Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 260293 |
| ensemblid | ENSG00000186377.8 |
| hgncid | 20244 |
| symbol | CYP4X1 |
| name | cytochrome P450 family 4 subfamily X member 1 |
| refseq_nuc | NM_178033.2 |
| refseq_prot | NP_828847.1 |
| ensembl_nuc | ENST00000371901.4 |
| ensembl_prot | ENSP00000360968.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 47023669 |
| end | 47050751 |
| strand | + |
| ver | v1.2 |
| region | chr1:47023669-47050751 |
| region5000 | chr1:47018669-47055751 |
| regionname0 | CYP4X1_chr1_47023669_47050751 |
| regionname5000 | CYP4X1_chr1_47018669_47055751 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 509 | 346 | 89 | 70 | 135 | 14 | 36 | 102 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | MEFSW others(504): Show |
chr1 | 47018669 | 47055751 |
| a0002 | 0/0 | 509 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | MEFSW others(504): Show |
chr1 | 47018669 | 47055751 |
| a0003 | 0/0 | 509 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | MEFSW others(504): Show |
chr1 | 47018669 | 47055751 |
| a0004 | 0/0 | 509 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | MEFSW others(504): Show |
chr1 | 47018669 | 47055751 |
| a0005 | 0/0 | 509 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | MEFSW others(504): Show |
chr1 | 47018669 | 47055751 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1527 | 342 | 87 | 69 | 134 | 14 | 36 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ATGGA others(1522): Show |
chr1 | 47018669 | 47055751 | ||
| a0001c0002 | 0/0 | 1527 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ATGGA others(1522): Show |
chr1 | 47018669 | 47055751 | ||
| a0001c0005 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ATGGA others(1522): Show |
chr1 | 47018669 | 47055751 | ||
| a0001c0006 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ATGGA others(1522): Show |
chr1 | 47018669 | 47055751 | ||
| a0002c0004 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ATGGA others(1522): Show |
chr1 | 47018669 | 47055751 | ||
| a0003c0007 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ATGGA others(1522): Show |
chr1 | 47018669 | 47055751 | ||
| a0004c0003 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ATGGA others(1522): Show |
chr1 | 47018669 | 47055751 | ||
| a0005c0008 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ATGGA others(1522): Show |
chr1 | 47018669 | 47055751 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2256 | 332 | 78 | 68 | 134 | 14 | 36 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0001c0001t0002 | 0/0 | 2256 | 5 | 4 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0001c0001t0003 | 0/0 | 2256 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0001c0001t0005 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0001c0002t0004 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0001c0005t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0001c0006t0001 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0002c0004t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0003c0007t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0004c0003t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| a0005c0008t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | ACTGC others(2251): Show |
chr1 | 47018669 | 47055751 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 48 | 17 | 20 | 2 | 5 | 4 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0002 | 0/0 | 14 | 0 | 1 | 8 | 1 | 4 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0003 | 0/0 | 10 | 1 | 1 | 8 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0004 | 0/0 | 10 | 1 | 2 | 6 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0005 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0006 | 0/0 | 9 | 1 | 2 | 2 | 3 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0007 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0008 | 0/0 | 8 | 0 | 1 | 6 | 1 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0011 | 0/0 | 6 | 1 | 1 | 2 | 0 | 2 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0012 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0013 | 0/0 | 6 | 0 | 5 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0014 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0020 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0043 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0002g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0002t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0002t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0005t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0001c0006t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0002c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0003c0007t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0004c0003t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| a0005c0008t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00438 | hp1 | a0002 | c0004 | t0001 | g0132 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01243 | hp1 | a0001 | c0006 | t0001 | g0029 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01884 | hp1 | a0003 | c0007 | t0001 | g0099 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01891 | hp1 | a0004 | c0003 | t0001 | g0001 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CDX | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02155 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | CDX | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03041 | hp1 | a0005 | c0008 | t0001 | g0167 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0096 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | STU | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ASW | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0095 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | LWK | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0043 | REF | REF | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0020 | REF | REF | CYP4X1_chr1_47018669_47055751 | CYP4X1 | chr1 | 47018669 | 47055751 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47030030 | T | C | 1 | a0004 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.218T>C | p.Ile73Thr | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/12 | 367/2256 | 218/1530 | 73/509 | chr1 | 47030030 | |||
| chr1:47033253 | C | T | 1 | a0005 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.377C>T | p.Ala126Val | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/12 | 526/2256 | 377/1530 | 126/509 | chr1 | 47033253 | |||
| chr1:47036040 | C | G | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.644C>G | p.Ala215Gly | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/12 | 793/2256 | 644/1530 | 215/509 | chr1 | 47036040 | |||
| chr1:47036120 | C | A | 1 | a0002 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.724C>A | p.Pro242Thr | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/12 | 873/2256 | 724/1530 | 242/509 | chr1 | 47036120 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47038664 | A | G | 1 | a0001c0006 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.780A>G | p.Thr260Thr | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 7/12 | 929/2256 | 780/1530 | 260/509 | chr1 | 47038664 | |||
