Item | Value |
---|---|
geneid | 126410 |
ensemblid | ENSG00000171954.13 |
hgncid | 26820 |
symbol | CYP4F22 |
name | cytochrome P450 family 4 subfamily F member 22 |
refseq_nuc | NM_173483.4 |
refseq_prot | NP_775754.2 |
ensembl_nuc | ENST00000269703.8 |
ensembl_prot | ENSP00000269703.1 |
mane_status | MANE Select |
chr | chr19 |
start | 15508525 |
end | 15552317 |
strand | + |
ver | v1.2 |
region | chr19:15508525-15552317 |
region5000 | chr19:15503525-15557317 |
regionname0 | CYP4F22_chr19_15508525_15552317 |
regionname5000 | CYP4F22_chr19_15503525_15557317 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 531 | 349 | 72 | 74 | 135 | 18 | 48 | 98 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0002 | 0/0 | 531 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0003 | 0/0 | 531 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0004 | 0/0 | 531 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0005 | 0/0 | 531 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0006 | 0/0 | 531 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0007 | 0/0 | 531 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0008 | 0/0 | 531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0009 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0010 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0011 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
a0012 | 0/0 | 531 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | MLPIT others(526): Show |
chr19 | 15503525 | 15557317 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1593 | 316 | 55 | 70 | 127 | 18 | 44 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0001c0002 | 0/0 | 1593 | 17 | 5 | 2 | 6 | 0 | 4 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0001c0004 | 0/0 | 1593 | 9 | 9 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0001c0005 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0001c0011 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0001c0012 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0001c0013 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0001c0020 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0002c0003 | 0/0 | 1593 | 17 | 17 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0003c0007 | 0/0 | 1593 | 3 | 1 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0004c0008 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0005c0006 | 0/0 | 1593 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0006c0016 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0006c0017 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0007c0009 | 0/0 | 1593 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0008c0010 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0009c0019 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0010c0018 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0011c0015 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 | ||
a0012c0014 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | ATGCT others(1588): Show |
chr19 | 15503525 | 15557317 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2608 | 119 | 4 | 20 | 58 | 14 | 22 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0002 | 0/0 | 2608 | 109 | 20 | 18 | 54 | 2 | 15 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0003 | 1/0 | 2608 | 45 | 6 | 23 | 10 | 2 | 3 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0004 | 0/0 | 2608 | 27 | 18 | 7 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0005 | 0/0 | 2609 | 3 | 2 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2604): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0006 | 0/0 | 2609 | 6 | 0 | 2 | 3 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2604): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0007 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0008 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2604): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0009 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2623): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0012 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2623): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0013 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0014 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0001t0015 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0002t0001 | 0/0 | 2608 | 4 | 0 | 0 | 3 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0002t0002 | 0/0 | 2608 | 4 | 1 | 1 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0002t0003 | 0/0 | 2608 | 7 | 3 | 1 | 2 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0002t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0002t0010 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0004t0001 | 0/0 | 2608 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0004t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0004t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0004t0007 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0005t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0005t0004 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0011t0001 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0012t0002 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0013t0001 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0001c0020t0003 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0002c0003t0001 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0002c0003t0002 | 0/0 | 2608 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0002c0003t0003 | 0/0 | 2608 | 5 | 5 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0002c0003t0004 | 0/0 | 2608 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0002c0003t0005 | 0/0 | 2609 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2604): Show |
chr19 | 15503525 | 15557317 |
a0003c0007t0001 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0003c0007t0002 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0003c0007t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0004c0008t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0004c0008t0004 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0005c0006t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0005c0006t0005 | 0/0 | 2609 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2604): Show |
chr19 | 15503525 | 15557317 |
a0006c0016t0005 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2604): Show |
chr19 | 15503525 | 15557317 |
a0006c0017t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0007c0009t0001 | 0/0 | 2608 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0008c0010t0002 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0009c0019t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0010c0018t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0011c0015t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
a0012c0014t0011 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | AGATC others(2603): Show |
chr19 | 15503525 | 15557317 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0012g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0013g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0010g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0005t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0005t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0005t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0011t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0012t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0013t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0020t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0001g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0004g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0003c0007t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0003c0007t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0003c0007t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0004c0008t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0004c0008t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0004c0008t0004g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0005c0006t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0005c0006t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0005c0006t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0006c0016t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0006c0017t0002g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0007c0009t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0007c0009t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0008c0010t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0009c0019t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0010c0018t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0011c0015t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0012c0014t0011g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0360 | EUR | GBR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0365 | EUR | GBR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0357 | EUR | GBR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0355 | EUR | GBR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | FIN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0340 | EUR | FIN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0363 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0150 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0295 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0366 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0232 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0231 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01074 | hp1 | a0001 | c0011 | t0001 | g0312 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0342 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0261 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01109 | hp1 | a0006 | c0016 | t0005 | g0109 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0352 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0368 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0105 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0341 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0344 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0325 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0296 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01361 | hp1 | a0008 | c0010 | t0002 | g0238 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01496 | hp1 | a0001 | c0013 | t0001 | g0359 