117910 | C | T | 2 | a0002c0005t0002g0030 a0002c0005t0014g0067 |
3 | HG02683.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.334+1293C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117910 | |||||||
| chr19:41117921 | C | T | 76 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(73): Show |
97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.334+1304C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117921 | |||||||
| chr19:41117936 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.334+1319G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117936 | |||||||
| chr19:41117993 | A | G | 98 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(95): Show |
126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.334+1376A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41117993 | |||||||
| chr19:41118101 | G | C | 2 | a0005c0021t0002g0059 a0013c0020t0002g0060 |
2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.334+1484G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118101 | |||||||
| chr19:41118200 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.334+1583A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118200 | |||||||
| chr19:41118220 | A | G | 13 | a0002c0005t0002g0031 a0002c0005t0006g0117 a0002c0005t0006g0118 others(10): Show |
13 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.334+1603A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118220 | |||||||
| chr19:41118254 | G | A | 1 | a0010c0023t0009g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.334+1637G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118254 | |||||||
| chr19:41118471 | G | GTACAATA others(1): Show |
15 | a0001c0001t0002g0043 a0003c0004t0004g0014 a0003c0004t0004g0045 others(12): Show |
22 | HG00741.hp2 HG01106.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.335-1858_335-1851d others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41118471 | ||||||
| chr19:41118511 | C | G | 8 | a0002c0005t0002g0030 a0002c0005t0002g0057 a0002c0005t0002g0058 others(5): Show |
9 | HG02258.hp1 HG02451.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.335-1836C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118511 | |||||||
| chr19:41118511 | C | T | 2 | a0002c0002t0002g0131 a0010c0026t0002g0130 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.335-1836C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118511 | |||||||
| chr19:41118654 | G | A | 4 | a0002c0003t0003g0021 a0002c0003t0003g0113 a0002c0003t0003g0114 others(1): Show |
6 | HG02145.hp2 HG02257.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-1693G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118654 | |||||||
| chr19:41118812 | C | T | 2 | a0007c0009t0001g0028 a0013c0020t0002g0060 |
4 | HG02486.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-1535C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118812 | |||||||
| chr19:41118866 | A | T | 3 | a0009c0011t0006g0029 a0009c0011t0006g0061 a0009c0011t0006g0062 |
4 | HG03471.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-1481A>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41118866 | |||||||
| chr19:41119229 | G | A | 5 | a0005c0021t0002g0059 a0009c0011t0006g0029 a0009c0011t0006g0061 others(2): Show |
6 | HG02486.hp1 HG03471.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-1118G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119229 | |||||||
| chr19:41119297 | C | A | 1 | a0001c0001t0001g0184 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.335-1050C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119297 | |||||||
| chr19:41119378 | C | T | 30 | a0002c0002t0002g0131 a0002c0003t0003g0021 a0002c0003t0003g0037 others(27): Show |
35 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.335-969C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119378 | |||||||
| chr19:41119474 | C | T | 5 | a0002c0005t0006g0117 a0002c0005t0006g0118 a0002c0005t0006g0119 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.335-873C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119474 | |||||||
| chr19:41119520 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.335-827G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119520 | |||||||
| chr19:41119621 | G | A | 11 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(8): Show |
17 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.335-726G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119621 | |||||||
| chr19:41119679 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.335-668C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119679 | |||||||
| chr19:41119683 | G | GTC | 7 | a0001c0001t0001g0223 a0002c0003t0003g0141 a0002c0003t0003g0142 others(4): Show |
7 | HG00642.hp2 HG00738.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.335-624_335-623dup others(2): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | G | GTCTC | 7 | a0001c0001t0001g0174 a0001c0001t0001g0224 a0002c0003t0003g0146 others(4): Show |
7 | HG02965.hp2 HG03017.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.335-626_335-623dup others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | G | GTCTCTC | 9 | a0002c0003t0003g0037 a0002c0003t0003g0148 a0002c0010t0003g0149 others(6): Show |
10 | HG01123.hp2 HG01516.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.335-628_335-623dup others(6): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | G | GTCTCTCT others(1): Show |
6 | a0002c0003t0003g0038 a0002c0003t0003g0039 a0003c0004t0004g0182 others(3): Show |
12 | HG00323.hp2 HG01106.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.335-630_335-623dup others(8): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | G | GTCTCTCT others(3): Show |
2 | a0001c0001t0001g0226 a0003c0004t0004g0183 |
2 | HG01109.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.335-632_335-623dup others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | G | GTCTCTCT others(5): Show |
3 | a0001c0001t0001g0227 a0004c0006t0002g0080 a0006c0008t0007g0228 |
3 | HG01169.hp1 NA18939.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.335-634_335-623dup others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | G | GTCTCTCT others(7): Show |
6 | a0001c0001t0001g0167 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
6 | HG01168.hp2 HG01256.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-636_335-623dup others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | G | GTCTCTCT others(9): Show |
1 | a0015c0022t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.335-638_335-623dup others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | GTC | G | 5 | a0002c0005t0006g0040 a0002c0005t0006g0156 a0002c0010t0003g0132 others(2): Show |
6 | HG01358.hp1 HG01884.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.335-624_335-623del others(2): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | GTCTC | G | 7 | a0002c0002t0002g0081 a0002c0002t0002g0094 a0002c0002t0002g0095 others(4): Show |
8 | HG00099.hp1 HG00323.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.335-626_335-623del others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | GTCTCTC | G | 8 | a0002c0002t0001g0034 a0002c0002t0002g0034 a0002c0002t0002g0035 others(5): Show |
9 | HG01081.hp2 HG01928.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.335-628_335-623del others(6): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | GTCTCTCT others(1): Show |
G | 22 | a0002c0002t0002g0003 a0002c0002t0002g0019 a0002c0002t0002g0020 others(19): Show |
33 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.335-630_335-623del others(8): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | GTCTCTCT others(3): Show |
G | 8 | a0002c0002t0002g0083 a0002c0005t0002g0031 a0002c0005t0010g0031 others(5): Show |
8 | HG00642.hp1 HG00738.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.335-632_335-623del others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119683 | GTCTCTCT others(5): Show |
G | 6 | a0002c0002t0002g0107 a0002c0018t0003g0115 a0002c0018t0003g0116 others(3): Show |
6 | HG01975.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.335-634_335-623del others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119683 | ||||||
