Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 199974 |
| ensemblid | ENSG00000186160.5 |
| hgncid | 20583 |
| symbol | CYP4Z1 |
| name | cytochrome P450 family 4 subfamily Z member 1 |
| refseq_nuc | NM_178134.3 |
| refseq_prot | NP_835235.1 |
| ensembl_nuc | ENST00000334194.4 |
| ensembl_prot | ENSP00000334246.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 47067231 |
| end | 47118318 |
| strand | + |
| ver | v1.2 |
| region | chr1:47067231-47118318 |
| region5000 | chr1:47062231-47123318 |
| regionname0 | CYP4Z1_chr1_47067231_47118318 |
| regionname5000 | CYP4Z1_chr1_47062231_47123318 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 505 | 309 | 84 | 70 | 112 | 11 | 30 | 84 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | MEPSW others(500): Show |
chr1 | 47062231 | 47123318 |
| a0002 | 0/0 | 505 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | MEPSW others(500): Show |
chr1 | 47062231 | 47123318 |
| a0003 | 0/0 | 505 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | MEPSW others(500): Show |
chr1 | 47062231 | 47123318 |
| a0004 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | MEPSW others(500): Show |
chr1 | 47062231 | 47123318 |
| a0005 | 0/0 | 505 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | MEPSW others(500): Show |
chr1 | 47062231 | 47123318 |
| a0006 | 0/0 | 505 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | MEPSW others(500): Show |
chr1 | 47062231 | 47123318 |
| a0007 | 0/0 | 505 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | MEPSW others(500): Show |
chr1 | 47062231 | 47123318 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1515 | 211 | 41 | 36 | 109 | 6 | 18 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0001c0002 | 1/0 | 1515 | 94 | 40 | 34 | 3 | 5 | 11 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0001c0005 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0001c0008 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0001c0010 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0002c0003 | 0/0 | 1515 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0003c0004 | 0/0 | 1515 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0004c0011 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0005c0007 | 0/0 | 1515 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0006c0006 | 0/0 | 1515 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 | ||
| a0007c0009 | 0/0 | 1515 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATGGA others(1510): Show |
chr1 | 47062231 | 47123318 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2162 | 208 | 39 | 36 | 108 | 6 | 18 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0001c0001t0002 | 0/0 | 2162 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0001c0001t0003 | 0/0 | 2162 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0001c0002t0001 | 1/0 | 2162 | 94 | 40 | 34 | 3 | 5 | 11 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0001c0005t0001 | 0/0 | 2162 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0001c0008t0001 | 0/0 | 2162 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0001c0010t0001 | 0/0 | 2162 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0002c0003t0001 | 0/0 | 2162 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0003c0004t0001 | 0/0 | 2162 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0004c0011t0001 | 0/0 | 2162 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0005c0007t0001 | 0/0 | 2162 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0006c0006t0001 | 0/0 | 2162 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| a0007c0009t0001 | 0/0 | 2162 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | ATATG others(2157): Show |
chr1 | 47062231 | 47123318 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 11 | 0 | 0 | 7 | 1 | 3 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0002 | 0/0 | 9 | 1 | 0 | 8 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0041 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0003 | 0/0 | 8 | 0 | 2 | 1 | 3 | 2 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0057 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0005t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0008t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0001c0010t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0002c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0002c0003t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0003c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0003c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0004c0011t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0005c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0006c0006t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| a0007c0009t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | GBR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0011 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0003 | EUR | IBS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0010 | EUR | IBS | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CDX | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02258 | hp2 | a0001 | c0008 | t0001 | g0091 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | KHV | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02572 | hp1 | a0004 | c0011 | t0001 | g0085 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02896 | hp1 | a0003 | c0004 | t0001 | g0095 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02897 | hp1 | a0003 | c0004 | t0001 | g0094 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0052 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02976 | hp2 | a0001 | c0005 | t0001 | g0021 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0021 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03209 | hp1 | a0005 | c0007 | t0001 | g0115 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0007 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | ESN | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0066 | AFR | GWD | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03669 | hp2 | a0001 | c0010 | t0001 | g0121 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | BEB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | BEB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0087 | SAS | STU | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0086 | SAS | STU | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0063 | SAS | STU | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | YRI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18975 | hp1 | a0006 | c0006 | t0001 | g0162 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18984 | hp2 | a0002 | c0003 | t0001 | g0195 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19003 | hp2 | a0002 | c0003 | t0001 | g0196 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | LWK | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | LWK | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | YRI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ASW | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0062 | AFR | ASW | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | TSI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA20752 | hp2 | a0007 | c0009 | t0001 | g0133 | EUR | TSI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0081 | EUR | TSI | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | MSL | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | LWK | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0170 | REF | REF | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0057 | REF | REF | CYP4Z1_chr1_47062231_47123318 | CYP4Z1 | chr1 | 47062231 | 47123318 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47067617 | C | A | 1 | a0006 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.127C>A | p.Leu43Met | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/12 | 387/2162 | 127/1518 | 43/505 | chr1 | 47067617 | |||
| chr1:47067638 | C | T | 1 | a0004 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.148C>T | p.Pro50Ser | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/12 | 408/2162 | 148/1518 | 50/505 | chr1 | 47067638 | |||
| chr1:47082432 | A | G | 1 | a0002 | 3 | NA18984.hp2 NA18989.hp1 NA19003.hp2 |
missense_variant | MODERATE | c.463A>G | p.Met155Val | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/12 | 723/2162 | 463/1518 | 155/505 | chr1 | 47082432 | |||
| chr1:47084654 | G | A | 1 | a0003 | 2 | HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.527G>A | p.Arg176His | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 5/12 | 787/2162 | 527/1518 | 176/505 | chr1 | 47084654 | |||
| chr1:47094637 | T | C | 1 | a0005 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.844T>C | p.Trp282Arg | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/12 | 1104/2162 | 844/1518 | 282/505 | chr1 | 47094637 | |||
| chr1:47094638 | G | A | 1 | a0005 | 1 | HG03209.hp1 | stop_gained | HIGH | c.845G>A | p.Trp282* | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/12 | 1105/2162 | 845/1518 | 282/505 | chr1 | 47094638 | |||
| chr1:47106190 | C | G | 1 | a0007 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1130C>G | p.Ala377Gly | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/12 | 1390/2162 | 1130/1518 | 377/505 | chr1 | 47106190 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47094633 | G | A | 1 | a0005c0007 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.840G>A | p.Arg280Arg | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/12 | 1100/2162 | 840/1518 | 280/505 | chr1 | 47094633 | |||
| chr1:47106158 | G | A | 1 | a0001c0008 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.1098G>A | p.Thr366Thr | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/12 | 1358/2162 | 1098/1518 | 366/505 | chr1 | 47106158 | |||
| chr1:47106188 | C | T | 1 | a0001c0010 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1128C>T | p.Tyr376Tyr | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/12 | 1388/2162 | 1128/1518 | 376/505 | chr1 | 47106188 | |||
| chr1:47106230 | C | T | 7 | a0001c0001 a0001c0005 a0001c0010 others(4): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
synonymous_variant | LOW | c.1170C>T | p.Ile390Ile | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/12 | 1430/2162 | 1170/1518 | 390/505 | chr1 | 47106230 | |||
| chr1:47106233 | C | T | 6 | a0001c0001 a0001c0010 a0002c0003 others(3): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
synonymous_variant | LOW | c.1173C>T | p.Thr391Thr | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/12 | 1433/2162 | 1173/1518 | 391/505 | chr1 | 47106233 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47067361 | C | G | 1 | a0001c0001t0003 | 1 | HG00558.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/12 | 130 | chr1 | 47067361 | ||||||
| chr1:47117951 | A | G | 1 | a0001c0001t0002 | 2 | HG03139.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*17A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 12/12 | 17 | chr1 | 47117951 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:47067701 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.177+34G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/11 | chr1 | 47067701 | |||||||
| chr1:47067760 | G | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0221 |
5 | HG01069.hp1 HG01071.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+93G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/11 | chr1 | 47067760 | |||||||
| chr1:47067825 | A | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG01243.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.177+158A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/11 | chr1 | 47067825 | |||||||
| chr1:47068165 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.178-457G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/11 | chr1 | 47068165 | |||||||
| chr1:47068435 | A | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.178-187A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/11 | chr1 | 47068435 | |||||||
| chr1:47068587 | C | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-35C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 1/11 | chr1 | 47068587 | |||||||
| chr1:47068778 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.319+15G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47068778 | |||||||
| chr1:47068792 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.319+29G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47068792 | |||||||
| chr1:47068834 | G | A | 8 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(5): Show |
11 | HG00639.hp1 HG01192.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.319+71G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47068834 | |||||||
| chr1:47068964 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.319+201T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47068964 | |||||||
| chr1:47069282 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.319+519C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069282 | |||||||
| chr1:47069441 | GCC | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.319+679_319+680del others(2): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069441 | |||||||
| chr1:47069463 | A | G | 1 | a0001c0002t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.319+700A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069463 | |||||||
| chr1:47069507 | T | C | 1 | a0001c0002t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.319+744T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069507 | |||||||
| chr1:47069608 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.319+845A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069608 | |||||||
| chr1:47069687 | A | G | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0209 others(3): Show |
6 | HG02300.hp1 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+924A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069687 | |||||||
| chr1:47069694 | G | C | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0209 others(3): Show |
6 | HG02300.hp1 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+931G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069694 | |||||||
| chr1:47069703 | C | T | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0209 others(3): Show |
6 | HG02300.hp1 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+940C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069703 | |||||||
| chr1:47069871 | C | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.319+1108C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069871 | |||||||
| chr1:47069973 | A | G | 1 | a0001c0002t0001g0029 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.319+1210A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47069973 | |||||||
| chr1:47070085 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
225 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.319+1322G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070085 | |||||||
| chr1:47070122 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.319+1359T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070122 | |||||||
| chr1:47070306 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.319+1543A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070306 | |||||||
| chr1:47070324 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.319+1561T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070324 | |||||||
| chr1:47070345 | A | G | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.319+1582A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070345 | |||||||
| chr1:47070389 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.319+1626C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070389 | |||||||
| chr1:47070435 | G | GTACACAT | 15 | a0001c0001t0001g0096 a0001c0002t0001g0007 a0001c0002t0001g0049 others(12): Show |
20 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.319+1675_319+1681d others(9): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47070435 | ||||||
| chr1:47070473 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.319+1710C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070473 | |||||||
| chr1:47070538 | T | A | 1 | a0001c0002t0001g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.319+1775T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070538 | |||||||
| chr1:47070615 | T | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.319+1852T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070615 | |||||||
| chr1:47070838 | A | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
10 | HG01261.hp1 HG01496.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.319+2075A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070838 | |||||||
| chr1:47070875 | C | G | 1 | a0001c0002t0001g0089 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.319+2112C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47070875 | |||||||
| chr1:47071570 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(40): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.319+2807T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47071570 | |||||||
| chr1:47071836 | A | G | 2 | a0001c0002t0001g0011 a0001c0002t0001g0088 |
4 | HG01081.hp2 HG01106.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+3073A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47071836 | |||||||
| chr1:47071982 | T | TGATAGAT others(5): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0103 |
3 | HG02257.hp2 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.319+3233_319+3244d others(14): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47071982 | ||||||
| chr1:47071982 | T | TGATAGAT others(9): Show |
4 | a0001c0001t0001g0030 a0001c0001t0001g0100 a0001c0001t0001g0101 others(1): Show |
5 | HG02055.hp1 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+3229_319+3244d others(18): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47071982 | ||||||
| chr1:47071982 | TGATA | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(134): Show |
202 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.319+3241_319+3244d others(6): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47071982 | ||||||
| chr1:47072004 | A | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0209 a0001c0001t0002g0207 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.319+3241A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072004 | |||||||
| chr1:47072062 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.319+3299A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072062 | |||||||