| chr1:47046539 | G | C | 1 | a0001c0002 | 2 | HG02486.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.1146G>C | p.Pro382Pro | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/12 | 1295/2256 | 1146/1530 | 382/509 | chr1 | 47046539 | |||
| chr1:47050159 | A | G | 1 | a0001c0005 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.1515A>G | p.Lys505Lys | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 12/12 | 1664/2256 | 1515/1530 | 505/509 | chr1 | 47050159 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47023751 | G | A | 1 | a0001c0001t0002 | 5 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/12 | 67 | chr1 | 47023751 | ||||||
| chr1:47050450 | T | C | 1 | a0001c0002t0004 | 2 | HG02486.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*276T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 12/12 | 276 | chr1 | 47050450 | ||||||
| chr1:47050567 | C | T | 2 | a0001c0001t0003 a0001c0001t0005 |
5 | HG02572.hp2 HG02615.hp2 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*393C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 12/12 | 393 | chr1 | 47050567 | ||||||
| chr1:47050610 | C | T | 1 | a0001c0001t0005 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*436C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 12/12 | 436 | chr1 | 47050610 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47024114 | T | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(82): Show |
168 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.177+120T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47024114 | |||||||
| chr1:47024123 | C | CT | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
4 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+129_177+130ins others(1): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47024123 | |||||||
| chr1:47024124 | A | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
4 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+130A>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47024124 | |||||||
| chr1:47024406 | C | A | 1 | a0001c0001t0003g0107 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.177+412C>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47024406 | |||||||
| chr1:47024583 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.177+589A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47024583 | |||||||
| chr1:47024635 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.177+641T>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47024635 | |||||||
| chr1:47024714 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.177+720C>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47024714 | |||||||
| chr1:47024900 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.177+906T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47024900 | |||||||
| chr1:47025072 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0165 others(5): Show |
10 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.177+1078A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025072 | |||||||
| chr1:47025147 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
4 | HG00673.hp2 NA18979.hp2 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+1153T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025147 | |||||||
| chr1:47025168 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.177+1174C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025168 | |||||||
| chr1:47025193 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG02818.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.177+1199A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025193 | |||||||
| chr1:47025211 | G | T | 2 | a0001c0001t0003g0163 a0001c0001t0003g0164 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.177+1217G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025211 | |||||||
| chr1:47025302 | C | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
223 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.177+1308C>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025302 | |||||||
| chr1:47025517 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.177+1523G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025517 | |||||||
| chr1:47025686 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.177+1692A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025686 | |||||||
| chr1:47025688 | T | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(125): Show |
245 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.177+1694T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025688 | |||||||
| chr1:47025721 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.177+1727T>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025721 | |||||||
| chr1:47025722 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.177+1728C>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025722 | |||||||
| chr1:47025900 | A | G | 2 | a0001c0002t0004g0095 a0001c0002t0004g0096 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.177+1906A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025900 | |||||||
| chr1:47025974 | A | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(75): Show |
157 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.177+1980A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47025974 | |||||||
| chr1:47026082 | G | C | 1 | a0001c0001t0001g0024 | 2 | HG02040.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.177+2088G>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026082 | |||||||
| chr1:47026122 | A | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
217 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.177+2128A>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026122 | |||||||
| chr1:47026122 | A | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(15): Show |
28 | HG00280.hp2 HG00408.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.177+2128A>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026122 | |||||||
| chr1:47026185 | G | C | 1 | a0001c0001t0001g0017 | 3 | HG02132.hp2 HG02523.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.177+2191G>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026185 | |||||||
| chr1:47026198 | A | C | 1 | a0001c0001t0005g0160 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.177+2204A>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026198 | |||||||
| chr1:47026295 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02922.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.177+2301G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026295 | |||||||
| chr1:47026328 | A | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0155 a0001c0001t0001g0156 others(3): Show |
7 | HG02280.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+2334A>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026328 | |||||||
| chr1:47026745 | T | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0039 others(21): Show |
77 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.177+2751T>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026745 | |||||||
| chr1:47026779 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.177+2785G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026779 | |||||||