| chr19:41119705 | C | CTCTCTCT others(4): Show |
1 | a0012c0014t0001g0234 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.335-641_335-631dup others(11): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119705 | ||||||
| chr19:41119709 | CTCTCTCT others(9): Show |
C | 1 | a0013c0020t0002g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.335-636_335-621del others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119709 | ||||||
| chr19:41119713 | C | A | 2 | a0001c0001t0001g0207 a0002c0005t0006g0040 |
2 | HG01884.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.335-634C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119713 | |||||||
| chr19:41119713 | CTCTCTCT others(5): Show |
C | 3 | a0002c0002t0002g0105 a0005c0007t0005g0013 a0005c0007t0005g0112 |
4 | HG02300.hp2 HG02559.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-632_335-621del others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119713 | ||||||
| chr19:41119715 | C | A | 4 | a0001c0001t0001g0207 a0002c0002t0002g0081 a0002c0005t0006g0040 others(1): Show |
5 | HG00099.hp1 HG01884.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.335-632C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119715 | |||||||
| chr19:41119715 | CTCTCTCT others(3): Show |
C | 5 | a0002c0002t0002g0104 a0002c0005t0006g0119 a0005c0007t0005g0013 others(2): Show |
7 | HG01175.hp2 HG01346.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.335-630_335-621del others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119715 | ||||||
| chr19:41119715 | CTCTCTCT others(5): Show |
C | 2 | a0002c0002t0002g0082 a0010c0023t0009g0157 |
2 | HG02572.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.335-630_335-619del others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119715 | ||||||
| chr19:41119717 | C | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0207 a0002c0002t0002g0081 others(6): Show |
11 | HG00099.hp1 HG01884.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.335-630C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119717 | |||||||
| chr19:41119717 | CTCTCTCT others(1): Show |
C | 8 | a0002c0002t0002g0007 a0002c0002t0002g0100 a0002c0002t0002g0102 others(5): Show |
11 | HG00438.hp2 HG00544.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.335-628_335-621del others(8): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119717 | ||||||
| chr19:41119719 | C | A | 16 | a0001c0001t0001g0050 a0001c0001t0001g0207 a0001c0001t0008g0009 others(13): Show |
18 | HG00099.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.335-628C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119719 | |||||||
| chr19:41119719 | C | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0216 |
2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.335-628C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119719 | |||||||
| chr19:41119719 | CTCTCTAT others(1): Show |
C | 3 | a0002c0030t0002g0007 a0005c0007t0005g0111 a0005c0007t0005g0125 |
3 | HG01167.hp2 HG01169.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.335-626_335-619del others(8): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119719 | ||||||
| chr19:41119721 | C | A | 33 | a0001c0001t0001g0022 a0001c0001t0001g0050 a0001c0001t0001g0207 others(30): Show |
37 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.335-626C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119721 | |||||||
| chr19:41119721 | C | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0216 |
2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.335-626C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119721 | |||||||
| chr19:41119723 | C | A | 57 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0027 others(54): Show |
65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.335-624C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119723 | |||||||
| chr19:41119723 | C | CTATATAT others(3): Show |
2 | a0001c0001t0001g0011 a0011c0013t0002g0151 |
2 | HG02896.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.335-607_335-598dup others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTATATAT others(7): Show |
1 | a0003c0004t0004g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.335-611_335-598dup others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTATATAT others(17): Show |
1 | a0001c0001t0001g0001 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.335-621_335-598dup others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTATAT others(1): Show |
3 | a0001c0001t0002g0043 a0003c0004t0004g0171 a0003c0004t0004g0212 |
3 | HG02602.hp2 HG02698.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(8): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTATAT others(3): Show |
1 | a0001c0001t0001g0004 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTATAT others(5): Show |
1 | a0003c0004t0004g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTATAT others(9): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0199 |
2 | HG01243.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTATAT others(13): Show |
1 | a0001c0001t0001g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(1): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0201 a0003c0004t0004g0014 others(1): Show |
4 | HG01243.hp1 HG02280.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(8): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(5): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0055 others(1): Show |
4 | HG00140.hp1 HG00423.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(7): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0054 a0004c0006t0002g0018 |
3 | HG01981.hp1 HG02071.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(9): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(1): Show |
5 | HG01109.hp1 HG01168.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(11): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0010 |
4 | HG01934.hp1 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(18): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(13): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0050 others(1): Show |
4 | HG02970.hp2 HG03041.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(17): Show |
1 | a0001c0001t0001g0002 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(19): Show |
2 | a0001c0001t0001g0002 a0007c0009t0001g0193 |
2 | HG02809.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(26): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(21): Show |
1 | a0001c0001t0001g0001 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(28): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTAT others(23): Show |
1 | a0001c0001t0001g0001 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(30): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCA others(12): Show |
1 | a0001c0001t0001g0205 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(19): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(3): Show |
1 | a0004c0006t0002g0072 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(5): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0051 others(3): Show |
6 | HG00741.hp1 HG01255.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(7): Show |
2 | a0001c0001t0001g0017 a0002c0003t0003g0021 |
2 | HG02145.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(9): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0042 |
3 | HG00735.hp1 NA18968.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(11): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0024 |
2 | HG01192.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(18): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(13): Show |
2 | a0001c0001t0001g0001 a0012c0014t0001g0202 |
2 | HG01192.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(17): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0190 a0001c0001t0001g0192 others(1): Show |
4 | HG00408.hp2 HG01928.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(19): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0005 |