| chr1:47072068 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.319+3305A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072068 | |||||||
| chr1:47072141 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(192): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.319+3378C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072141 | |||||||
| chr1:47072178 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.319+3415C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072178 | |||||||
| chr1:47072368 | A | C | 53 | a0001c0001t0001g0042 a0001c0001t0001g0084 a0001c0001t0001g0173 others(50): Show |
81 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.319+3605A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072368 | |||||||
| chr1:47072484 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.319+3721T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072484 | |||||||
| chr1:47072540 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.319+3777G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072540 | |||||||
| chr1:47072568 | C | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(6): Show |
12 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.319+3805C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072568 | |||||||
| chr1:47072678 | T | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.319+3915T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072678 | |||||||
| chr1:47072679 | G | A | 2 | a0001c0001t0001g0114 a0001c0002t0001g0090 |
2 | HG03041.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.319+3916G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072679 | |||||||
| chr1:47072784 | G | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.319+4021G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072784 | |||||||
| chr1:47072799 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.319+4036T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072799 | |||||||
| chr1:47072833 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.319+4070G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072833 | |||||||
| chr1:47072848 | T | G | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(198): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.319+4085T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072848 | |||||||
| chr1:47072883 | A | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+4120A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072883 | |||||||
| chr1:47072899 | C | T | 14 | a0001c0001t0001g0018 a0001c0001t0001g0191 a0001c0001t0001g0194 others(11): Show |
16 | HG00423.hp1 HG00438.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.319+4136C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072899 | |||||||
| chr1:47072918 | T | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0114 a0001c0002t0001g0090 |
3 | HG03041.hp2 HG03490.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.319+4155T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072918 | |||||||
| chr1:47072935 | G | A | 3 | a0001c0001t0001g0114 a0001c0002t0001g0007 a0001c0002t0001g0090 |
7 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+4172G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072935 | |||||||
| chr1:47072966 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.319+4203G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47072966 | |||||||
| chr1:47073052 | G | C | 1 | a0001c0001t0001g0218 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.319+4289G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073052 | |||||||
| chr1:47073073 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.319+4310C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073073 | |||||||
| chr1:47073074 | A | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(201): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.319+4311A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073074 | |||||||
| chr1:47073317 | G | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.319+4554G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073317 | |||||||
| chr1:47073463 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0220 |
4 | HG01243.hp1 HG02572.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4700A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073463 | |||||||
| chr1:47073544 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0189 a0001c0001t0001g0190 |
4 | NA18970.hp2 NA18980.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+4781C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073544 | |||||||
| chr1:47073588 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.319+4825C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073588 | |||||||
| chr1:47073631 | C | T | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(91): Show |
143 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.319+4868C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073631 | |||||||
| chr1:47073636 | C | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(200): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.319+4873C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073636 | |||||||
| chr1:47073647 | C | A | 1 | a0001c0005t0001g0021 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.319+4884C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073647 | |||||||
| chr1:47073741 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.319+4978A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073741 | |||||||
| chr1:47073781 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.319+5018G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073781 | |||||||
| chr1:47073868 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.319+5105T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073868 | |||||||
| chr1:47073868 | T | G | 5 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0008t0001g0091 others(2): Show |
5 | HG02258.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+5105T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47073868 | |||||||
| chr1:47074125 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.319+5362A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074125 | |||||||
| chr1:47074204 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.319+5441A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074204 | |||||||
| chr1:47074446 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.319+5683T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074446 | |||||||
| chr1:47074489 | GT | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0174 a0001c0002t0001g0029 |
5 | HG02132.hp1 HG02523.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+5733delT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47074489 | ||||||
| chr1:47074546 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.319+5783G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074546 | |||||||
| chr1:47074580 | T | C | 1 | a0001c0002t0001g0059 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.319+5817T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074580 | |||||||
| chr1:47074680 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(6): Show |
12 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.319+5917G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074680 | |||||||
| chr1:47074748 | G | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0219 |
2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.320-5875G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074748 | |||||||
| chr1:47074876 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.320-5747C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074876 | |||||||
| chr1:47074959 | A | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0174 a0001c0002t0001g0029 |
5 | HG02132.hp1 HG02523.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-5664A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074959 | |||||||
| chr1:47074977 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.320-5646A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47074977 | |||||||
| chr1:47075043 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.320-5580C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075043 | |||||||
| chr1:47075189 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
5 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-5434G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075189 | |||||||
| chr1:47075220 | T | C | 1 | a0001c0001t0001g0045 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.320-5403T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075220 | |||||||
| chr1:47075385 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-5238C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075385 | |||||||
| chr1:47075388 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.320-5235A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075388 | |||||||
| chr1:47075405 | G | A | 3 | a0001c0002t0001g0006 a0001c0002t0001g0060 a0001c0002t0001g0061 |
7 | HG01074.hp2 HG01928.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.320-5218G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075405 | |||||||
| chr1:47075614 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.320-5009C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075614 | |||||||
| chr1:47075643 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
10 | HG00609.hp2 HG02071.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.320-4980A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075643 | |||||||
| chr1:47075726 | G | T | 2 | a0003c0004t0001g0094 a0003c0004t0001g0095 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.320-4897G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075726 | |||||||
| chr1:47075733 | A | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
210 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.320-4890A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075733 | |||||||
| chr1:47075770 | G | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(40): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.320-4853G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075770 | |||||||
| chr1:47075809 | C | A | 1 | a0001c0002t0001g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.320-4814C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075809 | |||||||
| chr1:47075814 | C | T | 1 | a0001c0002t0001g0054 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.320-4809C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075814 | |||||||
| chr1:47075859 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
208 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.320-4764C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47075859 | |||||||
| chr1:47076056 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.320-4567T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076056 | |||||||
| chr1:47076273 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0174 a0001c0002t0001g0063 |
4 | HG02132.hp1 HG02523.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-4350C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076273 | |||||||
| chr1:47076512 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.320-4111T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076512 | |||||||
| chr1:47076518 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.320-4105T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076518 | |||||||
| chr1:47076542 | G | C | 1 | a0001c0002t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.320-4081G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076542 | |||||||
| chr1:47076549 | TAAGAATG others(304): Show |
T | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-4059_320-3749d others(2): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076549 | ||||||
| chr1:47076557 | T | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-4066T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076557 | |||||||
| chr1:47076584 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0130 |
2 | HG02602.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.320-4039G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076584 | |||||||
| chr1:47076646 | C | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.320-3977C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076646 | |||||||
| chr1:47076661 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.320-3962C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076661 | |||||||
| chr1:47076708 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.320-3915G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076708 | |||||||
| chr1:47076754 | A | C | 1 | a0001c0002t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.320-3869A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076754 | |||||||
| chr1:47076762 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.320-3861G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076762 | |||||||
| chr1:47076780 | C | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.320-3843C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076780 | |||||||
| chr1:47076823 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.320-3800C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076823 | |||||||
| chr1:47076826 | C | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.320-3797C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076826 | |||||||
| chr1:47076837 | G | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0209 a0001c0001t0002g0207 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-3786G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076837 | |||||||
| chr1:47076844 | C | CAA | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(31): Show |
52 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.320-3762_320-3761d others(4): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAA | 13 | a0001c0001t0001g0012 a0001c0001t0001g0043 a0001c0001t0001g0105 others(10): Show |
15 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-3763_320-3761d others(5): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAA | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(2): Show |
7 | HG02257.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-3765_320-3761d others(7): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
15 | HG00280.hp2 HG00408.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-3766_320-3761d others(8): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0134 |
2 | HG01361.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.320-3771_320-3761d others(13): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0169 |
3 | NA18941.hp2 NA18952.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.320-3774_320-3761d others(16): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0015 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.320-3775_320-3761d others(17): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.320-3778_320-3761d others(20): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(16): Show |
18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(15): Show |
21 | HG01070.hp1 HG01074.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.320-3761_320-3760i others(25): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(17): Show |
23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0034 others(20): Show |
27 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.320-3761_320-3760i others(26): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(18): Show |
20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(17): Show |
25 | HG00558.hp2 HG01175.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.320-3761_320-3760i others(27): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(19): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0035 others(8): Show |
12 | HG00738.hp1 HG01496.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-3761_320-3760i others(28): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(20): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0039 others(4): Show |
8 | HG00408.hp1 HG02647.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.320-3761_320-3760i others(29): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(21): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0036 others(3): Show |
7 | HG01517.hp1 HG01952.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.320-3761_320-3760i others(30): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(22): Show |
4 | a0001c0001t0001g0036 a0001c0001t0001g0160 a0001c0001t0001g0171 others(1): Show |
4 | HG00423.hp2 HG01109.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-3761_320-3760i others(31): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(25): Show |
1 | a0001c0001t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320-3761_320-3760i others(34): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(41): Show |
1 | a0001c0001t0001g0135 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.320-3761_320-3760i others(50): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | C | CAAAAAAA others(46): Show |
1 | a0001c0001t0001g0161 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.320-3761_320-3760i others(55): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076844 | CA | C | 69 | a0001c0001t0001g0055 a0001c0001t0001g0084 a0001c0001t0001g0112 others(66): Show |
101 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(98): Show |
intron_variant | MODIFIER | c.320-3761delA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47076844 | ||||||
| chr1:47076901 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02132.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.320-3722C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076901 | |||||||
| chr1:47076902 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.320-3721G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076902 | |||||||
| chr1:47076987 | T | C | 2 | a0001c0001t0001g0210 a0001c0002t0001g0063 |
2 | HG04204.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.320-3636T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47076987 | |||||||
| chr1:47077120 | C | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(40): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.320-3503C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077120 | |||||||
| chr1:47077174 | TG | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(6): Show |
12 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-3448delG | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077174 | |||||||
| chr1:47077193 | A | G | 1 | a0001c0002t0001g0007 | 5 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-3430A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077193 | |||||||