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0095 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0338 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0369 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0116 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01891 | hp1 | a0001 | c0002 | t0004 | g0331 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0345 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0332 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0350 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02027 | hp1 | a0001 | c0001 | t0015 | g0162 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02040 | hp2 | a0003 | c0007 | t0002 | g0214 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0093 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0347 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02074 | hp1 | a0001 | c0012 | t0002 | g0203 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02083 | hp1 | a0001 | c0002 | t0010 | g0227 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0263 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02257 | hp1 | a0001 | c0005 | t0002 | g0016 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02257 | hp2 | a0009 | c0019 | t0001 | g0146 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0131 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0118 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0317 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02280 | hp2 | a0004 | c0008 | t0004 | g0194 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02451 | hp1 | a0001 | c0004 | t0001 | g0089 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0316 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02572 | hp1 | a0005 | c0006 | t0005 | g0302 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02572 | hp2 | a0003 | c0007 | t0004 | g0097 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02615 | hp1 | a0001 | c0004 | t0007 | g0045 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02615 | hp2 | a0002 | c0003 | t0003 | g0362 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02630 | hp1 | a0002 | c0003 | t0002 | g0007 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0166 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0356 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02717 | hp2 | a0005 | c0006 | t0002 | g0320 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0374 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02723 | hp2 | a0002 | c0003 | t0004 | g0334 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0180 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0330 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02809 | hp2 | a0006 | c0017 | t0002 | g0364 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02818 | hp1 | a0001 | c0004 | t0002 | g0178 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02818 | hp2 | a0002 | c0003 | t0002 | g0361 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0372 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02895 | hp2 | a0001 | c0004 | t0007 | g0092 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02896 | hp1 | a0002 | c0003 | t0004 | g0328 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02897 | hp1 | a0002 | c0003 | t0004 | g0329 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02922 | hp1 | a0005 | c0006 | t0005 | g0009 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02922 | hp2 | a0001 | c0002 | t0003 | g0010 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02965 | hp1 | a0004 | c0008 | t0001 | g0024 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02965 | hp2 | a0002 | c0003 | t0005 | g0314 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02970 | hp2 | a0001 | c0004 | t0004 | g0090 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02976 | hp1 | a0002 | c0003 | t0003 | g0005 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02976 | hp2 | a0002 | c0003 | t0004 | g0098 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0141 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0323 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0310 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03130 | hp1 | a0002 | c0003 | t0005 | g0327 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0091 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0284 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0322 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03225 | hp2 | a0010 | c0018 | t0002 | g0378 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0379 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03486 | hp1 | a0002 | c0003 | t0002 | g0218 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03516 | hp1 | a0001 | c0005 | t0004 | g0018 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0370 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0134 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0343 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0353 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04115 | hp1 | a0001 | c0002 | t0003 | g0264 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0259 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0354 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18522 | hp1 | a0001 | c0005 | t0004 | g0019 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0375 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | CHB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0201 | EAS | CHB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18906 | hp1 | a0011 | c0015 | t0004 | g0205 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0185 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0289 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18952 | hp2 | a0001 | c0001 | t0014 | g0272 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0277 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0271 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18980 | hp1 | a0012 | c0014 | t0011 | g0288 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18983 | hp2 | a0001 | c0020 | t0003 | g0083 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18991 | hp1 | a0003 | c0007 | t0001 | g0281 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0156 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19011 | hp1 | a0007 | c0009 | t0001 | g0229 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19043 | hp1 | a0002 | c0003 | t0003 | g0149 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19043 | hp2 | a0002 | c0003 | t0003 | g0005 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19062 | hp2 | a0007 | c0009 | t0001 | g0228 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0373 | AFR | ASW | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | ASW | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0255 | EUR | TSI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0358 | EUR | TSI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | GIH | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0371 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0324 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0376 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02109 | hp2 | a0004 | c0008 | t0004 | g0377 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02486 | hp1 | a0001 | c0004 | t0007 | g0088 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | USA | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | USA | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20300 | hp1 | a0002 | c0003 | t0003 | g0318 | AFR | USA | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0028 | AFR | USA | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0104 | REF | REF | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0119 | REF | REF | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15537576 | C | T | 1 | a0009 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.463C>T | p.His155Tyr | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 6/14 | 630/2609 | 463/1596 | 155/531 | chr19 | 15537576 | |||
chr19:15537645 | A | T | 3 | a0002 a0006 a0010 |
20 | HG01109.hp1 HG02280.hp1 HG02615.hp2 others(17): Show |
missense_variant | MODERATE | c.532A>T | p.Ser178Cys | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 6/14 | 699/2609 | 532/1596 | 178/531 | chr19 | 15537645 | |||
chr19:15537909 | C | G | 2 | a0004 a0010 |
4 | HG02109.hp2 HG02280.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.587C>G | p.Ser196Cys | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/14 | 754/2609 | 587/1596 | 196/531 | chr19 | 15537909 | |||
chr19:15540512 | A | G | 1 | a0011 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.734A>G | p.Tyr245Cys | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 901/2609 | 734/1596 | 245/531 | chr19 | 15540512 | |||
chr19:15540514 | C | T | 1 | a0003 | 3 | HG02040.hp2 HG02572.hp2 NA18991.hp1 |
missense_variant | MODERATE | c.736C>T | p.Arg246Cys | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 903/2609 | 736/1596 | 246/531 | chr19 | 15540514 | |||
chr19:15540554 | C | G | 1 | a0012 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.776C>G | p.Ala259Gly | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 943/2609 | 776/1596 | 259/531 | chr19 | 15540554 | |||
chr19:15540563 | G | A | 1 | a0008 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.785G>A | p.Arg262Gln | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 952/2609 | 785/1596 | 262/531 | chr19 | 15540563 | |||
chr19:15540628 | C | T | 1 | a0007 | 2 | NA19011.hp1 NA19062.hp2 |
missense_variant | MODERATE | c.850C>T | p.Arg284Trp | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 1017/2609 | 850/1596 | 284/531 | chr19 | 15540628 | |||
chr19:15551388 | A | C | 2 | a0005 a0006 |
5 | HG01109.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
missense_variant | MODERATE | c.1513A>C | p.Lys505Gln | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 1680/2609 | 1513/1596 | 505/531 | chr19 | 15551388 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15525354 | C | T | 1 | a0001c0020 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.18C>T | p.Asp6Asp | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/14 | 185/2609 | 18/1596 | 6/531 | chr19 | 15525354 | |||
chr19:15537560 | T | C | 1 | a0001c0004 | 9 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
synonymous_variant | LOW | c.447T>C | p.Gly149Gly | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 6/14 | 614/2609 | 447/1596 | 149/531 | chr19 | 15537560 | |||