| chr1:47026916 | C | T | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.177+2922C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026916 | |||||||
| chr1:47026989 | A | G | 2 | a0001c0002t0004g0095 a0001c0002t0004g0096 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.177+2995A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026989 | |||||||
| chr1:47026991 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.177+2997A>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47026991 | |||||||
| chr1:47027011 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.178-2979G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027011 | |||||||
| chr1:47027036 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.178-2954T>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027036 | |||||||
| chr1:47027121 | T | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
152 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.178-2869T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027121 | |||||||
| chr1:47027168 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.178-2822C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027168 | |||||||
| chr1:47027250 | A | G | 1 | a0002c0004t0001g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.178-2740A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027250 | |||||||
| chr1:47027327 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.178-2663G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027327 | |||||||
| chr1:47027371 | G | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(11): Show |
24 | HG00280.hp2 HG00408.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.178-2619G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027371 | |||||||
| chr1:47027666 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.178-2324A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027666 | |||||||
| chr1:47027675 | A | G | 2 | a0001c0002t0004g0095 a0001c0002t0004g0096 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.178-2315A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027675 | |||||||
| chr1:47027746 | A | T | 2 | a0001c0001t0001g0029 a0001c0006t0001g0029 |
2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.178-2244A>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027746 | |||||||
| chr1:47027752 | G | A | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.178-2238G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027752 | |||||||
| chr1:47027829 | G | C | 1 | a0001c0001t0002g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.178-2161G>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027829 | |||||||
| chr1:47027912 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
219 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.178-2078A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47027912 | |||||||
| chr1:47028006 | C | T | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.178-1984C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47028006 | |||||||
| chr1:47028183 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.178-1807T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47028183 | |||||||
| chr1:47028291 | G | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG02129.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.178-1699G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47028291 | |||||||
| chr1:47028685 | C | T | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.178-1305C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47028685 | |||||||
| chr1:47029112 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.178-878G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47029112 | |||||||
| chr1:47029362 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.178-628C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47029362 | |||||||
| chr1:47029497 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.178-493G>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47029497 | |||||||
| chr1:47029604 | T | A | 2 | a0001c0002t0004g0095 a0001c0002t0004g0096 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.178-386T>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47029604 | |||||||
| chr1:47029705 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.178-285G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47029705 | |||||||
| chr1:47029862 | G | A | 1 | a0001c0001t0001g0032 | 2 | NA19007.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.178-128G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47029862 | |||||||
| chr1:47029933 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.178-57A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47029933 | |||||||
| chr1:47029940 | G | A | 1 | a0001c0001t0001g0016 | 5 | HG02145.hp2 HG02486.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.178-50G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 1/11 | chr1 | 47029940 | |||||||
| chr1:47030150 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.319+19C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47030150 | |||||||
| chr1:47030193 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.319+62T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47030193 | |||||||
| chr1:47030260 | T | C | 2 | a0001c0002t0004g0095 a0001c0002t0004g0096 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319+129T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47030260 | |||||||
| chr1:47030430 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02922.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.319+299G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47030430 | |||||||
| chr1:47030727 | A | G | 2 | a0001c0002t0004g0095 a0001c0002t0004g0096 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.319+596A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47030727 | |||||||
| chr1:47030810 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.320-626A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47030810 | |||||||
| chr1:47030848 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.320-588G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47030848 | |||||||
| chr1:47031066 | A | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.320-370A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47031066 | |||||||
| chr1:47031201 | A | T | 2 | a0001c0001t0001g0029 a0001c0006t0001g0029 |
2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.320-235A>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47031201 | |||||||
| chr1:47031311 | C | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
178 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.320-125C>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47031311 | |||||||
| chr1:47031365 | G | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.320-71G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47031365 | |||||||
| chr1:47031403 | G | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0166 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.320-33G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 2/11 | chr1 | 47031403 | |||||||
| chr1:47031545 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.364+65A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47031545 | |||||||