2 | HG02897.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(26): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0005 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(28): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(3): Show |
1 | a0003c0004t0004g0014 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(5): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0166 |
2 | NA18972.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(7): Show |
4 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0173 others(1): Show |
4 | HG00621.hp1 HG01070.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(9): Show |
3 | a0001c0001t0001g0049 a0001c0001t0002g0049 a0011c0013t0002g0150 |
3 | HG02056.hp1 HG03471.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(11): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0008g0042 |
3 | NA18964.hp1 NA19002.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(18): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(13): Show |
2 | a0001c0001t0001g0208 a0014c0025t0001g0002 |
2 | HG02738.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(17): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0052 others(4): Show |
7 | HG02027.hp2 HG02165.hp2 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(19): Show |
1 | a0001c0001t0001g0001 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(26): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(25): Show |
1 | a0001c0001t0001g0163 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(32): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(27): Show |
1 | a0001c0001t0001g0002 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(34): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(5): Show |
3 | a0001c0001t0001g0008 a0002c0003t0003g0021 a0003c0004t0004g0014 |
3 | HG03516.hp2 NA19030.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(7): Show |
4 | a0001c0001t0001g0195 a0001c0001t0001g0206 a0002c0003t0003g0113 others(1): Show |
4 | HG01934.hp2 HG02257.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(9): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0002g0211 |
3 | HG01071.hp1 NA18946.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(11): Show |
1 | a0001c0027t0001g0002 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(18): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(13): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0007c0009t0001g0028 others(1): Show |
4 | HG00733.hp2 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(15): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0236 |
2 | HG01361.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(22): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(19): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0005 |
2 | HG00544.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(26): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(23): Show |
1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(30): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(27): Show |
1 | a0001c0001t0001g0026 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(34): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(7): Show |
4 | a0001c0001t0001g0015 a0001c0001t0001g0023 a0001c0001t0001g0044 others(1): Show |
4 | HG00673.hp2 HG03017.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(9): Show |
2 | a0001c0001t0001g0184 a0006c0008t0007g0053 |
2 | NA18967.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(11): Show |
1 | a0001c0001t0001g0197 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(18): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(13): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0198 |
2 | HG01346.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(15): Show |
1 | a0007c0009t0001g0028 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(22): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(17): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0164 a0007c0009t0001g0005 |
3 | HG01255.hp1 HG02630.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(19): Show |
2 | a0001c0001t0008g0008 a0012c0014t0001g0191 |
2 | HG02083.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(26): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0008 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(28): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(23): Show |
1 | a0001c0001t0001g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(30): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(9): Show |
3 | a0001c0001t0001g0017 a0004c0006t0002g0018 a0006c0008t0007g0200 |
3 | HG00280.hp2 HG04204.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(11): Show |
1 | a0001c0001t0001g0026 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(18): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(13): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0015g0025 others(1): Show |
4 | HG01106.hp1 HG03831.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(15): Show |
1 | a0007c0009t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(22): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0025 | 2 | NA18989.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(21): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0238 |
2 | NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(28): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(23): Show |
1 | a0001c0001t0001g0048 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(30): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(13): Show |
2 | a0001c0001t0001g0052 a0001c0001t0001g0186 |
2 | HG02809.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(15): Show |
1 | a0001c0001t0001g0011 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(22): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(17): Show |
2 | a0001c0001t0001g0009 a0001c0001t0001g0172 |
2 | HG02080.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.335-623_335-622ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(19): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0007c0009t0001g0005 |
3 | HG02922.hp2 NA18991.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.335-623_335-622ins others(26): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(25): Show |
1 | a0001c0001t0001g0048 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(32): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(13): Show |
1 | a0006c0008t0007g0187 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(15): Show |
1 | a0001c0001t0001g0210 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(22): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(17): Show |
1 | a0001c0001t0001g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.335-623_335-622ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(19): Show |
1 | a0001c0001t0001g0204 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(26): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(29): Show |
1 | a0001c0001t0001g0001 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(36): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTCTCT others(21): Show |
1 | a0001c0001t0001g0239 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(28): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119723 | C | CTCTTTCT others(7): Show |
1 | a0001c0001t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.335-623_335-622ins others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119723 | ||||||
| chr19:41119725 | A | C | 40 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0167 others(37): Show |
47 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.335-622A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119725 | |||||||
| chr19:41119727 | A | C | 21 | a0002c0003t0003g0037 a0002c0003t0003g0038 a0002c0003t0003g0136 others(18): Show |
27 | HG00323.hp2 HG00738.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.335-620A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119727 | |||||||
| chr19:41119729 | A | C | 9 | a0002c0003t0003g0138 a0002c0003t0003g0139 a0002c0003t0003g0140 others(6): Show |
9 | HG01106.hp2 HG01123.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.335-618A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119729 | |||||||