chr19:15537904 | G | A | 1 | a0001c0002 | 17 | HG01243.hp1 HG01256.hp2 HG01891.hp1 others(14): Show |
synonymous_variant | LOW | c.582G>A | p.Ala194Ala | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/14 | 749/2609 | 582/1596 | 194/531 | chr19 | 15537904 | |||
chr19:15540471 | C | T | 1 | a0006c0017 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.693C>T | p.Ser231Ser | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 860/2609 | 693/1596 | 231/531 | chr19 | 15540471 | |||
chr19:15540555 | G | A | 1 | a0001c0005 | 3 | HG02257.hp1 HG03516.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.777G>A | p.Ala259Ala | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 944/2609 | 777/1596 | 259/531 | chr19 | 15540555 | |||
chr19:15540624 | G | A | 1 | a0001c0011 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.846G>A | p.Arg282Arg | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 1013/2609 | 846/1596 | 282/531 | chr19 | 15540624 | |||
chr19:15548111 | C | T | 1 | a0001c0013 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.1140C>T | p.Asp380Asp | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/14 | 1307/2609 | 1140/1596 | 380/531 | chr19 | 15548111 | |||
chr19:15551309 | G | A | 1 | a0001c0012 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.1434G>A | p.Gln478Gln | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 1601/2609 | 1434/1596 | 478/531 | chr19 | 15551309 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15551519 | A | C | 1 | a0001c0001t0015 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*48A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 48 | chr19 | 15551519 | ||||||
chr19:15551561 | C | A | 3 | a0001c0001t0007 a0001c0001t0008 a0001c0004t0007 |
5 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*90C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 90 | chr19 | 15551561 | ||||||
chr19:15551566 | C | G | 1 | a0001c0001t0014 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 95 | chr19 | 15551566 | ||||||
chr19:15551615 | G | A | 1 | a0001c0001t0009 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 144 | chr19 | 15551615 | ||||||
chr19:15551654 | T | G | 44 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(41): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
3_prime_UTR_variant | MODIFIER | c.*183T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 183 | chr19 | 15551654 | ||||||
chr19:15551662 | G | T | 1 | a0001c0001t0013 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 191 | chr19 | 15551662 | ||||||
chr19:15551733 | C | A | 25 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(22): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*262C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 262 | chr19 | 15551733 | ||||||
chr19:15551758 | C | CTCAGGCC others(13): Show |
2 | a0001c0001t0009 a0001c0001t0012 |
2 | HG02258.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*300_*301insTTCTGG others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 301 | INFO_REALIGN_3_PRIME | chr19 | 15551758 | |||||
chr19:15551893 | A | AC | 6 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(3): Show |
15 | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*431dupC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 432 | INFO_REALIGN_3_PRIME | chr19 | 15551893 | |||||
chr19:15551893 | A | C | 1 | a0001c0002t0010 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*422A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 422 | chr19 | 15551893 | ||||||
chr19:15551921 | C | A | 16 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(13): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 450 | chr19 | 15551921 | ||||||
chr19:15552083 | C | A | 1 | a0012c0014t0011 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 612 | chr19 | 15552083 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15508598 | G | GGTGAGGG others(7): Show |
8 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0372 others(5): Show |
8 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+16_-109+29dup others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15508598 | ||||||
chr19:15508726 | AC | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(17): Show |
20 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+150delC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15508726 | ||||||
chr19:15508800 | A | T | 63 | a0001c0001t0001g0321 a0001c0001t0001g0326 a0001c0001t0001g0333 others(60): Show |
64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.-109+217A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508800 | |||||||
chr19:15508827 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+244C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508827 | |||||||
chr19:15508840 | T | C | 2 | a0001c0005t0004g0018 a0001c0005t0004g0019 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+257T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508840 | |||||||
chr19:15508883 | T | G | 9 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0021 others(6): Show |
9 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+300T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508883 | |||||||
chr19:15508992 | C | T | 6 | a0001c0001t0001g0304 a0001c0001t0001g0307 a0001c0001t0001g0309 others(3): Show |
6 | NA18969.hp2 NA18980.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+409C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508992 | |||||||
chr19:15509069 | T | C | 29 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0376 others(26): Show |
29 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-109+486T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509069 | |||||||
chr19:15509398 | G | T | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+815G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509398 | |||||||
chr19:15509505 | G | T | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+922G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509505 | |||||||
chr19:15509623 | G | T | 9 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0021 others(6): Show |
9 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1040G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509623 | |||||||
chr19:15509709 | C | T | 8 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0002g0296 others(5): Show |
8 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+1126C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509709 | |||||||
chr19:15509718 | C | T | 2 | a0001c0001t0002g0290 a0001c0001t0003g0291 |
2 | HG02735.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-109+1135C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509718 | |||||||
chr19:15509765 | C | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(17): Show |
20 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+1182C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509765 | |||||||
chr19:15509802 | C | A | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1219C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509802 | |||||||
chr19:15509854 | C | CTCCT | 52 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0038 others(49): Show |
52 | HG00323.hp1 HG00408.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.-109+1321_-109+132 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | ||||||
chr19:15509854 | C | CTCCTTCC others(1): Show |
34 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(31): Show |
35 | HG00642.hp1 HG01109.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-109+1317_-109+132 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | ||||||
chr19:15509854 | C | CTCCTTCC others(5): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0002g0311 others(6): Show |
9 | HG01074.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1313_-109+132 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | ||||||
chr19:15509854 | C | CTCCTTCC others(9): Show |
1 | a0001c0002t0002g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-109+1309_-109+132 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | ||||||
chr19:15509854 | CTCCT | C | 31 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(28): Show |
31 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-109+1321_-109+132 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | ||||||
chr19:15509854 | CTCCTTCC others(1): Show |
C | 6 | a0001c0001t0001g0177 a0001c0001t0002g0176 a0001c0001t0002g0369 others(3): Show |
6 | HG00738.hp1 HG01884.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+1317_-109+132 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | ||||||
chr19:15509854 | CTCCTTCC others(5): Show |
C | 2 | a0001c0001t0001g0184 a0001c0001t0004g0370 |
2 | HG02683.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-109+1313_-109+132 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | ||||||
chr19:15509889 | C | CTTTCT | 9 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(6): Show |
9 | HG02015.hp2 HG03209.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1308_-109+130 others(9): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509889 | ||||||
chr19:15509889 | C | CTTTCTTT others(2): Show |
25 | a0001c0001t0001g0250 a0001c0001t0001g0253 a0001c0001t0001g0268 others(22): Show |
26 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.-109+1308_-109+130 others(13): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509889 | ||||||
chr19:15509889 | C | CTTTCTTT others(6): Show |
13 | a0001c0001t0001g0246 a0001c0001t0001g0260 a0001c0001t0002g0245 others(10): Show |
13 | HG00558.hp2 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+1308_-109+130 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509889 | ||||||
chr19:15509889 | C | T | 1 | a0001c0002t0003g0289 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-109+1306C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509889 | |||||||
chr19:15509892 | C | CCTTTCTT others(25): Show |
1 | a0001c0001t0004g0231 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-109+1312_-109+131 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509892 | ||||||
chr19:15509892 | C | CCTTTCTT others(29): Show |
1 | a0001c0001t0004g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-109+1312_-109+131 others(40): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509892 | ||||||
chr19:15509892 | C | T | 1 | a0001c0001t0003g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-109+1309C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509892 | |||||||