| chr1:47031620 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.364+140G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47031620 | |||||||
| chr1:47031740 | C | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG01070.hp2 HG01081.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.364+260C>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47031740 | |||||||
| chr1:47031787 | A | G | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.364+307A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47031787 | |||||||
| chr1:47031800 | G | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.364+320G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47031800 | |||||||
| chr1:47032056 | CA | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
68 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.364+586delA | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 47032056 | ||||||
| chr1:47032081 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.364+601G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47032081 | |||||||
| chr1:47032133 | G | A | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.364+653G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47032133 | |||||||
| chr1:47032884 | A | G | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.365-357A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47032884 | |||||||
| chr1:47032907 | G | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.365-334G>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47032907 | |||||||
| chr1:47032978 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.365-263G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47032978 | |||||||
| chr1:47033165 | G | A | 2 | a0001c0001t0001g0029 a0001c0006t0001g0029 |
2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.365-76G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 3/11 | chr1 | 47033165 | |||||||
| chr1:47033401 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.492+33C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47033401 | |||||||
| chr1:47033622 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.492+254G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47033622 | |||||||
| chr1:47033660 | T | G | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.492+292T>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47033660 | |||||||
| chr1:47033668 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0001g0165 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.492+300G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47033668 | |||||||
| chr1:47033707 | G | A | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.492+339G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47033707 | |||||||
| chr1:47033826 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0166 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.492+458C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47033826 | |||||||
| chr1:47034123 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
262 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.492+755C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034123 | |||||||
| chr1:47034239 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.492+871A>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034239 | |||||||
| chr1:47034326 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.492+958T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034326 | |||||||
| chr1:47034337 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(121): Show |
241 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.492+969T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034337 | |||||||
| chr1:47034651 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.493-1155C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034651 | |||||||
| chr1:47034793 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.493-1013A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034793 | |||||||
| chr1:47034799 | C | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(30): Show |
61 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.493-1007C>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034799 | |||||||
| chr1:47034805 | G | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.493-1001G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034805 | |||||||
| chr1:47034891 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
267 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.493-915T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034891 | |||||||
| chr1:47034914 | T | G | 2 | a0001c0001t0001g0029 a0001c0006t0001g0029 |
2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.493-892T>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034914 | |||||||
| chr1:47034960 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.493-846C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47034960 | |||||||
| chr1:47035075 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0166 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.493-731C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47035075 | |||||||
| chr1:47035237 | C | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
181 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.493-569C>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47035237 | |||||||
| chr1:47035257 | CTT | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0116 others(2): Show |
10 | HG02040.hp2 NA18950.hp1 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.493-547_493-546del others(2): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 47035257 | ||||||
| chr1:47035542 | T | G | 2 | a0001c0001t0001g0029 a0001c0006t0001g0029 |
2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.493-264T>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47035542 | |||||||
| chr1:47035555 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.493-251G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47035555 | |||||||
| chr1:47035598 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.493-208C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47035598 | |||||||
| chr1:47035798 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG01261.hp1 | splice_region_variant&intron_variant | LOW | c.493-8T>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 4/11 | chr1 | 47035798 | |||||||
| chr1:47036365 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.775+194_775+195ins others(21): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036365 | |||||||
| chr1:47036368 | T | A | 1 | a0001c0001t0001g0085 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.775+197T>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036368 | |||||||
| chr1:47036368 | T | TATATATA others(14): Show |
1 | a0001c0001t0001g0054 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775+197_775+198ins others(21): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036368 | |||||||
| chr1:47036368 | T | TATATATA others(16): Show |
1 | a0001c0001t0001g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.775+197_775+198ins others(23): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036368 | |||||||
| chr1:47036368 | T | TATATATA others(18): Show |
1 | a0001c0001t0001g0055 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.775+197_775+198ins others(25): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036368 | |||||||