| chr19:41119731 | A | C | 2 | a0002c0003t0003g0140 a0002c0010t0003g0149 |
2 | NA18982.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.335-616A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119731 | |||||||
| chr19:41119733 | A | C | 1 | a0002c0010t0003g0149 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.335-614A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119733 | |||||||
| chr19:41119738 | T | C | 1 | a0002c0032t0002g0098 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.335-609T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119738 | |||||||
| chr19:41119738 | TATATATA others(15): Show |
T | 1 | a0005c0021t0002g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.335-607_335-586del others(22): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119738 | ||||||
| chr19:41119740 | T | C | 8 | a0002c0002t0002g0081 a0002c0002t0002g0094 a0002c0002t0002g0095 others(5): Show |
9 | HG00099.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.335-607T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119740 | |||||||
| chr19:41119742 | T | C | 16 | a0002c0002t0001g0034 a0002c0002t0002g0034 a0002c0002t0002g0081 others(13): Show |
17 | HG00099.hp1 HG01081.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.335-605T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119742 | |||||||
| chr19:41119744 | T | C | 45 | a0001c0001t0008g0188 a0002c0002t0001g0034 a0002c0002t0002g0003 others(42): Show |
62 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.335-603T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119744 | |||||||
| chr19:41119746 | T | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0048 others(66): Show |
91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.335-601T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119746 | |||||||
| chr19:41119748 | T | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(94): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.335-599T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119748 | |||||||
| chr19:41119748 | T | TACAC | 9 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0055 others(6): Show |
16 | HG00423.hp1 HG00621.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.335-565_335-562dup others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TACACAC | 14 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0001t0001g0054 others(11): Show |
18 | HG01070.hp1 HG01361.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.335-567_335-562dup others(6): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0184 a0001c0001t0001g0201 a0006c0008t0007g0200 |
3 | NA18954.hp2 NA19067.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.335-569_335-562dup others(8): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0230 |
3 | HG00140.hp1 HG01255.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.335-571_335-562dup others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TACACACA others(7): Show |
1 | a0015c0022t0009g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.335-575_335-562dup others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(9): Show |
1 | a0001c0001t0001g0237 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.335-598_335-597ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(5): Show |
1 | a0001c0001t0001g0185 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.335-598_335-597ins others(12): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0213 a0012c0014t0001g0234 |
2 | HG03942.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.335-598_335-597ins others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(9): Show |
2 | a0001c0001t0001g0012 a0001c0001t0004g0012 |
5 | HG00597.hp1 HG02602.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.335-598_335-597ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(11): Show |
1 | a0001c0001t0001g0214 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.335-598_335-597ins others(18): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(9): Show |
1 | a0002c0005t0002g0030 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.335-598_335-597ins others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(11): Show |
2 | a0001c0001t0001g0056 a0001c0001t0004g0215 |
3 | HG02071.hp1 NA18939.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.335-598_335-597ins others(18): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(13): Show |
2 | a0001c0001t0001g0027 a0001c0001t0004g0027 |
3 | HG01256.hp1 HG03491.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.335-598_335-597ins others(20): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(15): Show |
2 | a0001c0001t0001g0216 a0001c0001t0001g0224 |
2 | HG03688.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.335-598_335-597ins others(22): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(17): Show |
2 | a0001c0001t0001g0217 a0006c0008t0007g0240 |
2 | HG04199.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.335-598_335-597ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(17): Show |
1 | a0001c0001t0001g0218 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.335-598_335-597ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(17): Show |
1 | a0001c0015t0001g0220 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.335-598_335-597ins others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0219 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.335-598_335-597ins others(26): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(25): Show |
1 | a0001c0001t0001g0221 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.335-598_335-597ins others(32): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | T | TATATATA others(35): Show |
1 | a0001c0015t0001g0222 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.335-598_335-597ins others(42): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | TACAC | T | 7 | a0002c0003t0003g0140 a0005c0007t0005g0036 a0005c0007t0005g0109 others(4): Show |
8 | HG01167.hp2 HG01169.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.335-565_335-562del others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | TACACACA others(3): Show |
T | 1 | a0009c0011t0006g0029 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.335-571_335-562del others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119748 | TACACACA others(7): Show |
T | 1 | a0013c0020t0002g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.335-575_335-562del others(14): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr19 | 41119748 | ||||||
| chr19:41119750 | C | T | 84 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0025 others(81): Show |
113 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.335-597C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119750 | |||||||
| chr19:41119752 | C | T | 71 | a0001c0001t0001g0011 a0001c0001t0001g0042 a0001c0001t0001g0166 others(68): Show |
94 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.335-595C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119752 | |||||||
| chr19:41119754 | C | T | 41 | a0001c0001t0001g0042 a0001c0001t0001g0169 a0001c0001t0001g0233 others(38): Show |
55 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.335-593C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119754 | |||||||
| chr19:41119756 | C | T | 5 | a0001c0001t0001g0233 a0002c0003t0003g0135 a0002c0003t0003g0137 others(2): Show |
5 | HG00558.hp2 HG02615.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.335-591C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119756 | |||||||
| chr19:41119758 | C | T | 2 | a0009c0011t0006g0061 a0009c0011t0006g0062 |
2 | HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.335-589C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119758 | |||||||
| chr19:41119784 | C | T | 1 | a0003c0004t0004g0177 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.335-563C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119784 | |||||||
| chr19:41119863 | C | T | 11 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(8): Show |
17 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.335-484C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119863 | |||||||