| chr1:47077197 | T | G | 1 | a0001c0010t0001g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.320-3426T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077197 | |||||||
| chr1:47077225 | T | A | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-3398T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077225 | |||||||
| chr1:47077361 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-3262G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077361 | |||||||
| chr1:47077364 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0169 |
4 | NA18941.hp2 NA18952.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-3259A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077364 | |||||||
| chr1:47077367 | G | C | 1 | a0001c0002t0001g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.320-3256G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077367 | |||||||
| chr1:47077495 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-3128G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077495 | |||||||
| chr1:47077509 | C | G | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-3114C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077509 | |||||||
| chr1:47077625 | A | AT | 4 | a0001c0001t0001g0004 a0001c0001t0001g0187 a0001c0001t0001g0188 others(1): Show |
10 | HG00609.hp2 HG01993.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.320-2986dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47077625 | ||||||
| chr1:47077625 | A | T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0209 a0001c0001t0002g0207 others(2): Show |
5 | HG02559.hp1 HG02922.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-2998A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077625 | |||||||
| chr1:47077657 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2966G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077657 | |||||||
| chr1:47077674 | G | C | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2949G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077674 | |||||||
| chr1:47077711 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2912C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077711 | |||||||
| chr1:47077755 | G | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(39): Show |
61 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.320-2868G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077755 | |||||||
| chr1:47077761 | C | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.320-2862C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077761 | |||||||
| chr1:47077771 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.320-2852C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077771 | |||||||
| chr1:47077844 | G | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.320-2779G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077844 | |||||||
| chr1:47077853 | A | G | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2770A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077853 | |||||||
| chr1:47077858 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2765G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077858 | |||||||
| chr1:47077882 | A | G | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2741A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47077882 | |||||||
| chr1:47078066 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.320-2557C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078066 | |||||||
| chr1:47078067 | G | A | 2 | a0001c0001t0001g0122 a0001c0002t0001g0063 |
2 | HG01943.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.320-2556G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078067 | |||||||
| chr1:47078070 | A | G | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2553A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078070 | |||||||
| chr1:47078085 | T | C | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2538T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078085 | |||||||
| chr1:47078092 | G | C | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2531G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078092 | |||||||
| chr1:47078097 | T | G | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2526T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078097 | |||||||
| chr1:47078107 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2516C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078107 | |||||||
| chr1:47078135 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2488C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078135 | |||||||
| chr1:47078213 | T | C | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2410T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078213 | |||||||
| chr1:47078215 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2408C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078215 | |||||||
| chr1:47078231 | T | C | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2392T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078231 | |||||||
| chr1:47078242 | C | T | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2381C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078242 | |||||||
| chr1:47078255 | C | G | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2368C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078255 | |||||||
| chr1:47078272 | T | A | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.320-2351T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078272 | |||||||
| chr1:47078327 | T | G | 3 | a0001c0001t0001g0105 a0001c0002t0001g0063 a0001c0002t0001g0066 |
3 | HG02451.hp1 HG03540.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.320-2296T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078327 | |||||||
| chr1:47078754 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.320-1869T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078754 | |||||||
| chr1:47078755 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(76): Show |
114 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.320-1868G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078755 | |||||||
| chr1:47078807 | A | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | NA18980.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.320-1816A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078807 | |||||||
| chr1:47078809 | G | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0185 |
4 | NA18950.hp2 NA18960.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-1814G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078809 | |||||||
| chr1:47078872 | G | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0173 |
2 | HG00609.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.320-1751G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078872 | |||||||
| chr1:47078894 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0185 |
4 | NA18950.hp2 NA18960.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-1729T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078894 | |||||||
| chr1:47078959 | T | A | 1 | a0001c0002t0001g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.320-1664T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47078959 | |||||||
| chr1:47079185 | A | T | 3 | a0001c0002t0001g0058 a0001c0002t0001g0090 a0001c0002t0001g0097 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.320-1438A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079185 | |||||||
| chr1:47079231 | G | A | 1 | a0001c0002t0001g0007 | 5 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-1392G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079231 | |||||||
| chr1:47079242 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.320-1381G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079242 | |||||||
| chr1:47079270 | C | A | 16 | a0001c0001t0001g0055 a0001c0002t0001g0007 a0001c0002t0001g0049 others(13): Show |
21 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.320-1353C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079270 | |||||||
| chr1:47079287 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.320-1336C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079287 | |||||||
| chr1:47079300 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.320-1323T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079300 | |||||||
| chr1:47079371 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.320-1252G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079371 | |||||||
| chr1:47079453 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.320-1170C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079453 | |||||||
| chr1:47079640 | G | A | 36 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0008 others(33): Show |
57 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.320-983G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079640 | |||||||
| chr1:47079755 | G | A | 3 | a0001c0002t0001g0022 a0001c0002t0001g0065 a0001c0002t0001g0071 |
4 | HG00735.hp1 HG01169.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-868G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079755 | |||||||
| chr1:47079769 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.320-854G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079769 | |||||||
| chr1:47079849 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.320-774T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079849 | |||||||
| chr1:47079868 | GGA | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.320-734_320-733del others(2): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47079868 | ||||||
| chr1:47079875 | G | A | 1 | a0001c0002t0001g0088 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.320-748G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47079875 | |||||||
| chr1:47080040 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.320-583C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47080040 | |||||||
| chr1:47080070 | C | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0166 |
4 | NA18939.hp2 NA18982.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-553C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47080070 | |||||||
| chr1:47080136 | A | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.320-487A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47080136 | |||||||
| chr1:47080249 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.320-374G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47080249 | |||||||
| chr1:47080250 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(90): Show |
132 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.320-373T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47080250 | |||||||
| chr1:47080314 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.320-309A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47080314 | |||||||
| chr1:47080362 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.320-261T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47080362 | |||||||
| chr1:47080534 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.320-89G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | chr1 | 47080534 | |||||||
| chr1:47080610 | TTC | T | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(6): Show |
12 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.320-11_320-10delCT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 47080610 | ||||||
| chr1:47080814 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.364+147G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47080814 | |||||||
| chr1:47080942 | C | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0209 a0001c0001t0002g0207 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.364+275C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47080942 | |||||||
| chr1:47081200 | T | C | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.364+533T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47081200 | |||||||
| chr1:47081589 | G | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.365-745G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47081589 | |||||||
| chr1:47081622 | A | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.365-712A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47081622 | |||||||
| chr1:47081766 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.365-568C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47081766 | |||||||
| chr1:47081767 | C | T | 6 | a0001c0002t0001g0059 a0001c0002t0001g0067 a0001c0002t0001g0068 others(3): Show |
6 | HG00738.hp2 HG01175.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.365-567C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47081767 | |||||||
| chr1:47081937 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.365-397C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47081937 | |||||||
| chr1:47081959 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.365-375C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47081959 | |||||||
| chr1:47081976 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.365-358C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47081976 | |||||||
| chr1:47082001 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(6): Show |
12 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.365-333G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47082001 | |||||||
| chr1:47082018 | C | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.365-316C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47082018 | |||||||
| chr1:47082134 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.365-200A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47082134 | |||||||
| chr1:47082300 | C | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.365-34C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 3/11 | chr1 | 47082300 | |||||||
| chr1:47082537 | A | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0201 a0001c0001t0001g0202 |
5 | NA18612.hp2 NA18939.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.492+76A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47082537 | |||||||
| chr1:47082636 | A | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.492+175A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47082636 | |||||||
| chr1:47082718 | A | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.492+257A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47082718 | |||||||
| chr1:47082840 | C | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.492+379C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47082840 | |||||||
| chr1:47083030 | T | C | 1 | a0001c0002t0001g0049 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.492+569T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083030 | |||||||
| chr1:47083049 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(40): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.492+588G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083049 | |||||||
| chr1:47083077 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.492+616G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083077 | |||||||
| chr1:47083302 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(76): Show |
114 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.492+841G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083302 | |||||||
| chr1:47083360 | T | C | 1 | a0001c0002t0001g0073 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.492+899T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083360 | |||||||
| chr1:47083586 | A | T | 4 | a0001c0001t0001g0096 a0001c0001t0001g0209 a0001c0001t0002g0207 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.493-1034A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083586 | |||||||
| chr1:47083645 | A | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.493-975A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083645 | |||||||
| chr1:47083847 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.493-773A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083847 | |||||||
| chr1:47083848 | T | A | 1 | a0001c0002t0001g0087 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.493-772T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083848 | |||||||
| chr1:47083969 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.493-651G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47083969 | |||||||
| chr1:47084088 | G | T | 1 | a0001c0002t0001g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.493-532G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47084088 | |||||||
| chr1:47084337 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0211 a0001c0001t0001g0212 |
5 | NA18979.hp1 NA18982.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.493-283T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47084337 | |||||||
| chr1:47084430 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.493-190G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47084430 | |||||||
| chr1:47084473 | C | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.493-147C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47084473 | |||||||
| chr1:47084493 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.493-127A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47084493 | |||||||
| chr1:47084502 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.493-118A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47084502 | |||||||
| chr1:47084508 | T | G | 9 | a0001c0001t0001g0084 a0001c0002t0001g0009 a0001c0002t0001g0026 others(6): Show |
13 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.493-112T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47084508 | |||||||
| chr1:47084574 | G | GA | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.493-43dupA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 47084574 | ||||||
| chr1:47084600 | A | T | 24 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
31 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.493-20A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 4/11 | chr1 | 47084600 | |||||||
| chr1:47084752 | A | G | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0163 others(8): Show |
15 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.617+8A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 5/11 | chr1 | 47084752 | |||||||
| chr1:47084753 | C | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0163 others(8): Show |
15 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.617+9C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 5/11 | chr1 | 47084753 | |||||||
| chr1:47085095 | A | G | 65 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(62): Show |