chr19:15509893 | C | CTTCCTTT others(10): Show |
2 | a0001c0001t0001g0182 a0001c0001t0003g0181 |
2 | HG03834.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-109+1316_-109+131 others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509893 | ||||||
chr19:15509893 | C | CTTTCTTT others(6): Show |
26 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0001g0222 others(23): Show |
26 | HG00323.hp2 HG00621.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.-109+1312_-109+131 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509893 | ||||||
chr19:15509893 | C | T | 35 | a0001c0001t0001g0250 a0001c0001t0001g0253 a0001c0001t0001g0268 others(32): Show |
36 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-109+1310C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509893 | |||||||
chr19:15509896 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0187 a0001c0001t0001g0188 others(40): Show |
44 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.-109+1313C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509896 | |||||||
chr19:15509897 | C | T | 9 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(6): Show |
9 | HG02015.hp2 HG03209.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1314C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509897 | |||||||
chr19:15509900 | C | CCTTTCTT others(9): Show |
3 | a0001c0001t0001g0153 a0001c0001t0003g0154 a0001c0001t0003g0155 |
3 | HG02004.hp2 HG03654.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-109+1320_-109+132 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509900 | ||||||
chr19:15509900 | C | CCTTTCTT others(13): Show |
2 | a0001c0001t0002g0157 a0001c0001t0006g0156 |
2 | HG04228.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-109+1320_-109+132 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509900 | ||||||
chr19:15509900 | C | CCTTTCTT others(17): Show |
1 | a0001c0001t0003g0158 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-109+1320_-109+132 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509900 | ||||||
chr19:15509900 | C | CTTCTTTC others(7): Show |
1 | a0001c0001t0002g0255 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-109+1317_-109+131 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509900 | |||||||
chr19:15509900 | C | CTTT | 7 | a0001c0001t0001g0260 a0001c0001t0002g0256 a0001c0001t0002g0257 others(4): Show |
7 | HG01081.hp2 HG01175.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+1317_-109+131 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509900 | |||||||
chr19:15509900 | C | CTTTCTTT others(4): Show |
2 | a0001c0001t0003g0263 a0001c0002t0003g0264 |
2 | HG02148.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-109+1317_-109+131 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509900 | |||||||
chr19:15509900 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0171 a0001c0001t0001g0173 others(54): Show |
58 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-109+1317C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509900 | |||||||
chr19:15509902 | T | TTTCTTTC others(5): Show |
3 | a0001c0001t0001g0151 a0001c0001t0003g0152 a0001c0001t0006g0150 |
3 | HG00735.hp2 HG01978.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-109+1320_-109+132 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509902 | ||||||
chr19:15509903 | TC | T | 28 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.-109+1322delC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509903 | ||||||
chr19:15509904 | C | CCTTCCTT others(25): Show |
2 | a0001c0001t0001g0135 a0001c0001t0004g0141 |
2 | HG03017.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.-109+1324_-109+132 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CCTTCCTT others(25): Show |
1 | a0001c0001t0002g0127 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-109+1324_-109+132 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CCTTCCTT others(25): Show |
1 | a0001c0001t0005g0134 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-109+1324_-109+132 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CCTTT | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1331_-109+133 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CCTTTCCT others(5): Show |
1 | a0001c0001t0001g0140 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-109+1326_-109+132 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CCTTTCTT others(9): Show |
3 | a0001c0001t0001g0128 a0001c0001t0003g0002 a0001c0001t0004g0132 |
4 | HG01978.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CCTTTCTT others(17): Show |
1 | a0001c0001t0001g0136 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-109+1330_-109+133 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CCTTTCTT others(21): Show |
3 | a0001c0001t0001g0142 a0001c0001t0004g0143 a0001c0001t0004g0144 |
3 | HG01256.hp1 HG01258.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(32): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CCTTTCTT others(25): Show |
2 | a0001c0001t0001g0133 a0001c0001t0002g0147 |
2 | HG00280.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | ||||||
chr19:15509904 | C | CTTT | 22 | a0001c0001t0001g0182 a0001c0001t0001g0219 a0001c0001t0001g0221 others(19): Show |
23 | HG00544.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-109+1321_-109+132 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509904 | |||||||
chr19:15509904 | C | CTTTCTTT others(4): Show |
2 | a0001c0001t0003g0230 a0001c0001t0005g0225 |
2 | HG01257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-109+1321_-109+132 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509904 | |||||||
chr19:15509904 | C | CTTTCTTT others(8): Show |
1 | a0001c0001t0001g0371 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-109+1321_-109+132 others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509904 | |||||||
chr19:15509904 | C | T | 86 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0153 others(83): Show |
87 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-109+1321C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509904 | |||||||
chr19:15509905 | CT | C | 10 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0285 others(7): Show |
10 | HG02015.hp2 HG02976.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.-109+1325delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509905 | ||||||
chr19:15509906 | T | C | 1 | a0001c0001t0003g0244 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-109+1323T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509906 | |||||||
chr19:15509906 | T | TTCCTTCC others(25): Show |
1 | a0001c0001t0002g0101 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-109+1324_-109+132 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | ||||||
chr19:15509906 | T | TTCCTTCC others(17): Show |
2 | a0001c0001t0002g0100 a0001c0001t0002g0102 |
2 | HG02735.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-109+1324_-109+132 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | ||||||
chr19:15509906 | T | TTCCTTCC others(21): Show |
2 | a0001c0001t0001g0001 a0001c0001t0006g0001 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-109+1324_-109+132 others(32): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | ||||||
chr19:15509906 | T | TTCCTTCC others(13): Show |
7 | a0001c0001t0001g0124 a0001c0001t0002g0126 a0001c0001t0002g0129 others(4): Show |
7 | HG01070.hp1 HG01496.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+1324_-109+132 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | ||||||
chr19:15509906 | T | TTTCC | 15 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(12): Show |
15 | HG00544.hp2 HG00609.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+1326_-109+132 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | ||||||
chr19:15509906 | T | TTTCCTTC others(1): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0202 a0001c0001t0001g0206 others(16): Show |
20 | HG00609.hp1 HG00741.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.-109+1326_-109+132 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | ||||||
chr19:15509906 | T | TTTCTTTC others(5): Show |
7 | a0001c0001t0001g0173 a0001c0001t0002g0139 a0001c0001t0002g0172 others(4): Show |
7 | HG01934.hp1 HG02056.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | ||||||
chr19:15509908 | T | C | 42 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0037 others(39): Show |
42 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-109+1325T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509908 | |||||||
chr19:15509910 | T | C | 30 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(27): Show |
30 | HG00544.hp2 HG00609.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-109+1327T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509910 | |||||||
chr19:15509910 | T | TTTCCTTC others(1): Show |
3 | a0001c0001t0001g0171 a0001c0001t0002g0169 a0001c0001t0003g0170 |
3 | HG01168.hp1 HG03579.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509910 | ||||||
chr19:15509914 | T | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0103 a0001c0001t0001g0184 others(25): Show |
28 | HG00741.hp1 HG01074.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.-109+1331T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509914 | |||||||
chr19:15509914 | T | TTTCC | 9 | a0001c0001t0002g0379 a0001c0001t0004g0076 a0001c0001t0004g0077 others(6): Show |
9 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1339_-109+134 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509914 | ||||||
chr19:15509918 | C | CTTCT | 3 | a0001c0001t0002g0106 a0001c0001t0004g0107 a0001c0002t0002g0105 |
3 | HG01243.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-109+1338_-109+133 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509918 | ||||||
chr19:15509918 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(178): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.-109+1335C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509918 | |||||||
chr19:15509922 | C | CTCTTCTT others(11): Show |
1 | a0001c0001t0002g0108 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-109+1340_-109+134 others(22): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCCTTC others(5): Show |
5 | a0001c0001t0002g0015 a0001c0001t0004g0011 a0001c0001t0004g0013 others(2): Show |
5 | HG02622.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+1342_-109+134 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCTTTC others(1): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0041 others(3): Show |