| chr19:41119942 | A | G | 1 | a0004c0006t0002g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.335-405A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41119942 | |||||||
| chr19:41120192 | C | T | 1 | a0010c0023t0009g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.335-155C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41120192 | |||||||
| chr19:41120255 | T | C | 5 | a0005c0021t0002g0059 a0009c0011t0006g0029 a0009c0011t0006g0061 others(2): Show |
6 | HG02486.hp1 HG03471.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-92T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41120255 | |||||||
| chr19:41120316 | G | A | 1 | a0002c0019t0002g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.335-31G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41120316 | |||||||
| chr19:41120339 | C | G | 5 | a0005c0021t0002g0059 a0009c0011t0006g0029 a0009c0011t0006g0061 others(2): Show |
6 | HG02486.hp1 HG03471.hp1 HG03516.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.335-8C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 3/9 | chr19 | 41120339 | |||||||
| chr19:41120533 | CT | C | 83 | a0001c0001t0001g0167 a0001c0001t0004g0215 a0002c0002t0001g0034 others(80): Show |
105 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.484+49delT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr19 | 41120533 | ||||||
| chr19:41120826 | C | CT | 20 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(17): Show |
27 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.484+342dupT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr19 | 41120826 | ||||||
| chr19:41121003 | T | G | 13 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(10): Show |
19 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.485-455T>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121003 | |||||||
| chr19:41121014 | T | A | 25 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(22): Show |
33 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.485-444T>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121014 | |||||||
| chr19:41121018 | T | C | 53 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(50): Show |
66 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.485-440T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121018 | |||||||
| chr19:41121205 | T | C | 3 | a0009c0011t0006g0029 a0009c0011t0006g0061 a0009c0011t0006g0062 |
4 | HG03471.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-253T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121205 | |||||||
| chr19:41121254 | T | C | 41 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(38): Show |
48 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.485-204T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121254 | |||||||
| chr19:41121269 | C | T | 35 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(32): Show |
41 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.485-189C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121269 | |||||||
| chr19:41121302 | C | T | 29 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(26): Show |
34 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.485-156C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121302 | |||||||
| chr19:41121328 | C | G | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.485-130C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121328 | |||||||
| chr19:41121372 | T | A | 1 | a0001c0001t0004g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.485-86T>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121372 | |||||||
| chr19:41121378 | A | G | 29 | a0001c0001t0001g0199 a0002c0003t0003g0021 a0002c0003t0003g0037 others(26): Show |
34 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.485-80A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121378 | |||||||
| chr19:41121435 | T | C | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.485-23T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121435 | |||||||
| chr19:41121441 | G | C | 29 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(26): Show |
34 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.485-17G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121441 | |||||||
| chr19:41121444 | C | T | 29 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(26): Show |
34 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.485-14C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121444 | |||||||
| chr19:41121447 | C | T | 29 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(26): Show |
34 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.485-11C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121447 | |||||||
| chr19:41121449 | T | C | 29 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(26): Show |
34 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.485-9T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 4/9 | chr19 | 41121449 | |||||||
| chr19:41121643 | G | A | 26 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(23): Show |
34 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.645+25G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121643 | |||||||
| chr19:41121645 | A | G | 26 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(23): Show |
34 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.645+27A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121645 | |||||||
| chr19:41121648 | G | C | 26 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(23): Show |
34 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.645+30G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121648 | |||||||
| chr19:41121779 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0042 others(9): Show |
15 | HG02083.hp1 NA18612.hp1 NA18946.hp2 others(12): Show |
intron_variant | MODIFIER | c.645+161C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121779 | |||||||
| chr19:41121794 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.646-163G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121794 | |||||||
| chr19:41121801 | T | C | 45 | a0001c0001t0001g0049 a0001c0001t0002g0049 a0002c0003t0003g0021 others(42): Show |
52 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.646-156T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121801 | |||||||
| chr19:41121812 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.646-145C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121812 | |||||||
| chr19:41121843 | G | GCCTCTCC others(3): Show |
35 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(32): Show |
41 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.646-114_646-113ins others(10): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121843 | |||||||
| chr19:41121858 | T | G | 35 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(32): Show |
41 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.646-99T>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121858 | |||||||
| chr19:41121917 | T | C | 16 | a0002c0002t0002g0032 a0002c0002t0002g0081 a0002c0002t0002g0082 others(13): Show |
21 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.646-40T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 5/9 | chr19 | 41121917 | |||||||
| chr19:41122178 | C | T | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.822+45C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122178 | |||||||
| chr19:41122207 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.822+74G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122207 | |||||||
| chr19:41122234 | A | T | 1 | a0003c0004t0004g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.822+101A>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122234 | |||||||
| chr19:41122293 | C | T | 2 | a0001c0001t0001g0163 a0001c0001t0001g0165 |
2 | HG02083.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.822+160C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122293 | |||||||
| chr19:41122398 | G | A | 4 | a0002c0002t0002g0019 a0002c0002t0002g0084 a0002c0002t0002g0085 others(1): Show |
6 | HG00621.hp2 NA18612.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+265G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122398 | |||||||