93 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.772+117A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085095 | |||||||
| chr1:47085324 | A | G | 1 | a0006c0006t0001g0162 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.772+346A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085324 | |||||||
| chr1:47085341 | G | C | 1 | a0001c0002t0001g0007 | 5 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.772+363G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085341 | |||||||
| chr1:47085376 | C | T | 6 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(3): Show |
7 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.772+398C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085376 | |||||||
| chr1:47085391 | T | G | 23 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(20): Show |
30 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.772+413T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085391 | |||||||
| chr1:47085575 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.772+597A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085575 | |||||||
| chr1:47085601 | G | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(80): Show |
119 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.772+623G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085601 | |||||||
| chr1:47085666 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
5 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.772+688G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085666 | |||||||
| chr1:47085667 | G | A | 3 | a0001c0002t0001g0058 a0001c0002t0001g0090 a0001c0002t0001g0097 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.772+689G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085667 | |||||||
| chr1:47085786 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.772+808T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085786 | |||||||
| chr1:47085788 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.772+810C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085788 | |||||||
| chr1:47085810 | C | G | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.772+832C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085810 | |||||||
| chr1:47085839 | C | A | 2 | a0001c0002t0001g0022 a0001c0002t0001g0065 |
3 | HG00735.hp1 HG01169.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.772+861C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085839 | |||||||
| chr1:47085843 | C | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.772+865C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085843 | |||||||
| chr1:47085897 | A | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0117 a0005c0007t0001g0115 |
4 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.772+919A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085897 | |||||||
| chr1:47085920 | A | G | 1 | a0001c0002t0001g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.772+942A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085920 | |||||||
| chr1:47085934 | A | C | 1 | a0001c0002t0001g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.772+956A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085934 | |||||||
| chr1:47085939 | C | T | 1 | a0001c0002t0001g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.772+961C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085939 | |||||||
| chr1:47085985 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.772+1007C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47085985 | |||||||
| chr1:47086065 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.772+1087T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086065 | |||||||
| chr1:47086085 | G | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(7): Show |
13 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.772+1107G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086085 | |||||||
| chr1:47086108 | C | G | 1 | a0001c0002t0001g0061 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.772+1130C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086108 | |||||||
| chr1:47086176 | C | T | 1 | a0001c0002t0001g0081 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.772+1198C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086176 | |||||||
| chr1:47086358 | G | C | 66 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(63): Show |
94 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.772+1380G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086358 | |||||||
| chr1:47086374 | A | G | 2 | a0001c0002t0001g0052 a0001c0002t0001g0053 |
2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.772+1396A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086374 | |||||||
| chr1:47086380 | G | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0123 a0001c0001t0001g0127 others(4): Show |
8 | HG00408.hp1 HG00609.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.772+1402G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086380 | |||||||
| chr1:47086469 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.772+1491T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086469 | |||||||
| chr1:47086642 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.772+1664C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086642 | |||||||
| chr1:47086659 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0206 |
4 | HG01261.hp1 HG01496.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.772+1681T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086659 | |||||||
| chr1:47086660 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.772+1682G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086660 | |||||||
| chr1:47086668 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.772+1690C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086668 | |||||||
| chr1:47086676 | G | T | 1 | a0005c0007t0001g0115 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.772+1698G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086676 | |||||||
| chr1:47086704 | C | T | 1 | a0001c0002t0001g0029 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.772+1726C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086704 | |||||||
| chr1:47086858 | A | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(18): Show |
28 | HG00280.hp2 HG00408.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.772+1880A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086858 | |||||||
| chr1:47086872 | A | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG00639.hp1 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.772+1894A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086872 | |||||||
| chr1:47086904 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.772+1926C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47086904 | |||||||
| chr1:47087125 | T | C | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(67): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.772+2147T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087125 | |||||||
| chr1:47087127 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.772+2149T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087127 | |||||||
| chr1:47087139 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.772+2161G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087139 | |||||||
| chr1:47087158 | A | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.772+2180A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087158 | |||||||
| chr1:47087258 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.772+2280G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087258 | |||||||
| chr1:47087268 | G | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.772+2290G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087268 | |||||||
| chr1:47087320 | C | T | 1 | a0001c0002t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.772+2342C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087320 | |||||||
| chr1:47087325 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.772+2347G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087325 | |||||||
| chr1:47087342 | C | T | 5 | a0001c0002t0001g0092 a0001c0002t0001g0093 a0001c0008t0001g0091 others(2): Show |
5 | HG02258.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.772+2364C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087342 | |||||||
| chr1:47087418 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.772+2440G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087418 | |||||||
| chr1:47087455 | C | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.772+2477C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087455 | |||||||
| chr1:47087684 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0166 |
4 | NA18939.hp2 NA18982.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.772+2706A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087684 | |||||||
| chr1:47087844 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.772+2866C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087844 | |||||||
| chr1:47087862 | A | G | 1 | a0001c0002t0001g0066 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.772+2884A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087862 | |||||||
| chr1:47087996 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.772+3018T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47087996 | |||||||
| chr1:47088067 | C | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.772+3089C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088067 | |||||||
| chr1:47088081 | G | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.772+3103G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088081 | |||||||
| chr1:47088090 | C | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.772+3112C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088090 | |||||||
| chr1:47088137 | G | A | 3 | a0001c0002t0001g0058 a0001c0002t0001g0090 a0001c0002t0001g0097 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.772+3159G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088137 | |||||||
| chr1:47088373 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.772+3395G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088373 | |||||||
| chr1:47088524 | G | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.772+3546G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088524 | |||||||
| chr1:47088561 | T | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.772+3583T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088561 | |||||||
| chr1:47088777 | C | T | 2 | a0001c0002t0001g0079 a0001c0002t0001g0092 |
2 | HG01975.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.772+3799C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088777 | |||||||
| chr1:47088778 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.772+3800G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088778 | |||||||
| chr1:47088791 | A | AT | 2 | a0001c0001t0001g0055 a0001c0002t0001g0007 |
6 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.772+3823dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47088791 | ||||||
| chr1:47088808 | G | T | 3 | a0001c0002t0001g0058 a0001c0002t0001g0090 a0001c0002t0001g0097 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.772+3830G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088808 | |||||||
| chr1:47088920 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.772+3942C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088920 | |||||||
| chr1:47088979 | A | C | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(68): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.772+4001A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47088979 | |||||||
| chr1:47089052 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(3): Show |
8 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.772+4074C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089052 | |||||||
| chr1:47089181 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.772+4203C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089181 | |||||||
| chr1:47089185 | A | T | 1 | a0001c0002t0001g0098 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.772+4207A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089185 | |||||||
| chr1:47089260 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(80): Show |
119 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.772+4282C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089260 | |||||||
| chr1:47089414 | A | G | 1 | a0001c0002t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.772+4436A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089414 | |||||||
| chr1:47089528 | CACCTAAT others(8): Show |
C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
31 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.772+4554_772+4568d others(17): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47089528 | ||||||
| chr1:47089543 | A | C | 1 | a0001c0002t0001g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.772+4565A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089543 | |||||||
| chr1:47089600 | T | G | 1 | a0001c0001t0001g0166 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.772+4622T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089600 | |||||||
| chr1:47089636 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0127 |
3 | HG02074.hp1 NA18747.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.772+4658T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089636 | |||||||
| chr1:47089781 | A | G | 1 | a0001c0001t0001g0041 | 2 | HG02109.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.773-4785A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089781 | |||||||
| chr1:47089830 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(7): Show |
13 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.773-4736A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089830 | |||||||
| chr1:47089958 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-4608T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47089958 | |||||||
| chr1:47090026 | T | C | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.773-4540T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090026 | |||||||
| chr1:47090087 | G | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(76): Show |
114 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.773-4479G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090087 | |||||||
| chr1:47090169 | A | T | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.773-4397A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090169 | |||||||
| chr1:47090236 | T | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.773-4330T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090236 | |||||||
| chr1:47090276 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.773-4290G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090276 | |||||||
| chr1:47090292 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.773-4274C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090292 | |||||||
| chr1:47090319 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.773-4247T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090319 | |||||||
| chr1:47090551 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.773-4015A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090551 | |||||||
| chr1:47090624 | G | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.773-3942G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090624 | |||||||
| chr1:47090770 | C | CTTGAGTG others(4): Show |
67 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(64): Show |
95 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.773-3795_773-3785d others(13): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47090770 | ||||||
| chr1:47090816 | T | C | 3 | a0001c0002t0001g0074 a0001c0002t0001g0079 a0001c0002t0001g0080 |
3 | HG01975.hp1 HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.773-3750T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090816 | |||||||
| chr1:47090908 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.773-3658C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47090908 | |||||||
| chr1:47091045 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.773-3521T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091045 | |||||||
| chr1:47091217 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(68): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.773-3349A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091217 | |||||||
| chr1:47091235 | C | A | 68 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(65): Show |
96 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.773-3331C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091235 | |||||||
| chr1:47091363 | A | G | 70 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(67): Show |
98 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.773-3203A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091363 | |||||||
| chr1:47091431 | A | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.773-3135A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091431 | |||||||
| chr1:47091499 | A | G | 71 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(68): Show |
99 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.773-3067A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091499 | |||||||
| chr1:47091561 | A | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.773-3005A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091561 | |||||||
| chr1:47091573 | C | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.773-2993C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091573 | |||||||
| chr1:47091623 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.773-2943T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091623 | |||||||
| chr1:47091639 | T | C | 30 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(27): Show |
39 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.773-2927T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091639 | |||||||
| chr1:47091691 | C | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-2875C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091691 | |||||||
| chr1:47091710 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(114): Show |
162 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.773-2856T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091710 | |||||||
| chr1:47091756 | CT | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(35): Show |
57 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.773-2802delT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47091756 | ||||||