| chr1:47036368 | T | TATATATA others(20): Show |
1 | a0001c0001t0001g0056 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.775+197_775+198ins others(27): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036368 | |||||||
| chr1:47036368 | T | TTATATAT others(1): Show |
2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
4 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.775+198_775+199ins others(8): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(5): Show |
3 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG00558.hp1 HG01109.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.775+198_775+199ins others(12): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(7): Show |
3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0116 |
3 | HG03139.hp1 NA18970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.775+198_775+199ins others(14): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0042 |
7 | HG02818.hp1 HG04228.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.775+198_775+199ins others(16): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(11): Show |
6 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0113 others(3): Show |
12 | HG00609.hp2 HG02155.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.775+198_775+199ins others(18): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(13): Show |
7 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0090 others(4): Show |
15 | HG00140.hp1 HG01106.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.775+198_775+199ins others(20): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(15): Show |
9 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0118 others(6): Show |
10 | HG00438.hp1 HG00735.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.775+198_775+199ins others(22): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(17): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0092 |
3 | NA18612.hp1 NA18941.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.775+198_775+199ins others(24): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(19): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
5 | HG00423.hp1 HG00673.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+198_775+199ins others(26): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(21): Show |
1 | a0001c0001t0001g0037 | 2 | NA18959.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.775+198_775+199ins others(28): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036368 | T | TTATATAT others(23): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0130 a0001c0002t0004g0096 |
4 | HG03225.hp2 NA18984.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+198_775+199ins others(30): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036368 | ||||||
| chr1:47036370 | T | A | 49 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(46): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.775+199T>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036370 | |||||||
| chr1:47036370 | T | TATATATA others(14): Show |
1 | a0001c0001t0001g0058 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.775+199_775+200ins others(21): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036370 | |||||||
| chr1:47036370 | T | TTATATA | 4 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0052 others(1): Show |
12 | HG00639.hp1 HG01192.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.775+210_775+215dup others(6): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(3): Show |
1 | a0001c0001t0001g0059 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.775+206_775+215dup others(10): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(5): Show |
2 | a0001c0001t0001g0029 a0001c0006t0001g0029 |
2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.775+204_775+215dup others(12): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(7): Show |
1 | a0001c0001t0001g0009 | 7 | HG01074.hp2 HG01109.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.775+202_775+215dup others(14): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(9): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0048 others(2): Show |
19 | HG00558.hp2 HG01255.hp1 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.775+200_775+215dup others(16): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(11): Show |
5 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0046 others(2): Show |
8 | HG00639.hp2 HG01433.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(18): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(13): Show |
3 | a0001c0001t0001g0017 a0001c0001t0001g0094 a0001c0001t0001g0106 |
5 | HG02132.hp2 HG02257.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(20): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(15): Show |
4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
4 | HG02027.hp1 HG02027.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(22): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(17): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0053 others(5): Show |
13 | HG00408.hp1 HG01175.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(24): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(19): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0050 others(3): Show |
17 | HG01081.hp1 HG01943.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(26): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(21): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0072 others(11): Show |
24 | HG01070.hp2 HG01123.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(28): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(23): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0032 others(5): Show |
23 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(30): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(25): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0047 others(4): Show |
17 | HG00280.hp1 HG00408.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(32): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(27): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0082 |
3 | HG02602.hp2 HG03710.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.775+215_775+216ins others(34): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTATATAT others(31): Show |
1 | a0001c0001t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.775+215_775+216ins others(38): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTTATATA others(18): Show |
1 | a0001c0001t0001g0084 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.775+200_775+201ins others(25): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036370 | T | TTTATATA others(22): Show |
1 | a0001c0001t0001g0028 | 2 | NA19011.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.775+200_775+201ins others(29): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036370 | ||||||
| chr1:47036379 | T | TATATATA others(9): Show |
2 | a0001c0001t0001g0013 a0001c0001t0001g0044 |
7 | HG01069.hp2 HG01071.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.775+215_775+216ins others(16): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47036379 | ||||||