| chr19:41122420 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.822+287C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122420 | |||||||
| chr19:41122439 | C | T | 1 | a0002c0010t0003g0149 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.822+306C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122439 | |||||||
| chr19:41122444 | C | G | 1 | a0001c0001t0001g0194 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.822+311C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122444 | |||||||
| chr19:41122499 | C | T | 5 | a0002c0005t0006g0117 a0002c0005t0006g0118 a0002c0005t0006g0119 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.823-323C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122499 | |||||||
| chr19:41122503 | TACATACA others(21): Show |
T | 1 | a0010c0024t0002g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.823-303_823-276del others(28): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr19 | 41122503 | ||||||
| chr19:41122527 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.823-295T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122527 | |||||||
| chr19:41122531 | CACAT | C | 3 | a0009c0011t0006g0029 a0009c0011t0006g0061 a0009c0011t0006g0062 |
4 | HG03471.hp1 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-278_823-275del others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr19 | 41122531 | ||||||
| chr19:41122547 | TCATACAT others(9): Show |
T | 1 | a0010c0023t0009g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823-246_823-231del others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr19 | 41122547 | ||||||
| chr19:41122715 | A | C | 1 | a0010c0023t0009g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.823-107A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122715 | |||||||
| chr19:41122772 | T | G | 77 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(74): Show |
98 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.823-50T>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122772 | |||||||
| chr19:41122776 | G | T | 4 | a0002c0002t0002g0019 a0002c0002t0002g0084 a0002c0002t0002g0085 others(1): Show |
6 | HG00621.hp2 NA18612.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-46G>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122776 | |||||||
| chr19:41122783 | C | A | 1 | a0003c0004t0004g0168 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.823-39C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 6/9 | chr19 | 41122783 | |||||||
| chr19:41123072 | A | G | 1 | a0005c0021t0002g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.964+109A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123072 | |||||||
| chr19:41123110 | G | A | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.964+147G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123110 | |||||||
| chr19:41123113 | C | T | 1 | a0002c0002t0002g0107 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.964+150C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123113 | |||||||
| chr19:41123153 | C | T | 1 | a0002c0029t0003g0128 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.964+190C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123153 | |||||||
| chr19:41123221 | G | A | 1 | a0010c0023t0009g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.964+258G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123221 | |||||||
| chr19:41123257 | G | A | 16 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(13): Show |
22 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.964+294G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123257 | |||||||
| chr19:41123294 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.964+331C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123294 | |||||||
| chr19:41123317 | TCAGCCTC others(17): Show |
T | 1 | a0001c0001t0001g0048 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.964+381_964+404del others(24): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr19 | 41123317 | ||||||
| chr19:41123330 | T | C | 2 | a0002c0002t0002g0131 a0010c0026t0002g0130 |
2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.964+367T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123330 | |||||||
| chr19:41123582 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.964+619C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123582 | |||||||
| chr19:41123634 | G | A | 1 | a0010c0024t0002g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.964+671G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123634 | |||||||
| chr19:41123637 | T | C | 11 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(8): Show |
17 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.964+674T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123637 | |||||||
| chr19:41123751 | T | G | 1 | a0002c0002t0002g0106 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.964+788T>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123751 | |||||||
| chr19:41123770 | C | A | 2 | a0005c0007t0005g0036 a0005c0007t0005g0109 |
3 | HG03669.hp1 HG03710.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.964+807C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123770 | |||||||
| chr19:41123882 | G | A | 28 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(25): Show |
33 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.965-837G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123882 | |||||||
| chr19:41123891 | G | A | 1 | a0002c0003t0003g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.965-828G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123891 | |||||||
| chr19:41123990 | C | T | 13 | a0002c0005t0002g0031 a0002c0005t0006g0117 a0002c0005t0006g0118 others(10): Show |
13 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.965-729C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41123990 | |||||||
| chr19:41124008 | G | A | 2 | a0002c0005t0006g0040 a0002c0005t0006g0156 |
3 | HG01884.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.965-711G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124008 | |||||||
| chr19:41124056 | C | T | 2 | a0002c0005t0002g0063 a0002c0005t0002g0064 |
2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.965-663C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124056 | |||||||
| chr19:41124108 | A | G | 7 | a0002c0003t0003g0037 a0002c0003t0003g0038 a0002c0003t0003g0141 others(4): Show |
9 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-611A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124108 | |||||||
| chr19:41124128 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.965-591C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124128 | |||||||
| chr19:41124142 | T | C | 4 | a0002c0002t0002g0019 a0002c0002t0002g0084 a0002c0002t0002g0085 others(1): Show |
6 | HG00621.hp2 NA18612.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.965-577T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124142 | |||||||
| chr19:41124143 | G | A | 4 | a0002c0002t0002g0019 a0002c0002t0002g0084 a0002c0002t0002g0085 others(1): Show |
6 | HG00621.hp2 NA18612.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.965-576G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124143 | |||||||
| chr19:41124227 | CT | C | 52 | a0001c0001t0001g0224 a0002c0003t0003g0021 a0002c0003t0003g0037 others(49): Show |
64 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.965-480delT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr19 | 41124227 | ||||||
| chr19:41124243 | C | CT | 19 | a0002c0003t0003g0133 a0002c0003t0003g0138 a0002c0003t0003g0139 others(16): Show |
25 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.965-474dupT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr19 | 41124243 | ||||||
| chr19:41124243 | CT | C | 2 | a0002c0018t0003g0115 a0003c0004t0004g0046 |
3 | HG01516.hp2 HG01517.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.965-474delT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr19 | 41124243 | ||||||
| chr19:41124245 | T | C | 4 | a0002c0002t0002g0081 a0003c0004t0004g0045 a0003c0004t0004g0181 others(1): Show |