| chr1:47091775 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.773-2791C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091775 | |||||||
| chr1:47091777 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-2789G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091777 | |||||||
| chr1:47091843 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-2723T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091843 | |||||||
| chr1:47091851 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-2715C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091851 | |||||||
| chr1:47091877 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.773-2689C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091877 | |||||||
| chr1:47091882 | C | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(37): Show |
59 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.773-2684C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091882 | |||||||
| chr1:47091887 | G | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.773-2679G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091887 | |||||||
| chr1:47091909 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.773-2657G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091909 | |||||||
| chr1:47091952 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG02109.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.773-2614G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091952 | |||||||
| chr1:47091958 | T | C | 24 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(21): Show |
31 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.773-2608T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091958 | |||||||
| chr1:47091984 | C | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(34): Show |
56 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.773-2582C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47091984 | |||||||
| chr1:47092004 | A | C | 2 | a0001c0001t0001g0112 a0001c0002t0001g0089 |
2 | HG01175.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.773-2562A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092004 | |||||||
| chr1:47092040 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-2526T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092040 | |||||||
| chr1:47092119 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.773-2447T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092119 | |||||||
| chr1:47092120 | C | G | 9 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(6): Show |
11 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.773-2446C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092120 | |||||||
| chr1:47092128 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.773-2438A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092128 | |||||||
| chr1:47092191 | A | C | 13 | a0001c0001t0001g0055 a0001c0002t0001g0007 a0001c0002t0001g0049 others(10): Show |
18 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.773-2375A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092191 | |||||||
| chr1:47092235 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-2331C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092235 | |||||||
| chr1:47092261 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-2305T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092261 | |||||||
| chr1:47092261 | T | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(75): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.773-2305T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092261 | |||||||
| chr1:47092297 | C | CT | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-2267dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47092297 | ||||||
| chr1:47092312 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.773-2254C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092312 | |||||||
| chr1:47092348 | A | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG00642.hp2 HG01884.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.773-2218A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092348 | |||||||
| chr1:47092457 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.773-2109G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092457 | |||||||
| chr1:47092482 | C | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(9): Show |
15 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.773-2084C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092482 | |||||||
| chr1:47092486 | C | T | 12 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(9): Show |
15 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.773-2080C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092486 | |||||||
| chr1:47092661 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.773-1905A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092661 | |||||||
| chr1:47092751 | A | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0118 others(6): Show |
12 | HG01070.hp1 HG01081.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.773-1815A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092751 | |||||||
| chr1:47092783 | A | G | 12 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(9): Show |
15 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.773-1783A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092783 | |||||||
| chr1:47092918 | C | A | 1 | a0001c0001t0001g0169 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.773-1648C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47092918 | |||||||
| chr1:47093032 | G | C | 1 | a0001c0001t0001g0131 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.773-1534G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093032 | |||||||
| chr1:47093047 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.773-1519T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093047 | |||||||
| chr1:47093050 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.773-1516T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093050 | |||||||
| chr1:47093127 | AAAG | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-1435_773-1433d others(5): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47093127 | ||||||
| chr1:47093321 | A | C | 9 | a0001c0001t0001g0055 a0001c0001t0001g0112 a0001c0001t0001g0118 others(6): Show |
9 | HG01433.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.773-1245A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093321 | |||||||
| chr1:47093459 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-1107G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093459 | |||||||
| chr1:47093580 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.773-986G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093580 | |||||||
| chr1:47093588 | T | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-978T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093588 | |||||||
| chr1:47093873 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-693G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093873 | |||||||
| chr1:47093893 | A | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-673A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093893 | |||||||
| chr1:47093964 | A | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-602A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47093964 | |||||||
| chr1:47094122 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-444T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094122 | |||||||
| chr1:47094127 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-439C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094127 | |||||||
| chr1:47094161 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.773-405G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094161 | |||||||
| chr1:47094217 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(40): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.773-349G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094217 | |||||||
| chr1:47094344 | A | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-222A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094344 | |||||||
| chr1:47094350 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-216C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094350 | |||||||
| chr1:47094367 | G | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(145): Show |
212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.773-199G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094367 | |||||||
| chr1:47094385 | T | TGAAGTAC others(10): Show |
3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-180_773-179ins others(17): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 47094385 | ||||||
| chr1:47094396 | G | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.773-170G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094396 | |||||||
| chr1:47094514 | T | C | 1 | a0004c0011t0001g0085 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.773-52T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 6/11 | chr1 | 47094514 | |||||||
| chr1:47094772 | C | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.876+103C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47094772 | |||||||
| chr1:47094883 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.876+214T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47094883 | |||||||
| chr1:47094934 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.876+265G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47094934 | |||||||
| chr1:47095017 | A | G | 1 | a0001c0002t0001g0089 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.876+348A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095017 | |||||||
| chr1:47095044 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+375A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095044 | |||||||
| chr1:47095068 | C | CT | 31 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0039 others(28): Show |
42 | HG00423.hp2 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.876+401dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47095068 | ||||||
| chr1:47095316 | G | GA | 9 | a0001c0001t0001g0084 a0001c0002t0001g0009 a0001c0002t0001g0026 others(6): Show |
13 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.876+652dupA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47095316 | ||||||
| chr1:47095321 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.876+652A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095321 | |||||||
| chr1:47095393 | T | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0047 others(1): Show |
6 | HG00738.hp1 HG02109.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.876+724T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095393 | |||||||
| chr1:47095446 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.876+777A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095446 | |||||||
| chr1:47095519 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.876+850A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095519 | |||||||
| chr1:47095531 | A | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+862A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095531 | |||||||
| chr1:47095581 | T | A | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.876+912T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095581 | |||||||
| chr1:47095660 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.876+991G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095660 | |||||||
| chr1:47095928 | C | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+1259C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095928 | |||||||
| chr1:47095939 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+1270T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095939 | |||||||
| chr1:47095941 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+1272G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095941 | |||||||
| chr1:47095947 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+1278C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095947 | |||||||
| chr1:47095955 | G | GA | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+1287dupA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47095955 | ||||||
| chr1:47095958 | C | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+1289C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47095958 | |||||||
| chr1:47096035 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.876+1366A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096035 | |||||||
| chr1:47096083 | A | G | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(6): Show |
12 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.876+1414A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096083 | |||||||
| chr1:47096127 | T | A | 1 | a0001c0001t0002g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.876+1458T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096127 | |||||||
| chr1:47096161 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.876+1492G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096161 | |||||||
| chr1:47096414 | G | A | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(6): Show |
12 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.876+1745G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096414 | |||||||
| chr1:47096415 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+1746T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096415 | |||||||
| chr1:47096616 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.876+1947T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096616 | |||||||
| chr1:47096629 | C | CT | 9 | a0001c0002t0001g0009 a0001c0002t0001g0026 a0001c0002t0001g0027 others(6): Show |
13 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.876+1979dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47096629 | ||||||
| chr1:47096629 | CT | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
184 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.876+1979delT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47096629 | ||||||
| chr1:47096629 | CTT | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(12): Show |
22 | HG01169.hp2 HG01261.hp1 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.876+1978_876+1979d others(4): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47096629 | ||||||
| chr1:47096707 | C | G | 5 | a0001c0002t0001g0009 a0001c0002t0001g0027 a0001c0002t0001g0062 others(2): Show |
8 | HG01243.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.876+2038C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096707 | |||||||
| chr1:47096715 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.876+2046A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096715 | |||||||
| chr1:47096867 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.876+2198T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096867 | |||||||
| chr1:47096898 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877-2196A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096898 | |||||||
| chr1:47096958 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.877-2136C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47096958 | |||||||
| chr1:47097001 | C | T | 1 | a0001c0002t0001g0069 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.877-2093C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097001 | |||||||
| chr1:47097031 | C | T | 1 | a0001c0002t0001g0029 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.877-2063C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097031 | |||||||
| chr1:47097120 | T | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0084 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.877-1974T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097120 | |||||||
| chr1:47097160 | G | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.877-1934G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097160 | |||||||
| chr1:47097180 | T | C | 1 | a0001c0002t0001g0081 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.877-1914T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097180 | |||||||
| chr1:47097216 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877-1878C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097216 | |||||||
| chr1:47097512 | C | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877-1582C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097512 | |||||||
| chr1:47097561 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(93): Show |
135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.877-1533G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097561 | |||||||
| chr1:47097709 | A | G | 1 | a0001c0002t0001g0078 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.877-1385A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097709 | |||||||
| chr1:47097725 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.877-1369T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097725 | |||||||
| chr1:47097745 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(32): Show |
54 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.877-1349G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097745 | |||||||
| chr1:47097745 | G | T | 1 | a0001c0001t0001g0202 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.877-1349G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097745 | |||||||
| chr1:47097808 | C | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877-1286C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097808 | |||||||
| chr1:47097820 | A | AT | 18 | a0001c0001t0001g0055 a0001c0001t0001g0127 a0001c0001t0001g0144 others(15): Show |
25 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.877-1257dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47097820 | ||||||
| chr1:47097820 | A | ATT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(95): Show |
141 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.877-1258_877-1257d others(4): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47097820 | ||||||
| chr1:47097820 | A | ATTT | 46 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(43): Show |
67 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.877-1259_877-1257d others(5): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47097820 | ||||||
| chr1:47097820 | A | ATTTT | 8 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0179 others(5): Show |
8 | HG00423.hp1 HG01109.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.877-1260_877-1257d others(6): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 47097820 | ||||||