| chr1:47036387 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.775+216C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036387 | |||||||
| chr1:47036584 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.775+413A>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036584 | |||||||
| chr1:47036690 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.775+519G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036690 | |||||||
| chr1:47036795 | A | G | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.775+624A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036795 | |||||||
| chr1:47036811 | G | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.775+640G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036811 | |||||||
| chr1:47036812 | T | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(30): Show |
61 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.775+641T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47036812 | |||||||
| chr1:47037042 | T | C | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.775+871T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47037042 | |||||||
| chr1:47037070 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.775+899G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47037070 | |||||||
| chr1:47037272 | AT | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.775+1122delT | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47037272 | ||||||
| chr1:47037272 | ATT | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0070 a0001c0001t0001g0072 others(6): Show |
10 | HG00639.hp2 HG01070.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.775+1121_775+1122d others(4): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47037272 | ||||||
| chr1:47037422 | C | A | 1 | a0001c0001t0001g0052 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.776-1238C>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47037422 | |||||||
| chr1:47037645 | G | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02922.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.776-1015G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47037645 | |||||||
| chr1:47037648 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.776-1012G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47037648 | |||||||
| chr1:47037924 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
12 | HG00639.hp1 HG01192.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.776-736T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47037924 | |||||||
| chr1:47037971 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.776-689C>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47037971 | |||||||
| chr1:47038187 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.776-473T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47038187 | |||||||
| chr1:47038211 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.776-449G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47038211 | |||||||
| chr1:47038293 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.776-367A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47038293 | |||||||
| chr1:47038357 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.776-303G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47038357 | |||||||
| chr1:47038545 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.776-115A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 6/11 | chr1 | 47038545 | |||||||
| chr1:47038816 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.882+50A>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 7/11 | chr1 | 47038816 | |||||||
| chr1:47038863 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.882+97G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 7/11 | chr1 | 47038863 | |||||||
| chr1:47038919 | CAA | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0152 a0001c0001t0001g0153 others(3): Show |
7 | HG01891.hp2 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+155_882+156del others(2): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47038919 | ||||||
| chr1:47039045 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(30): Show |
61 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.882+279A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 7/11 | chr1 | 47039045 | |||||||
| chr1:47039054 | C | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.882+288C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 7/11 | chr1 | 47039054 | |||||||
| chr1:47039123 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.883-219T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 7/11 | chr1 | 47039123 | |||||||
| chr1:47039264 | C | A | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(30): Show |
61 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.883-78C>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 7/11 | chr1 | 47039264 | |||||||
| chr1:47039544 | A | G | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1073+12A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47039544 | |||||||
| chr1:47039605 | C | T | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1073+73C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47039605 | |||||||
| chr1:47039710 | GA | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
181 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1073+191delA | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47039710 | ||||||
| chr1:47039710 | GAA | G | 38 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(35): Show |
66 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.1073+190_1073+191d others(4): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47039710 | ||||||
| chr1:47039724 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1073+192G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47039724 | |||||||
| chr1:47039945 | C | T | 2 | a0001c0002t0004g0095 a0001c0002t0004g0096 |
2 | HG02486.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1073+413C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47039945 | |||||||
| chr1:47040015 | TAGTTA | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1073+488_1073+492d others(7): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47040015 | ||||||
| chr1:47040173 | G | T | 1 | a0001c0001t0002g0031 | 2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1073+641G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040173 | |||||||
| chr1:47040231 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1073+699G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040231 | |||||||
| chr1:47040264 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0166 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1073+732T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040264 | |||||||
| chr1:47040269 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1073+737G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040269 | |||||||
| chr1:47040451 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1073+919G>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040451 | |||||||
| chr1:47040680 | T | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(74): Show |
156 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1073+1148T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040680 | |||||||