6 | HG01975.hp2 HG03471.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+1358_-109+136 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCTTTC others(5): Show |
20 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG00408.hp2 HG00673.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+1354_-109+136 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCTTTC others(9): Show |
6 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0063 others(3): Show |
6 | HG02055.hp2 HG02602.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+1350_-109+136 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCTTTC others(13): Show |
3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0002g0058 |
3 | HG01515.hp1 HG01517.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-109+1346_-109+136 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCTTTC others(17): Show |
5 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(2): Show |
5 | HG00642.hp2 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+1342_-109+136 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCTTTC others(21): Show |
1 | a0001c0001t0003g0050 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-109+1365_-109+136 others(32): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCTTTC others(25): Show |
3 | a0001c0001t0002g0049 a0001c0001t0002g0290 a0001c0001t0002g0369 |
3 | HG01884.hp1 HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-109+1365_-109+136 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | CTTCTTTC others(33): Show |
2 | a0001c0001t0001g0103 a0006c0016t0005g0109 |
2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-109+1365_-109+136 others(44): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | ||||||
chr19:15509922 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0124 others(176): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.-109+1339C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509922 | |||||||
chr19:15509926 | T | C | 14 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0021 others(11): Show |
14 | HG00621.hp2 HG01891.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-109+1343T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509926 | |||||||
chr19:15509930 | T | C | 2 | a0002c0003t0002g0007 a0002c0003t0002g0008 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-109+1347T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509930 | |||||||
chr19:15509946 | T | TTTCTTTC others(12): Show |
1 | a0001c0001t0002g0048 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-109+1365_-109+136 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509946 | ||||||
chr19:15509947 | T | TTCTTTCT others(27): Show |
1 | a0001c0001t0002g0047 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-109+1365_-109+136 others(38): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509947 | ||||||
chr19:15509954 | G | GTC | 141 | a0001c0001t0001g0003 a0001c0001t0001g0171 a0001c0001t0001g0173 others(138): Show |
143 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-109+1381_-109+138 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509954 | ||||||
chr19:15509962 | C | CTCTT | 3 | a0001c0001t0002g0311 a0001c0002t0003g0330 a0001c0002t0004g0331 |
3 | HG01891.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-109+1397_-109+140 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509962 | ||||||
chr19:15509962 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0021 others(6): Show |
9 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1379C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509962 | |||||||
chr19:15509988 | G | T | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1405G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509988 | |||||||
chr19:15510187 | G | T | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1604G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510187 | |||||||
chr19:15510197 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-109+1614G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510197 | |||||||
chr19:15510228 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(15): Show |
18 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.-109+1645C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510228 | |||||||
chr19:15510285 | C | T | 2 | a0002c0003t0002g0007 a0002c0003t0002g0008 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-109+1702C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510285 | |||||||
chr19:15510318 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-109+1735C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510318 | |||||||
chr19:15510369 | G | A | 325 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(322): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-109+1786G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510369 | |||||||
chr19:15510506 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-109+1923C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510506 | |||||||
chr19:15510507 | G | A | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1924G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510507 | |||||||
chr19:15510522 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0321 a0001c0001t0001g0326 others(78): Show |
82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.-109+1939A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510522 | |||||||
chr19:15510572 | T | C | 1 | a0002c0003t0002g0361 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-109+1989T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510572 | |||||||
chr19:15510575 | G | T | 8 | a0001c0001t0001g0215 a0001c0001t0002g0216 a0001c0001t0002g0217 others(5): Show |
8 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+1992G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510575 | |||||||
chr19:15510598 | A | G | 1 | a0001c0002t0002g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-109+2015A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510598 | |||||||
chr19:15510606 | A | T | 1 | a0001c0001t0004g0011 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-109+2023A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510606 | |||||||
chr19:15510637 | C | G | 2 | a0001c0002t0003g0010 a0005c0006t0005g0009 |
2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-109+2054C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510637 | |||||||
chr19:15510692 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(84): Show |
88 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.-109+2109T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510692 | |||||||
chr19:15510797 | AATTTAG | A | 7 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(4): Show |
7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+2216_-109+222 others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510797 | ||||||
chr19:15510935 | A | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(18): Show |
21 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+2352A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510935 | |||||||
chr19:15510945 | C | CAT | 26 | a0001c0001t0001g0153 a0001c0001t0001g0187 a0001c0001t0001g0188 others(23): Show |
26 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-109+2383_-109+238 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | ||||||
chr19:15510945 | C | CATAT | 10 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0110 others(7): Show |
10 | HG00673.hp1 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+2381_-109+238 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | ||||||
chr19:15510945 | C | CATATAT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0006g0001 |
3 | HG01257.hp2 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-109+2379_-109+238 others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | ||||||
chr19:15510945 | C | CATATATA others(3): Show |
1 | a0001c0001t0005g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-109+2375_-109+238 others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | ||||||
chr19:15510945 | CAT | C | 12 | a0001c0001t0001g0343 a0001c0001t0001g0360 a0001c0001t0002g0341 others(9): Show |
12 | HG00099.hp1 HG01081.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-109+2383_-109+238 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | ||||||
chr19:15510958 | A | T | 6 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0004g0011 others(3): Show |
6 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+2375A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510958 | |||||||
chr19:15510964 | A | AT | 4 | a0001c0001t0001g0275 a0001c0001t0002g0249 a0001c0001t0006g0271 others(1): Show |
4 | HG01167.hp2 NA18906.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+2382dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510964 | ||||||
chr19:15510964 | A | ATT | 9 | a0001c0001t0001g0215 a0001c0001t0001g0242 a0001c0001t0002g0197 others(6): Show |
9 | HG00609.hp2 HG02040.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+2382_-109+238 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510964 | ||||||
chr19:15510964 | A | T | 7 | a0001c0004t0001g0089 a0001c0004t0001g0091 a0001c0004t0001g0093 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+2381A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510964 | |||||||
chr19:15510966 | A | AT | 9 | a0001c0001t0001g0073 a0001c0001t0001g0165 a0001c0001t0001g0221 others(6): Show |
9 | HG01361.hp1 HG02040.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-109+2400dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATAT | 7 | a0001c0001t0001g0268 a0001c0001t0001g0286 a0001c0001t0002g0174 others(4): Show |
7 | HG00280.hp1 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0006 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(12): Show |
2 | a0001c0001t0004g0014 a0001c0001t0004g0017 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(36): Show |
1 | a0001c0001t0002g0023 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(47): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(32): Show |
1 | a0001c0001t0002g0022 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(43): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(25): Show |
1 | a0001c0002t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(28): Show |
1 | a0001c0001t0003g0027 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(39): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(26): Show |