| chr1:47097909 | A | G | 1 | a0001c0002t0001g0025 | 2 | HG02280.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.877-1185A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097909 | |||||||
| chr1:47097975 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0117 a0005c0007t0001g0115 |
4 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.877-1119C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47097975 | |||||||
| chr1:47098062 | C | A | 1 | a0001c0002t0001g0070 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.877-1032C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098062 | |||||||
| chr1:47098069 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(79): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.877-1025G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098069 | |||||||
| chr1:47098094 | A | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.877-1000A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098094 | |||||||
| chr1:47098095 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.877-999G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098095 | |||||||
| chr1:47098095 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.877-999G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098095 | |||||||
| chr1:47098096 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877-998C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098096 | |||||||
| chr1:47098104 | G | A | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0124 others(9): Show |
16 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.877-990G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098104 | |||||||
| chr1:47098228 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.877-866T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098228 | |||||||
| chr1:47098236 | C | A | 1 | a0001c0002t0001g0076 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.877-858C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098236 | |||||||
| chr1:47098318 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.877-776C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098318 | |||||||
| chr1:47098338 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.877-756C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098338 | |||||||
| chr1:47098604 | A | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0189 a0001c0001t0001g0190 |
4 | NA18970.hp2 NA18980.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.877-490A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098604 | |||||||
| chr1:47098640 | T | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.877-454T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098640 | |||||||
| chr1:47098826 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877-268T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098826 | |||||||
| chr1:47098859 | G | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(79): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.877-235G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098859 | |||||||
| chr1:47098874 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877-220A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098874 | |||||||
| chr1:47098915 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.877-179C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47098915 | |||||||
| chr1:47099064 | T | A | 1 | a0001c0001t0001g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.877-30T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 7/11 | chr1 | 47099064 | |||||||
| chr1:47099359 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1067+75A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099359 | |||||||
| chr1:47099373 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1067+89T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099373 | |||||||
| chr1:47099446 | G | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(6): Show |
12 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1067+162G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099446 | |||||||
| chr1:47099465 | C | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0211 a0001c0001t0001g0212 |
5 | NA18979.hp1 NA18982.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1067+181C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099465 | |||||||
| chr1:47099744 | A | G | 8 | a0001c0001t0001g0111 a0001c0001t0001g0114 a0001c0001t0001g0120 others(5): Show |
8 | HG01943.hp2 HG02257.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067+460A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099744 | |||||||
| chr1:47099805 | A | G | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(41): Show |
65 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1067+521A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099805 | |||||||
| chr1:47099870 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1067+586T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099870 | |||||||
| chr1:47099934 | T | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1067+650T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099934 | |||||||
| chr1:47099936 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1067+652A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099936 | |||||||
| chr1:47099953 | A | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1067+669A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099953 | |||||||
| chr1:47099990 | A | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1067+706A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47099990 | |||||||
| chr1:47100023 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1067+739A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100023 | |||||||
| chr1:47100029 | A | G | 10 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0105 others(7): Show |
13 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1067+745A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100029 | |||||||
| chr1:47100033 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1067+749A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100033 | |||||||
| chr1:47100068 | T | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1067+784T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100068 | |||||||
| chr1:47100266 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1067+982A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100266 | |||||||
| chr1:47100485 | G | T | 1 | a0001c0001t0001g0174 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1067+1201G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100485 | |||||||
| chr1:47100621 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1067+1337C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100621 | |||||||
| chr1:47100826 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+1542C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100826 | |||||||
| chr1:47100849 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(75): Show |
113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1067+1565C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100849 | |||||||
| chr1:47100919 | G | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+1635G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100919 | |||||||
| chr1:47100920 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+1636C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47100920 | |||||||
| chr1:47101045 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+1761C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101045 | |||||||
| chr1:47101093 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1067+1809A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101093 | |||||||
| chr1:47101229 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1067+1945T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101229 | |||||||
| chr1:47101317 | TA | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(33): Show |
55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1067+2034delA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101317 | |||||||
| chr1:47101529 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1067+2245G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101529 | |||||||
| chr1:47101618 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1067+2334A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101618 | |||||||
| chr1:47101677 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1067+2393A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101677 | |||||||
| chr1:47101825 | T | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(79): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1067+2541T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101825 | |||||||
| chr1:47101868 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0117 a0005c0007t0001g0115 |
4 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1067+2584G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101868 | |||||||
| chr1:47101877 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+2593G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101877 | |||||||
| chr1:47101883 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+2599G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47101883 | |||||||
| chr1:47102033 | T | C | 1 | a0001c0002t0001g0058 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1067+2749T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102033 | |||||||
| chr1:47102035 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+2751C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102035 | |||||||
| chr1:47102067 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1067+2783C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102067 | |||||||
| chr1:47102227 | G | T | 1 | a0001c0002t0001g0080 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1067+2943G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102227 | |||||||
| chr1:47102261 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0140 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1067+2977T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102261 | |||||||
| chr1:47102382 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1067+3098C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102382 | |||||||
| chr1:47102488 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1067+3204T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102488 | |||||||
| chr1:47102533 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1067+3249G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102533 | |||||||
| chr1:47102701 | G | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0116 a0001c0001t0001g0117 others(1): Show |
5 | HG01943.hp1 HG02647.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1067+3417G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102701 | |||||||
| chr1:47102752 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1068-3376C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102752 | |||||||
| chr1:47102839 | T | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1068-3289T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102839 | |||||||
| chr1:47102859 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1068-3269G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102859 | |||||||
| chr1:47102882 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1068-3246T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47102882 | |||||||
| chr1:47103033 | A | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(79): Show |
118 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1068-3095A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103033 | |||||||
| chr1:47103202 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1068-2926G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103202 | |||||||
| chr1:47103256 | T | C | 15 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0055 others(12): Show |
18 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1068-2872T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103256 | |||||||
| chr1:47103258 | C | A | 2 | a0003c0004t0001g0094 a0003c0004t0001g0095 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1068-2870C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103258 | |||||||
| chr1:47103273 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1068-2855G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103273 | |||||||
| chr1:47103280 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1068-2848A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103280 | |||||||
| chr1:47103346 | AT | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(71): Show |
102 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1068-2771delT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47103346 | ||||||
| chr1:47103377 | A | G | 13 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0084 others(10): Show |
16 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1068-2751A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103377 | |||||||
| chr1:47103551 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1068-2577C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103551 | |||||||
| chr1:47103568 | CCTT | C | 5 | a0001c0002t0001g0049 a0001c0002t0001g0051 a0001c0002t0001g0052 others(2): Show |
6 | HG02280.hp1 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1068-2553_1068-255 others(7): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47103568 | ||||||
| chr1:47103575 | C | CT | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068-2543dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47103575 | ||||||
| chr1:47103595 | C | CT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(32): Show |
54 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.1068-2516dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47103595 | ||||||
| chr1:47103595 | CT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(93): Show |
138 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1068-2516delT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47103595 | ||||||
| chr1:47103595 | CTT | C | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(9): Show |
15 | HG01943.hp1 HG02055.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1068-2517_1068-251 others(6): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47103595 | ||||||
| chr1:47103600 | T | C | 1 | a0001c0001t0002g0208 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1068-2528T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103600 | |||||||
| chr1:47103620 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1068-2508G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103620 | |||||||
| chr1:47103634 | G | A | 4 | a0001c0002t0001g0011 a0001c0002t0001g0023 a0001c0002t0001g0081 others(1): Show |
7 | HG01081.hp2 HG01106.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1068-2494G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103634 | |||||||
| chr1:47103652 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1068-2476T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103652 | |||||||
| chr1:47103899 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-2229A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103899 | |||||||
| chr1:47103900 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-2228T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103900 | |||||||
| chr1:47103901 | ATTT | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-2225_1068-222 others(7): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47103901 | ||||||
| chr1:47103972 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-2156A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47103972 | |||||||
| chr1:47104013 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-2115G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104013 | |||||||
| chr1:47104176 | G | A | 1 | a0001c0005t0001g0021 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1068-1952G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104176 | |||||||
| chr1:47104216 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1068-1912A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104216 | |||||||
| chr1:47104263 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1865T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104263 | |||||||
| chr1:47104279 | C | T | 1 | a0001c0002t0001g0007 | 5 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1068-1849C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104279 | |||||||
| chr1:47104284 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1068-1844G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104284 | |||||||
| chr1:47104361 | C | T | 4 | a0001c0002t0001g0010 a0001c0002t0001g0029 a0001c0002t0001g0086 others(1): Show |
7 | HG01257.hp1 HG01258.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1068-1767C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104361 | |||||||
| chr1:47104369 | G | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0143 a0001c0001t0001g0153 |
4 | HG01074.hp1 HG01928.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068-1759G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104369 | |||||||
| chr1:47104386 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1742T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104386 | |||||||
| chr1:47104406 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1722A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104406 | |||||||
| chr1:47104422 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1706C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104422 | |||||||
| chr1:47104468 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1660T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104468 | |||||||
| chr1:47104491 | C | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1637C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104491 | |||||||
| chr1:47104498 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1630A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104498 | |||||||
| chr1:47104618 | C | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1510C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104618 | |||||||
| chr1:47104642 | T | C | 1 | a0001c0005t0001g0021 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1068-1486T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104642 | |||||||
| chr1:47104726 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1068-1402G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104726 | |||||||