| chr1:47040685 | ATG | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1073+1159_1073+116 others(6): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47040685 | ||||||
| chr1:47040766 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1073+1234A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040766 | |||||||
| chr1:47040767 | T | C | 42 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(39): Show |
72 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1073+1235T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040767 | |||||||
| chr1:47040833 | T | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(30): Show |
61 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1073+1301T>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040833 | |||||||
| chr1:47040854 | G | T | 32 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(29): Show |
59 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1073+1322G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47040854 | |||||||
| chr1:47041087 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1073+1555A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47041087 | |||||||
| chr1:47041132 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1073+1600A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47041132 | |||||||
| chr1:47041169 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1073+1637T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47041169 | |||||||
| chr1:47041367 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1073+1835G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47041367 | |||||||
| chr1:47041475 | C | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1073+1943C>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47041475 | |||||||
| chr1:47041545 | A | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1073+2013A>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47041545 | |||||||
| chr1:47042020 | A | G | 36 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(33): Show |
64 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1073+2488A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042020 | |||||||
| chr1:47042114 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1073+2582T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042114 | |||||||
| chr1:47042136 | T | C | 34 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(31): Show |
62 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1073+2604T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042136 | |||||||
| chr1:47042267 | T | G | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1073+2735T>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042267 | |||||||
| chr1:47042286 | CT | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
153 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1073+2767delT | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47042286 | ||||||
| chr1:47042286 | CTT | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(49): Show |
97 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1073+2766_1073+276 others(6): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47042286 | ||||||
| chr1:47042301 | G | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1073+2769G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042301 | |||||||
| chr1:47042488 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1073+2956G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042488 | |||||||
| chr1:47042683 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1073+3151C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042683 | |||||||
| chr1:47042704 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1073+3172T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042704 | |||||||
| chr1:47042775 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1073+3243G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042775 | |||||||
| chr1:47042803 | G | T | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1073+3271G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042803 | |||||||
| chr1:47042825 | A | G | 36 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(33): Show |
64 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.1073+3293A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042825 | |||||||
| chr1:47042885 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1073+3353C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47042885 | |||||||
| chr1:47043082 | G | A | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1074-3385G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043082 | |||||||
| chr1:47043281 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1074-3186C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043281 | |||||||
| chr1:47043656 | T | G | 2 | a0001c0001t0001g0029 a0001c0006t0001g0029 |
2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1074-2811T>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043656 | |||||||
| chr1:47043684 | G | T | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1074-2783G>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043684 | |||||||
| chr1:47043722 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1074-2745T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043722 | |||||||
| chr1:47043754 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0001g0165 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1074-2713C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043754 | |||||||
| chr1:47043836 | A | C | 1 | a0001c0001t0001g0075 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1074-2631A>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043836 | |||||||
| chr1:47043841 | A | G | 43 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
73 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1074-2626A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043841 | |||||||
| chr1:47043897 | T | C | 2 | a0001c0001t0001g0100 a0003c0007t0001g0099 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1074-2570T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043897 | |||||||
| chr1:47043900 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1074-2567A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043900 | |||||||
| chr1:47043940 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0166 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074-2527T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043940 | |||||||
| chr1:47043964 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074-2503G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47043964 | |||||||
| chr1:47044215 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1074-2252T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47044215 | |||||||
| chr1:47044316 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1074-2151A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47044316 | |||||||
| chr1:47044494 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1074-1973G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47044494 | |||||||
| chr1:47044537 | CACT | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(62): Show |
135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1074-1927_1074-192 others(7): Show |
CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47044537 | ||||||