1 | a0001c0001t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(37): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(12): Show |
2 | a0001c0001t0002g0015 a0001c0001t0004g0011 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(13): Show |
1 | a0001c0001t0004g0013 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(8): Show |
1 | a0001c0002t0003g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(7): Show |
1 | a0001c0001t0009g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATAT others(10): Show |
1 | a0004c0008t0001g0024 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATTT others(4): Show |
1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATATTT others(6): Show |
1 | a0001c0005t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATT | 11 | a0001c0001t0001g0222 a0001c0001t0001g0273 a0001c0001t0001g0274 others(8): Show |
11 | HG02080.hp2 HG04184.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATTTTT others(4): Show |
2 | a0002c0003t0002g0007 a0002c0003t0002g0008 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATATTTTT others(7): Show |
1 | a0010c0018t0002g0378 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATT | 59 | a0001c0001t0001g0003 a0001c0001t0001g0171 a0001c0001t0001g0173 others(56): Show |
60 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-109+2399_-109+240 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | ATTT | 6 | a0001c0001t0001g0234 a0001c0001t0001g0243 a0001c0001t0002g0004 others(3): Show |
7 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+2398_-109+240 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | A | T | 30 | a0001c0001t0001g0063 a0001c0001t0001g0215 a0001c0001t0001g0242 others(27): Show |
30 | HG00609.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.-109+2383A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510966 | |||||||
chr19:15510966 | AT | A | 19 | a0001c0001t0001g0026 a0001c0001t0001g0057 a0001c0001t0001g0177 others(16): Show |
20 | HG01515.hp1 HG02004.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-109+2400delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510966 | ATT | A | 31 | a0001c0001t0001g0321 a0001c0001t0001g0326 a0001c0001t0001g0335 others(28): Show |
31 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(28): Show |
intron_variant | MODIFIER | c.-109+2399_-109+240 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | ||||||
chr19:15510967 | T | TA | 7 | a0001c0001t0001g0115 a0001c0001t0001g0190 a0001c0001t0001g0191 others(4): Show |
7 | HG00642.hp2 HG01243.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510967 | |||||||
chr19:15510967 | T | TATATATA others(26): Show |
2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG01891.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(37): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510967 | |||||||
chr19:15510968 | T | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0037 others(89): Show |
93 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.-109+2385T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510968 | |||||||
chr19:15510969 | T | A | 5 | a0001c0001t0001g0057 a0001c0001t0002g0048 a0001c0001t0002g0290 others(2): Show |
5 | HG01515.hp1 HG02071.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+2386T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510969 | |||||||
chr19:15510970 | T | A | 24 | a0001c0001t0001g0033 a0001c0001t0001g0128 a0001c0001t0001g0159 others(21): Show |
24 | HG01070.hp1 HG01255.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.-109+2387T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510970 | |||||||
chr19:15510972 | T | A | 1 | a0001c0001t0001g0033 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-109+2389T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510972 | |||||||
chr19:15511028 | G | A | 1 | a0002c0003t0004g0098 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-109+2445G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511028 | |||||||
chr19:15511059 | C | T | 1 | a0001c0005t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+2476C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511059 | |||||||
chr19:15511062 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0177 |
3 | HG02004.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-109+2479G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511062 | |||||||
chr19:15511075 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-109+2492T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511075 | |||||||
chr19:15511183 | C | A | 8 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0021 others(5): Show |
8 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+2600C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511183 | |||||||
chr19:15511208 | C | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(145): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-109+2625C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511208 | |||||||
chr19:15511324 | T | C | 3 | a0001c0001t0001g0376 a0001c0001t0004g0375 a0002c0003t0001g0374 |
3 | HG02109.hp1 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-109+2741T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511324 | |||||||
chr19:15511331 | C | T | 1 | a0001c0001t0002g0279 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-109+2748C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511331 | |||||||
chr19:15511378 | A | G | 1 | a0001c0001t0004g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-109+2795A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511378 | |||||||
chr19:15511542 | T | G | 1 | a0001c0001t0003g0348 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-109+2959T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511542 | |||||||
chr19:15511693 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0056 others(6): Show |
9 | HG01257.hp2 HG01258.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.-109+3110G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511693 | |||||||
chr19:15511717 | C | T | 2 | a0001c0005t0004g0018 a0001c0005t0004g0019 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+3134C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511717 | |||||||
chr19:15511847 | C | T | 3 | a0001c0001t0004g0076 a0001c0001t0004g0077 a0001c0001t0015g0162 |
3 | HG02027.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-109+3264C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511847 | |||||||
chr19:15511908 | G | A | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-109+3325G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511908 | |||||||
chr19:15511954 | G | A | 1 | a0001c0001t0004g0372 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-109+3371G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511954 | |||||||
chr19:15512071 | TATCAAAT others(12): Show |
T | 1 | a0001c0001t0001g0062 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+3490_-109+350 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15512071 | ||||||
chr19:15512298 | C | T | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+3715C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512298 | |||||||
chr19:15512314 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(318): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-109+3731T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512314 | |||||||
chr19:15512324 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-109+3741A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512324 | |||||||
chr19:15512395 | G | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0171 a0001c0001t0001g0173 others(132): Show |
137 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-109+3812G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512395 | |||||||
chr19:15512719 | G | T | 1 | a0001c0001t0002g0290 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-109+4136G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512719 | |||||||
chr19:15512819 | A | G | 1 | a0001c0001t0002g0020 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-109+4236A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512819 | |||||||
chr19:15512829 | T | C | 6 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+4246T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512829 | |||||||
chr19:15512992 | T | TTC | 144 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(141): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-109+4429_-109+443 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15512992 | ||||||
chr19:15512992 | TTCTCTCT others(1): Show |
T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(18): Show |
21 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+4423_-109+443 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15512992 | ||||||
chr19:15513091 | G | A | 321 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(318): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-109+4508G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513091 | |||||||
chr19:15513129 | G | C | 3 | a0001c0001t0001g0173 a0001c0001t0001g0196 a0001c0001t0001g0234 |
3 | NA18967.hp1 NA19005.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-109+4546G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513129 | |||||||
chr19:15513240 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(173): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-109+4657T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513240 | |||||||
chr19:15513274 | C | G | 4 | a0001c0001t0002g0099 a0001c0001t0004g0107 a0001c0001t0004g0148 others(1): Show |
4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+4691C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513274 | |||||||
chr19:15513333 | G | T | 2 | a0001c0002t0003g0010 a0005c0006t0005g0009 |
2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-109+4750G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513333 | |||||||
chr19:15513349 | G | GTA | 74 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(71): Show |
75 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-109+4778_-109+477 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15513349 | ||||||
chr19:15513349 | G | GTATA | 17 | a0001c0001t0001g0067 a0001c0001t0001g0133 a0001c0001t0001g0142 others(14): Show |
18 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.-109+4776_-109+477 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15513349 | ||||||
chr19:15513361 | AT | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0099 others(14): Show |