| chr1:47104740 | T | C | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1068-1388T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104740 | |||||||
| chr1:47104845 | C | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1068-1283C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104845 | |||||||
| chr1:47104917 | C | CT | 6 | a0001c0002t0001g0059 a0001c0002t0001g0067 a0001c0002t0001g0068 others(3): Show |
6 | HG00738.hp2 HG01175.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.1068-1201dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47104917 | ||||||
| chr1:47104917 | CT | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1201delT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47104917 | ||||||
| chr1:47104931 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1197G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104931 | |||||||
| chr1:47104956 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-1172G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47104956 | |||||||
| chr1:47105100 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1068-1028G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105100 | |||||||
| chr1:47105134 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-994G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105134 | |||||||
| chr1:47105187 | CA | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(93): Show |
135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1068-940delA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105187 | |||||||
| chr1:47105188 | A | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(55): Show |
84 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.1068-940A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105188 | |||||||
| chr1:47105192 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(93): Show |
135 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1068-936G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105192 | |||||||
| chr1:47105294 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-834A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105294 | |||||||
| chr1:47105344 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1068-784G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105344 | |||||||
| chr1:47105373 | C | G | 1 | a0001c0001t0001g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1068-755C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105373 | |||||||
| chr1:47105399 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1068-729C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105399 | |||||||
| chr1:47105402 | C | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-726C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105402 | |||||||
| chr1:47105404 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-724G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105404 | |||||||
| chr1:47105416 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1068-712T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105416 | |||||||
| chr1:47105462 | T | C | 13 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0084 others(10): Show |
16 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1068-666T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105462 | |||||||
| chr1:47105507 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1068-621C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105507 | |||||||
| chr1:47105549 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1068-579T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105549 | |||||||
| chr1:47105566 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1068-562G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105566 | |||||||
| chr1:47105581 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG01884.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1068-547C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105581 | |||||||
| chr1:47105583 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1068-545C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105583 | |||||||
| chr1:47105613 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1068-515C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105613 | |||||||
| chr1:47105647 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-481G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105647 | |||||||
| chr1:47105719 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-409G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105719 | |||||||
| chr1:47105832 | T | A | 1 | a0001c0002t0001g0051 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1068-296T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105832 | |||||||
| chr1:47105832 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-296T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105832 | |||||||
| chr1:47105864 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1068-264C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105864 | |||||||
| chr1:47105918 | CGG | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1068-202_1068-201d others(4): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 47105918 | ||||||
| chr1:47105929 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(152): Show |
221 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1068-199G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47105929 | |||||||
| chr1:47106069 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1068-59T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 8/11 | chr1 | 47106069 | |||||||
| chr1:47106267 | AAAACTTT others(21): Show |
A | 1 | a0006c0006t0001g0162 | 1 | NA18975.hp1 | splice_region_variant&intron_variant | LOW | c.1201+8_1201+35delA others(27): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47106267 | ||||||
| chr1:47106271 | C | CT | 16 | a0001c0002t0001g0003 a0001c0002t0001g0006 a0001c0002t0001g0024 others(13): Show |
22 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1201+26dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47106271 | ||||||
| chr1:47106271 | CTTT | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
212 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1201+24_1201+26del others(3): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47106271 | ||||||
| chr1:47106324 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+63T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106324 | |||||||
| chr1:47106374 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1201+113C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106374 | |||||||
| chr1:47106407 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1201+146T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106407 | |||||||
| chr1:47106426 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1201+165C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106426 | |||||||
| chr1:47106445 | C | G | 3 | a0001c0001t0001g0055 a0001c0001t0001g0113 a0001c0001t0001g0219 |
3 | HG02818.hp2 HG02976.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1201+184C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106445 | |||||||
| chr1:47106446 | A | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0113 a0001c0001t0001g0219 |
3 | HG02818.hp2 HG02976.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1201+185A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106446 | |||||||
| chr1:47106494 | G | A | 1 | a0001c0005t0001g0021 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1201+233G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106494 | |||||||
| chr1:47106504 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+243G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106504 | |||||||
| chr1:47106515 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+254C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106515 | |||||||
| chr1:47106531 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+270A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106531 | |||||||
| chr1:47106576 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+315C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106576 | |||||||
| chr1:47106731 | G | A | 1 | a0001c0002t0001g0093 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1201+470G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106731 | |||||||
| chr1:47106813 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1201+552G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106813 | |||||||
| chr1:47106830 | T | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(74): Show |
110 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1201+569T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106830 | |||||||
| chr1:47106914 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+653G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106914 | |||||||
| chr1:47106966 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1201+705C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106966 | |||||||
| chr1:47106977 | T | C | 1 | a0001c0002t0001g0092 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1201+716T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47106977 | |||||||
| chr1:47107005 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+744A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107005 | |||||||
| chr1:47107171 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
217 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1201+910G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107171 | |||||||
| chr1:47107182 | T | G | 4 | a0001c0001t0001g0055 a0001c0001t0001g0096 a0001c0001t0001g0113 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201+921T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107182 | |||||||
| chr1:47107273 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+1012C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107273 | |||||||
| chr1:47107441 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1201+1180G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107441 | |||||||
| chr1:47107486 | G | C | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1201+1225G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107486 | |||||||
| chr1:47107503 | C | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+1242C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107503 | |||||||
| chr1:47107504 | A | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+1243A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107504 | |||||||
| chr1:47107534 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+1273G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107534 | |||||||
| chr1:47107682 | C | T | 11 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(8): Show |
19 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.1201+1421C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107682 | |||||||
| chr1:47107715 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1201+1454G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107715 | |||||||
| chr1:47107741 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+1480A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107741 | |||||||
| chr1:47107938 | A | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0084 others(7): Show |
13 | HG00639.hp1 HG01192.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1201+1677A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107938 | |||||||
| chr1:47107973 | T | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(9): Show |
14 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1201+1712T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47107973 | |||||||
| chr1:47108162 | C | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+1901C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108162 | |||||||
| chr1:47108263 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1201+2002C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108263 | |||||||
| chr1:47108297 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+2036T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108297 | |||||||
| chr1:47108308 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+2047C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108308 | |||||||
| chr1:47108332 | C | T | 1 | a0001c0002t0001g0053 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1201+2071C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108332 | |||||||
| chr1:47108384 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1201+2123C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108384 | |||||||
| chr1:47108417 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1201+2156G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108417 | |||||||
| chr1:47108459 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1201+2198A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108459 | |||||||
| chr1:47108494 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+2233G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108494 | |||||||
| chr1:47108548 | C | G | 1 | a0001c0002t0001g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1201+2287C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108548 | |||||||
| chr1:47108559 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1201+2298G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108559 | |||||||
| chr1:47108575 | G | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1201+2314G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108575 | |||||||
| chr1:47108582 | C | T | 1 | a0001c0005t0001g0021 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1201+2321C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108582 | |||||||
| chr1:47108676 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1201+2415G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108676 | |||||||
| chr1:47108680 | A | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0197 |
2 | HG02074.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1201+2419A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108680 | |||||||
| chr1:47108683 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1201+2422T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108683 | |||||||
| chr1:47108691 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+2430T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108691 | |||||||
| chr1:47108818 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+2557C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108818 | |||||||
| chr1:47108955 | T | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(36): Show |
61 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1201+2694T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108955 | |||||||
| chr1:47108978 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+2717A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47108978 | |||||||
| chr1:47109000 | A | G | 5 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(2): Show |
5 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201+2739A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109000 | |||||||
| chr1:47109016 | G | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+2755G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109016 | |||||||
| chr1:47109312 | G | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1201+3051G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109312 | |||||||
| chr1:47109320 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1201+3059A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109320 | |||||||
| chr1:47109431 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3170T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109431 | |||||||
| chr1:47109602 | A | G | 3 | a0001c0002t0001g0058 a0001c0002t0001g0090 a0001c0002t0001g0097 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1201+3341A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109602 | |||||||
| chr1:47109607 | T | C | 4 | a0001c0001t0001g0191 a0001c0001t0001g0197 a0001c0001t0001g0198 others(1): Show |
4 | HG00423.hp1 HG02074.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201+3346T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109607 | |||||||
| chr1:47109616 | G | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1201+3355G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109616 | |||||||
| chr1:47109673 | A | G | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1201+3412A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109673 | |||||||
| chr1:47109774 | C | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3513C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109774 | |||||||
| chr1:47109839 | A | C | 1 | a0001c0002t0001g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1201+3578A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109839 | |||||||
| chr1:47109873 | CAAA | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3625_1201+362 others(7): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47109873 | ||||||
| chr1:47109898 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(83): Show |
122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.1201+3637C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47109898 | |||||||
| chr1:47110016 | T | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3755T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110016 | |||||||
| chr1:47110019 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3758G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110019 | |||||||
| chr1:47110076 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3815G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110076 | |||||||
| chr1:47110082 | G | GGATTATG others(3): Show |
1 | a0001c0002t0001g0007 | 5 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1201+3821_1201+382 others(14): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110082 | |||||||
| chr1:47110082 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3821G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110082 | |||||||
| chr1:47110083 | T | A | 1 | a0001c0002t0001g0007 | 5 | HG02145.hp1 HG02486.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1201+3822T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110083 | |||||||
| chr1:47110125 | C | CAAAAACA others(1): Show |
154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3866_1201+386 others(12): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47110125 | ||||||
| chr1:47110172 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3911A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110172 | |||||||