| chr1:47044679 | T | C | 6 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0032 others(3): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1074-1788T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47044679 | |||||||
| chr1:47044751 | C | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0079 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1074-1716C>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47044751 | |||||||
| chr1:47044787 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1074-1680T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47044787 | |||||||
| chr1:47044824 | C | CT | 35 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(32): Show |
63 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1074-1630dupT | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47044824 | ||||||
| chr1:47044928 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(81): Show |
171 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1074-1539G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47044928 | |||||||
| chr1:47045230 | A | G | 33 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(30): Show |
61 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.1074-1237A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47045230 | |||||||
| chr1:47045641 | G | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1074-826G>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47045641 | |||||||
| chr1:47045846 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02922.hp1 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1074-621A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47045846 | |||||||
| chr1:47046012 | T | C | 1 | a0005c0008t0001g0167 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1074-455T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 8/11 | chr1 | 47046012 | |||||||
| chr1:47046638 | A | G | 1 | a0001c0001t0001g0040 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1207+38A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47046638 | |||||||
| chr1:47046871 | T | C | 1 | a0001c0001t0001g0014 | 5 | HG01257.hp2 HG01258.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207+271T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47046871 | |||||||
| chr1:47047089 | C | T | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1207+489C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047089 | |||||||
| chr1:47047151 | C | T | 3 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0001g0165 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1207+551C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047151 | |||||||
| chr1:47047217 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1207+617C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047217 | |||||||
| chr1:47047315 | A | G | 2 | a0001c0001t0003g0163 a0001c0001t0003g0164 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1207+715A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047315 | |||||||
| chr1:47047411 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0166 others(5): Show |
10 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207+811A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047411 | |||||||
| chr1:47047686 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1208-879C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047686 | |||||||
| chr1:47047862 | G | A | 3 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0045 |
5 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1208-703G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047862 | |||||||
| chr1:47047913 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1208-652A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047913 | |||||||
| chr1:47047914 | C | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0013 others(31): Show |
62 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1208-651C>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047914 | |||||||
| chr1:47047980 | C | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(35): Show |
73 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1208-585C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47047980 | |||||||
| chr1:47048079 | CA | C | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
231 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1208-473delA | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47048079 | ||||||
| chr1:47048352 | A | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1208-213A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 9/11 | chr1 | 47048352 | |||||||
| chr1:47048736 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1272+107A>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47048736 | |||||||
| chr1:47048875 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
12 | HG00639.hp1 HG01192.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1272+246A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47048875 | |||||||
| chr1:47049060 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1273-362A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47049060 | |||||||
| chr1:47049081 | G | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0134 a0001c0001t0001g0141 others(5): Show |
9 | HG02280.hp2 HG02723.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1273-341G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47049081 | |||||||
| chr1:47049120 | T | C | 1 | a0001c0001t0001g0014 | 5 | HG01257.hp2 HG01258.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-302T>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47049120 | |||||||
| chr1:47049140 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1273-282A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47049140 | |||||||
| chr1:47049347 | C | T | 1 | a0003c0007t0001g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1273-75C>T | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47049347 | |||||||
| chr1:47049358 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0166 others(3): Show |
8 | HG02055.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1273-64G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47049358 | |||||||
| chr1:47049416 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp2 | splice_region_variant&intron_variant | LOW | c.1273-6T>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 10/11 | chr1 | 47049416 | |||||||
| chr1:47049551 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1355+47G>A | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 11/11 | chr1 | 47049551 | |||||||
| chr1:47049660 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
20 | HG00639.hp1 HG00673.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.1355+156A>G | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 11/11 | chr1 | 47049660 | |||||||
| chr1:47049891 | G | GA | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1356-104dupA | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 47049891 | ||||||
| chr1:47049924 | A | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(124): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.1356-76A>C | CYP4X1 | ENSG00000186377.8 | transcript | ENST00000371901.4 | protein_coding | 11/11 | chr1 | 47049924 |