5 | HG00099.hp1 HG00741.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.965-474T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124245 | |||||||
| chr19:41124245 | T | TTC | 8 | a0002c0003t0003g0037 a0002c0003t0003g0038 a0002c0003t0003g0039 others(5): Show |
11 | HG00642.hp2 HG00738.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.965-474_965-473ins others(2): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124245 | |||||||
| chr19:41124245 | T | TTCC | 3 | a0002c0003t0003g0144 a0002c0003t0003g0146 a0002c0003t0003g0148 |
3 | HG01123.hp2 HG02818.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.965-474_965-473ins others(3): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124245 | |||||||
| chr19:41124246 | C | T | 17 | a0002c0003t0003g0021 a0002c0003t0003g0113 a0002c0003t0003g0114 others(14): Show |
19 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.965-473C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124246 | |||||||
| chr19:41124251 | C | G | 1 | a0002c0003t0003g0114 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.965-468C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124251 | |||||||
| chr19:41124252 | C | G | 1 | a0002c0002t0002g0092 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.965-467C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124252 | |||||||
| chr19:41124253 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.965-466C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124253 | |||||||
| chr19:41124253 | C | G | 1 | a0001c0001t0008g0188 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.965-466C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124253 | |||||||
| chr19:41124253 | C | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0206 a0001c0001t0001g0208 others(4): Show |
9 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-466C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124253 | |||||||
| chr19:41124254 | C | A | 10 | a0001c0001t0001g0050 a0001c0001t0001g0192 a0001c0001t0001g0203 others(7): Show |
11 | NA18940.hp1 NA18968.hp2 NA18971.hp1 others(8): Show |
intron_variant | MODIFIER | c.965-465C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124254 | |||||||
| chr19:41124255 | CT | C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(86): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.965-438delT | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr19 | 41124255 | ||||||
| chr19:41124255 | CTT | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0025 others(42): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.965-439_965-438del others(2): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr19 | 41124255 | ||||||
| chr19:41124255 | CTTT | C | 14 | a0001c0001t0001g0042 a0001c0001t0002g0211 a0001c0001t0008g0042 others(11): Show |
15 | HG00558.hp1 HG02155.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.965-440_965-438del others(3): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr19 | 41124255 | ||||||
| chr19:41124255 | CTTTT | C | 7 | a0002c0002t0002g0087 a0002c0005t0002g0057 a0002c0005t0002g0058 others(4): Show |
7 | HG02258.hp1 HG02683.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.965-441_965-438del others(4): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr19 | 41124255 | ||||||
| chr19:41124256 | T | A | 12 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(9): Show |
18 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.965-463T>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124256 | |||||||
| chr19:41124256 | T | C | 52 | a0001c0001t0001g0004 a0001c0001t0001g0199 a0001c0001t0002g0043 others(49): Show |
66 | HG00642.hp1 HG00741.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.965-463T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124256 | |||||||
| chr19:41124256 | T | TC | 11 | a0002c0003t0003g0037 a0002c0003t0003g0038 a0002c0003t0003g0039 others(8): Show |
14 | HG00642.hp2 HG00738.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.965-463_965-462ins others(1): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124256 | |||||||
| chr19:41124257 | T | A | 5 | a0007c0016t0002g0153 a0007c0016t0002g0154 a0011c0013t0002g0150 others(2): Show |
5 | HG02615.hp2 HG02896.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-462T>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124257 | |||||||
| chr19:41124257 | T | C | 60 | a0002c0002t0002g0033 a0002c0002t0002g0085 a0002c0002t0002g0086 others(57): Show |
76 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.965-462T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124257 | |||||||
| chr19:41124257 | T | TCC | 12 | a0002c0003t0003g0021 a0002c0003t0003g0113 a0002c0003t0003g0114 others(9): Show |
14 | HG02145.hp2 HG02257.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.965-462_965-461ins others(2): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124257 | |||||||
| chr19:41124258 | T | C | 41 | a0001c0001t0001g0165 a0002c0002t0002g0003 a0002c0002t0002g0007 others(38): Show |
55 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.965-461T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124258 | |||||||
| chr19:41124259 | T | C | 10 | a0002c0002t0001g0034 a0002c0002t0002g0020 a0002c0002t0002g0034 others(7): Show |
11 | HG00558.hp1 HG02135.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.965-460T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124259 | |||||||
| chr19:41124260 | T | C | 1 | a0002c0002t0002g0087 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.965-459T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124260 | |||||||
| chr19:41124303 | A | G | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.965-416A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124303 | |||||||
| chr19:41124343 | A | C | 5 | a0007c0016t0002g0153 a0007c0016t0002g0154 a0011c0013t0002g0150 others(2): Show |
5 | HG02615.hp2 HG02896.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-376A>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124343 | |||||||
| chr19:41124506 | C | A | 42 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(39): Show |
57 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.965-213C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124506 | |||||||
| chr19:41124684 | G | A | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.965-35G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124684 | |||||||
| chr19:41124711 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0205 a0001c0001t0001g0207 |
3 | NA18971.hp1 NA18973.hp2 NA18990.hp2 |
splice_region_variant&intron_variant | LOW | c.965-8C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 7/9 | chr19 | 41124711 | |||||||
| chr19:41124955 | G | C | 1 | a0011c0013t0002g0151 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1152+49G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/9 | chr19 | 41124955 | |||||||
| chr19:41125105 | G | C | 2 | a0001c0001t0001g0173 a0001c0001t0004g0215 |
2 | HG02698.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.1152+199G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/9 | chr19 | 41125105 | |||||||
| chr19:41125125 | A | G | 27 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(24): Show |
32 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1152+219A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/9 | chr19 | 41125125 | |||||||
| chr19:41125152 | C | T | 1 | a0002c0003t0003g0136 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1152+246C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/9 | chr19 | 41125152 | |||||||
| chr19:41125251 | T | C | 16 | a0001c0001t0002g0043 a0003c0004t0004g0014 a0003c0004t0004g0045 others(13): Show |
23 | HG00741.hp2 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1153-242T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/9 | chr19 | 41125251 | |||||||
| chr19:41125263 | T | G | 20 | a0001c0001t0002g0043 a0003c0004t0004g0014 a0003c0004t0004g0045 others(17): Show |
28 | HG00741.hp2 HG01106.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1153-230T>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/9 | chr19 | 41125263 | |||||||