| chr1:47110191 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3930G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110191 | |||||||
| chr1:47110192 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+3931T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110192 | |||||||
| chr1:47110234 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1201+3973G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110234 | |||||||
| chr1:47110273 | A | C | 2 | a0001c0001t0001g0124 a0001c0010t0001g0121 |
2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1201+4012A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110273 | |||||||
| chr1:47110307 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1201+4046A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110307 | |||||||
| chr1:47110330 | A | G | 2 | a0001c0001t0001g0124 a0001c0010t0001g0121 |
2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1201+4069A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110330 | |||||||
| chr1:47110380 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+4119A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110380 | |||||||
| chr1:47110462 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+4201T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110462 | |||||||
| chr1:47110481 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+4220T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110481 | |||||||
| chr1:47110482 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+4221G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110482 | |||||||
| chr1:47110532 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+4271G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110532 | |||||||
| chr1:47110607 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0206 |
4 | HG01261.hp1 HG01496.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201+4346T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110607 | |||||||
| chr1:47110662 | A | G | 1 | a0001c0002t0001g0077 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1201+4401A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110662 | |||||||
| chr1:47110669 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+4408G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110669 | |||||||
| chr1:47110727 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1201+4466C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110727 | |||||||
| chr1:47110737 | A | C | 4 | a0001c0001t0001g0055 a0001c0001t0001g0096 a0001c0001t0001g0113 others(1): Show |
4 | HG02559.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1201+4476A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110737 | |||||||
| chr1:47110765 | C | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1201+4504C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110765 | |||||||
| chr1:47110794 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1201+4533G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110794 | |||||||
| chr1:47110835 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1201+4574T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110835 | |||||||
| chr1:47110845 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1201+4584G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110845 | |||||||
| chr1:47110948 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1202-4581G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47110948 | |||||||
| chr1:47111019 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1202-4510T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47111019 | |||||||
| chr1:47111064 | A | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1202-4465A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47111064 | |||||||
| chr1:47111090 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1202-4439T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47111090 | |||||||
| chr1:47111191 | A | AT | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(146): Show |
214 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1202-4326dupT | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47111191 | ||||||
| chr1:47111260 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1202-4269T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47111260 | |||||||
| chr1:47111375 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1202-4154G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47111375 | |||||||
| chr1:47111533 | G | A | 2 | a0001c0002t0001g0056 a0001c0002t0001g0073 |
2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1202-3996G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47111533 | |||||||
| chr1:47111704 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1202-3825A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47111704 | |||||||
| chr1:47111982 | A | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0161 |
2 | HG00280.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1202-3547A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47111982 | |||||||
| chr1:47112086 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1202-3443T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112086 | |||||||
| chr1:47112161 | G | C | 1 | a0001c0002t0001g0086 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1202-3368G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112161 | |||||||
| chr1:47112510 | T | C | 10 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0055 others(7): Show |
13 | HG01192.hp2 HG01243.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1202-3019T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112510 | |||||||
| chr1:47112514 | TAACA | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1202-3011_1202-300 others(8): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47112514 | ||||||
| chr1:47112558 | A | T | 1 | a0001c0002t0001g0083 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1202-2971A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112558 | |||||||
| chr1:47112566 | T | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0084 others(5): Show |
10 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1202-2963T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112566 | |||||||
| chr1:47112604 | C | A | 1 | a0001c0008t0001g0091 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1202-2925C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112604 | |||||||
| chr1:47112608 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1202-2921T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112608 | |||||||
| chr1:47112612 | C | G | 3 | a0001c0002t0001g0058 a0001c0002t0001g0090 a0001c0002t0001g0097 |
3 | HG02922.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1202-2917C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112612 | |||||||
| chr1:47112716 | C | CACA | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1202-2811_1202-280 others(7): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47112716 | ||||||
| chr1:47112799 | A | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1202-2730A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112799 | |||||||
| chr1:47112842 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1202-2687C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112842 | |||||||
| chr1:47112995 | T | A | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1202-2534T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47112995 | |||||||
| chr1:47113003 | GA | G | 8 | a0001c0001t0001g0096 a0001c0001t0001g0209 a0001c0002t0001g0079 others(5): Show |
8 | HG01975.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1202-2514delA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47113003 | ||||||
| chr1:47113057 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1202-2472T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113057 | |||||||
| chr1:47113342 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1202-2187T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113342 | |||||||
| chr1:47113429 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1202-2100T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113429 | |||||||
| chr1:47113625 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1202-1904A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113625 | |||||||
| chr1:47113655 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1202-1874G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113655 | |||||||
| chr1:47113664 | G | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(36): Show |
61 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1202-1865G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113664 | |||||||
| chr1:47113775 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1202-1754G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113775 | |||||||
| chr1:47113785 | G | A | 1 | a0001c0002t0001g0028 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1202-1744G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113785 | |||||||
| chr1:47113810 | G | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1202-1719G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113810 | |||||||
| chr1:47113829 | C | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1202-1700C>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113829 | |||||||
| chr1:47113876 | T | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0108 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1202-1653T>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113876 | |||||||
| chr1:47113896 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1202-1633A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113896 | |||||||
| chr1:47113898 | C | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0084 others(5): Show |
10 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1202-1631C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47113898 | |||||||
| chr1:47114113 | A | G | 1 | a0001c0002t0001g0060 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1202-1416A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114113 | |||||||
| chr1:47114416 | A | C | 1 | a0001c0001t0001g0038 | 2 | NA19054.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1202-1113A>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114416 | |||||||
| chr1:47114426 | A | G | 8 | a0001c0001t0001g0034 a0001c0001t0001g0123 a0001c0001t0001g0127 others(5): Show |
9 | HG00408.hp1 HG00609.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-1103A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114426 | |||||||
| chr1:47114473 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1202-1056C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114473 | |||||||
| chr1:47114481 | A | G | 5 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(2): Show |
5 | HG02280.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202-1048A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114481 | |||||||
| chr1:47114498 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1202-1031G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114498 | |||||||
| chr1:47114562 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(36): Show |
61 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.1202-967C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114562 | |||||||
| chr1:47114599 | G | GA | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1202-923dupA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47114599 | ||||||
| chr1:47114634 | AG | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1202-893delG | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47114634 | ||||||
| chr1:47114769 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1202-760A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114769 | |||||||
| chr1:47114772 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1202-757C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114772 | |||||||
| chr1:47114823 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1202-706T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114823 | |||||||
| chr1:47114893 | T | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0209 |
2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1202-636T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114893 | |||||||
| chr1:47114912 | G | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0084 others(5): Show |
10 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1202-617G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114912 | |||||||
| chr1:47114971 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1202-558G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114971 | |||||||
| chr1:47114975 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1202-554C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114975 | |||||||
| chr1:47114996 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0113 |
2 | HG02976.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1202-533C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47114996 | |||||||
| chr1:47115153 | G | A | 4 | a0001c0002t0001g0059 a0001c0002t0001g0067 a0001c0002t0001g0069 others(1): Show |
4 | HG00738.hp2 HG01175.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1202-376G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47115153 | |||||||
| chr1:47115270 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1202-259G>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47115270 | |||||||
| chr1:47115406 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1202-123C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47115406 | |||||||
| chr1:47115450 | A | T | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.1202-79A>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47115450 | |||||||
| chr1:47115467 | G | GA | 7 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0182 others(4): Show |
8 | HG02486.hp1 HG02622.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1202-51dupA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 47115467 | ||||||
| chr1:47115504 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0100 others(4): Show |
9 | HG02055.hp1 HG02257.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-25C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 9/11 | chr1 | 47115504 | |||||||
| chr1:47115717 | CA | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1266+129delA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 47115717 | ||||||
| chr1:47115810 | C | G | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1266+217C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47115810 | |||||||
| chr1:47115862 | C | T | 10 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0210 others(7): Show |
14 | HG00280.hp2 HG00408.hp2 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1266+269C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47115862 | |||||||
| chr1:47116130 | C | T | 1 | a0001c0002t0001g0027 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1267-520C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47116130 | |||||||
| chr1:47116146 | A | G | 2 | a0002c0003t0001g0193 a0002c0003t0001g0196 |
2 | NA18989.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1267-504A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47116146 | |||||||
| chr1:47116474 | T | C | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-176T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47116474 | |||||||
| chr1:47116523 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1267-127G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47116523 | |||||||
| chr1:47116570 | ATTTCGT | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(74): Show |
110 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1267-76_1267-71del others(6): Show |
CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 47116570 | ||||||
| chr1:47116574 | C | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(106): Show |
153 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.1267-76C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47116574 | |||||||
| chr1:47116620 | T | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1267-30T>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47116620 | |||||||
| chr1:47116627 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0113 |
2 | HG02976.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1267-23T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 10/11 | chr1 | 47116627 | |||||||
| chr1:47116943 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1349+211T>C | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47116943 | |||||||
| chr1:47116966 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1349+234G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47116966 | |||||||
| chr1:47117053 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1349+321G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117053 | |||||||
| chr1:47117141 | C | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(37): Show |
62 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.1349+409C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117141 | |||||||
| chr1:47117160 | A | G | 1 | a0001c0005t0001g0021 | 2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1349+428A>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117160 | |||||||
| chr1:47117341 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1350-425C>G | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117341 | |||||||
| chr1:47117478 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1350-288C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117478 | |||||||
| chr1:47117535 | G | A | 1 | a0001c0002t0001g0024 | 2 | HG02630.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1350-231G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117535 | |||||||
| chr1:47117612 | G | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1350-154G>A | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117612 | |||||||
| chr1:47117649 | G | GA | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(74): Show |
110 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1350-108dupA | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 47117649 | ||||||
| chr1:47117743 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
219 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1350-23G>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117743 | |||||||
| chr1:47117760 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01943.hp2 | splice_region_variant&intron_variant | LOW | c.1350-6C>T | CYP4Z1 | ENSG00000186160.5 | transcript | ENST00000334194.4 | protein_coding | 11/11 | chr1 | 47117760 |