17 | HG00733.hp2 HG01169.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.-109+4799delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15513361 | ||||||
chr19:15513362 | T | TA | 67 | a0001c0001t0001g0026 a0001c0001t0001g0171 a0001c0001t0001g0253 others(64): Show |
67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-109+4779_-109+478 others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513362 | |||||||
chr19:15513362 | T | TATA | 13 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0059 others(10): Show |
13 | HG01891.hp2 HG02132.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-109+4779_-109+478 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513362 | |||||||
chr19:15513363 | T | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0037 others(235): Show |
242 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-109+4780T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513363 | |||||||
chr19:15513364 | T | A | 81 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0059 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.-109+4781T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513364 | |||||||
chr19:15513365 | T | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0041 others(179): Show |
186 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.-109+4782T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513365 | |||||||
chr19:15513366 | T | A | 35 | a0001c0001t0001g0033 a0001c0001t0001g0246 a0001c0001t0001g0253 others(32): Show |
35 | HG00544.hp1 HG00558.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-109+4783T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513366 | |||||||
chr19:15513367 | T | A | 32 | a0001c0001t0001g0151 a0001c0001t0001g0173 a0001c0001t0001g0182 others(29): Show |
32 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-109+4784T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513367 | |||||||
chr19:15513368 | T | A | 8 | a0001c0001t0001g0253 a0001c0001t0001g0376 a0001c0001t0002g0099 others(5): Show |
8 | HG00544.hp1 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+4785T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513368 | |||||||
chr19:15513369 | T | A | 7 | a0001c0001t0001g0202 a0001c0001t0001g0219 a0001c0001t0001g0233 others(4): Show |
7 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+4786T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513369 | |||||||
chr19:15513371 | T | A | 1 | a0001c0001t0009g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+4788T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513371 | |||||||
chr19:15513384 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+4801A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513384 | |||||||
chr19:15513406 | C | T | 1 | a0006c0017t0002g0364 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-109+4823C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513406 | |||||||
chr19:15513407 | G | C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(18): Show |
21 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+4824G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513407 | |||||||
chr19:15513409 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+4826G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513409 | |||||||
chr19:15513457 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-109+4874C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513457 | |||||||
chr19:15513490 | G | A | 9 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(6): Show |
9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+4907G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513490 | |||||||
chr19:15513538 | T | G | 21 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(18): Show |
21 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+4955T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513538 | |||||||
chr19:15513540 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+4957A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513540 | |||||||
chr19:15513565 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0153 others(136): Show |
141 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.-109+4982C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513565 | |||||||
chr19:15513616 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-109+5033G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513616 | |||||||
chr19:15513743 | C | T | 4 | a0001c0001t0002g0125 a0001c0001t0004g0132 a0001c0001t0013g0131 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+5160C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513743 | |||||||
chr19:15513754 | C | T | 1 | a0001c0001t0003g0303 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-109+5171C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513754 | |||||||
chr19:15513768 | G | T | 1 | a0005c0006t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-109+5185G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513768 | |||||||
chr19:15513912 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-109+5329G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513912 | |||||||
chr19:15514074 | T | G | 1 | a0001c0001t0002g0036 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-109+5491T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514074 | |||||||
chr19:15514237 | T | G | 1 | a0001c0001t0001g0335 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-109+5654T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514237 | |||||||
chr19:15514361 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-109+5778T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514361 | |||||||
chr19:15514458 | C | T | 2 | a0001c0001t0001g0340 a0001c0001t0001g0358 |
2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-109+5875C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514458 | |||||||
chr19:15514469 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-109+5886C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514469 | |||||||
chr19:15514488 | C | T | 2 | a0002c0003t0002g0007 a0002c0003t0002g0008 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-109+5905C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514488 | |||||||
chr19:15514844 | C | T | 1 | a0001c0001t0002g0096 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-109+6261C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514844 | |||||||
chr19:15514930 | C | G | 1 | a0001c0001t0009g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+6347C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514930 | |||||||
chr19:15515298 | G | C | 1 | a0001c0001t0009g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+6715G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515298 | |||||||
chr19:15515315 | A | G | 1 | a0001c0001t0005g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-109+6732A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515315 | |||||||
chr19:15515423 | T | C | 1 | a0002c0003t0002g0361 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-109+6840T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515423 | |||||||
chr19:15515606 | A | C | 4 | a0001c0001t0002g0319 a0002c0003t0001g0317 a0002c0003t0003g0005 others(1): Show |
5 | HG02280.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+7023A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515606 | |||||||
chr19:15515705 | A | G | 24 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(21): Show |
24 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-109+7122A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515705 | |||||||
chr19:15515787 | G | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0153 others(133): Show |
138 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.-109+7204G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515787 | |||||||
chr19:15515792 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-109+7209C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515792 | |||||||
chr19:15515793 | G | A | 2 | a0001c0001t0004g0076 a0001c0001t0004g0077 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-109+7210G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515793 | |||||||
chr19:15515798 | A | G | 1 | a0001c0001t0003g0002 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-109+7215A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515798 | |||||||
chr19:15515872 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-109+7289C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515872 | |||||||
chr19:15515875 | C | T | 6 | a0001c0001t0001g0335 a0001c0001t0001g0371 a0001c0001t0002g0337 others(3): Show |
6 | HG01123.hp1 HG01516.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+7292C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515875 | |||||||
chr19:15515885 | G | T | 1 | a0001c0002t0003g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+7302G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515885 | |||||||
chr19:15515913 | T | C | 2 | a0001c0001t0002g0256 a0001c0002t0003g0028 |
2 | HG01175.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-109+7330T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515913 | |||||||
chr19:15516013 | G | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(17): Show |
20 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+7430G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516013 | |||||||
chr19:15516019 | G | A | 3 | a0001c0001t0002g0084 a0001c0001t0002g0096 a0001c0001t0002g0112 |
3 | HG00408.hp1 NA18959.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-109+7436G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516019 | |||||||
chr19:15516047 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-109+7464A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516047 | |||||||
chr19:15516135 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-109+7552G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516135 | |||||||
chr19:15516218 | C | T | 2 | a0001c0001t0009g0012 a0001c0005t0002g0016 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-108-7475C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516218 | |||||||
chr19:15516280 | C | T | 2 | a0001c0001t0009g0012 a0001c0005t0002g0016 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-108-7413C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516280 | |||||||
chr19:15516351 | C | T | 3 | a0001c0001t0002g0174 a0001c0001t0003g0181 a0001c0001t0003g0291 |