| chr19:41125427 | A | G | 3 | a0008c0012t0009g0041 a0008c0012t0009g0160 a0008c0012t0009g0161 |
4 | HG01884.hp2 HG02886.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1153-66A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 8/9 | chr19 | 41125427 | |||||||
| chr19:41125687 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1294+53C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41125687 | |||||||
| chr19:41125788 | G | A | 1 | a0011c0013t0002g0152 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1294+154G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41125788 | |||||||
| chr19:41125811 | G | A | 28 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(25): Show |
38 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1294+177G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41125811 | |||||||
| chr19:41125820 | G | A | 1 | a0013c0020t0002g0060 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1294+186G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41125820 | |||||||
| chr19:41125917 | G | A | 1 | a0003c0004t0004g0179 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1294+283G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41125917 | |||||||
| chr19:41126022 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1294+388A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126022 | |||||||
| chr19:41126056 | C | A | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1294+422C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126056 | |||||||
| chr19:41126109 | C | T | 5 | a0002c0010t0003g0132 a0002c0010t0003g0145 a0002c0010t0003g0147 others(2): Show |
5 | HG03017.hp2 HG04199.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.1294+475C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126109 | |||||||
| chr19:41126153 | C | A | 1 | a0005c0021t0002g0059 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1294+519C>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126153 | |||||||
| chr19:41126154 | A | G | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1294+520A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126154 | |||||||
| chr19:41126202 | G | A | 52 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(49): Show |
68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1294+568G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126202 | |||||||
| chr19:41126333 | G | A | 50 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(47): Show |
66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1294+699G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126333 | |||||||
| chr19:41126411 | A | G | 85 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(82): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.1294+777A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126411 | |||||||
| chr19:41126539 | G | T | 11 | a0004c0006t0002g0006 a0004c0006t0002g0018 a0004c0006t0002g0072 others(8): Show |
17 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1294+905G>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126539 | |||||||
| chr19:41126618 | G | A | 2 | a0002c0005t0006g0040 a0002c0005t0006g0156 |
3 | HG01884.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1294+984G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126618 | |||||||
| chr19:41126629 | C | G | 2 | a0002c0005t0006g0040 a0002c0005t0006g0156 |
3 | HG01884.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1294+995C>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126629 | |||||||
| chr19:41126632 | T | C | 52 | a0002c0002t0001g0034 a0002c0002t0002g0003 a0002c0002t0002g0007 others(49): Show |
68 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1294+998T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126632 | |||||||
| chr19:41126853 | G | T | 32 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(29): Show |
38 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1295-1048G>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126853 | |||||||
| chr19:41126900 | G | C | 28 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(25): Show |
33 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1295-1001G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41126900 | |||||||
| chr19:41127075 | T | C | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1295-826T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127075 | |||||||
| chr19:41127094 | G | A | 2 | a0002c0017t0002g0088 a0002c0017t0002g0089 |
2 | NA18969.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1295-807G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127094 | |||||||
| chr19:41127136 | T | C | 18 | a0002c0005t0002g0031 a0002c0005t0006g0040 a0002c0005t0006g0117 others(15): Show |
20 | HG01884.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1295-765T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127136 | |||||||
| chr19:41127211 | GTTGTTAG others(7): Show |
G | 1 | a0010c0024t0002g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1295-688_1295-675d others(16): Show |
CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr19 | 41127211 | ||||||
| chr19:41127216 | T | C | 1 | a0010c0023t0009g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1295-685T>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127216 | |||||||
| chr19:41127447 | C | T | 1 | a0002c0002t0002g0103 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1295-454C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127447 | |||||||
| chr19:41127463 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0042 a0001c0001t0001g0166 others(5): Show |
9 | NA18946.hp2 NA18947.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.1295-438G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127463 | |||||||
| chr19:41127524 | G | A | 1 | a0006c0008t0007g0053 | 2 | NA18967.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1295-377G>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127524 | |||||||
| chr19:41127554 | A | T | 12 | a0005c0007t0005g0013 a0005c0007t0005g0036 a0005c0007t0005g0108 others(9): Show |
16 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1295-347A>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127554 | |||||||
| chr19:41127641 | C | T | 1 | a0010c0023t0009g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1295-260C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127641 | |||||||
| chr19:41127662 | C | T | 12 | a0005c0007t0005g0013 a0005c0007t0005g0036 a0005c0007t0005g0108 others(9): Show |
16 | HG00642.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1295-239C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127662 | |||||||
| chr19:41127731 | C | T | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1295-170C>T | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127731 | |||||||
| chr19:41127737 | A | G | 2 | a0002c0005t0002g0030 a0002c0005t0014g0067 |
3 | HG02683.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1295-164A>G | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127737 | |||||||
| chr19:41127764 | G | C | 5 | a0007c0016t0002g0153 a0007c0016t0002g0154 a0011c0013t0002g0150 others(2): Show |
5 | HG02615.hp2 HG02896.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-137G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127764 | |||||||
| chr19:41127765 | T | A | 5 | a0007c0016t0002g0153 a0007c0016t0002g0154 a0011c0013t0002g0150 others(2): Show |
5 | HG02615.hp2 HG02896.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-136T>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127765 | |||||||
| chr19:41127810 | T | A | 33 | a0002c0003t0003g0021 a0002c0003t0003g0037 a0002c0003t0003g0038 others(30): Show |
39 | HG00558.hp2 HG00642.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1295-91T>A | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127810 | |||||||
| chr19:41127842 | G | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0206 a0001c0001t0001g0226 others(3): Show |
8 | HG01070.hp2 HG01071.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1295-59G>C | CYP2F1 | ENSG00000197446.9 | transcript | ENST00000331105.7 | protein_coding | 9/9 | chr19 | 41127842 |