3 | NA18990.hp2 NA18999.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-108-7342C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516351 | |||||||
chr19:15516397 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(319): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-108-7296A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516397 | |||||||
chr19:15516491 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0006g0180 |
2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-108-7202C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516491 | |||||||
chr19:15516674 | G | A | 1 | a0001c0001t0003g0113 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-108-7019G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516674 | |||||||
chr19:15516814 | G | A | 1 | a0001c0001t0002g0004 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-108-6879G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516814 | |||||||
chr19:15516835 | C | CT | 141 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0062 others(138): Show |
143 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-108-6839dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15516835 | ||||||
chr19:15516835 | CT | C | 6 | a0001c0001t0002g0036 a0001c0001t0004g0076 a0001c0001t0004g0077 others(3): Show |
6 | HG02071.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-6839delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15516835 | ||||||
chr19:15516858 | A | G | 1 | a0001c0001t0002g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-108-6835A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516858 | |||||||
chr19:15516859 | C | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0153 others(154): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-108-6834C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516859 | |||||||
chr19:15516950 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0004g0011 others(3): Show |
6 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-6743C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516950 | |||||||
chr19:15517012 | G | A | 48 | a0001c0001t0001g0321 a0001c0001t0001g0326 a0001c0001t0001g0333 others(45): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.-108-6681G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517012 | |||||||
chr19:15517019 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-108-6674C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517019 | |||||||
chr19:15517064 | G | A | 1 | a0002c0003t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-108-6629G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517064 | |||||||
chr19:15517103 | G | T | 1 | a0005c0006t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-108-6590G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517103 | |||||||
chr19:15517116 | C | T | 2 | a0002c0003t0002g0218 a0006c0016t0005g0109 |
2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-6577C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517116 | |||||||
chr19:15517161 | A | AT | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(176): Show |
181 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.-108-6523dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15517161 | ||||||
chr19:15517245 | A | G | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-108-6448A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517245 | |||||||
chr19:15517250 | C | A | 9 | a0001c0004t0001g0089 a0001c0004t0001g0091 a0001c0004t0001g0093 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-6443C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517250 | |||||||
chr19:15517260 | T | C | 3 | a0001c0001t0002g0174 a0001c0001t0003g0181 a0001c0001t0003g0291 |
3 | NA18990.hp2 NA18999.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-108-6433T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517260 | |||||||
chr19:15517276 | A | T | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-6417A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517276 | |||||||
chr19:15517402 | C | T | 1 | a0001c0001t0004g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-108-6291C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517402 | |||||||
chr19:15517638 | G | A | 8 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0021 others(5): Show |
8 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-6055G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517638 | |||||||
chr19:15517641 | T | C | 1 | a0001c0002t0002g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-108-6052T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517641 | |||||||
chr19:15517908 | C | T | 1 | a0002c0003t0002g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-108-5785C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517908 | |||||||
chr19:15517974 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(134): Show |
139 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.-108-5719G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517974 | |||||||
chr19:15518156 | GCCAGACC others(9): Show |
G | 2 | a0001c0001t0001g0037 a0001c0001t0001g0064 |
2 | NA18943.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.-108-5533_-108-551 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518156 | ||||||
chr19:15518484 | C | CA | 264 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0033 others(261): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.-108-5194dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518484 | ||||||
chr19:15518484 | C | CAA | 19 | a0001c0001t0001g0029 a0001c0001t0001g0059 a0001c0001t0001g0073 others(16): Show |
19 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-5195_-108-519 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518484 | ||||||
chr19:15518496 | A | ATAT | 9 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(6): Show |
9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-5197_-108-519 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518496 | |||||||
chr19:15518498 | A | AAAT | 9 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0021 others(6): Show |
9 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-5194_-108-519 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518498 | ||||||
chr19:15518498 | A | ATAT | 8 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0004g0011 others(5): Show |
8 | HG02622.hp1 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108-5195_-108-519 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518498 | |||||||
chr19:15518498 | A | T | 9 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(6): Show |
9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-5195A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518498 | |||||||
chr19:15518603 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0376 a0001c0001t0002g0015 others(14): Show |
17 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.-108-5090C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518603 | |||||||
chr19:15518647 | C | CA | 45 | a0001c0001t0001g0062 a0001c0001t0001g0128 a0001c0001t0001g0165 others(42): Show |
46 | HG00621.hp1 HG00741.hp1 HG01358.hp1 others(43): Show |
intron_variant | MODIFIER | c.-108-5024dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | ||||||
chr19:15518647 | C | CAA | 12 | a0001c0001t0002g0053 a0001c0001t0002g0106 a0001c0001t0003g0300 others(9): Show |
12 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108-5025_-108-502 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | ||||||
chr19:15518647 | C | CAAA | 8 | a0001c0004t0001g0091 a0001c0004t0001g0093 a0001c0004t0001g0116 others(5): Show |
8 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-5026_-108-502 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | ||||||
chr19:15518647 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-108-5046C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518647 | |||||||
chr19:15518647 | CA | C | 10 | a0001c0001t0001g0044 a0001c0001t0002g0015 a0001c0001t0002g0099 others(7): Show |
10 | HG01099.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-5024delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | ||||||
chr19:15518647 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-108-5033_-108-502 others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | ||||||
chr19:15518688 | GA | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0165 others(33): Show |
36 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-108-4991delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518688 | ||||||
chr19:15518698 | A | G | 4 | a0001c0001t0002g0099 a0001c0001t0004g0107 a0001c0001t0004g0148 others(1): Show |
4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-4995A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518698 | |||||||
chr19:15518718 | CAA | C | 8 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0021 others(5): Show |
8 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-4972_-108-497 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518718 | ||||||
chr19:15518782 | G | T | 1 | a0001c0001t0002g0266 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-108-4911G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518782 | |||||||
chr19:15518858 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(324): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.-108-4835T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518858 | |||||||
chr19:15519008 | G | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0002g0015 others(29): Show |
32 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108-4685G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519008 | |||||||
chr19:15519019 | G | C | 7 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(4): Show |
7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-4674G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519019 | |||||||
chr19:15519141 | C | T | 1 | a0002c0003t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-108-4552C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519141 | |||||||
chr19:15519172 | C | T | 4 | a0001c0001t0002g0099 a0001c0001t0004g0107 a0001c0001t0004g0148 others(1): Show |
4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-4521C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519172 | |||||||
chr19:15519181 | G | C | 3 | a0001c0001t0001g0365 a0001c0001t0003g0366 a0001c0001t0003g0368 |
3 | HG00099.hp2 HG01069.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-108-4512G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519181 | |||||||
chr19:15519211 | A | G | 2 | a0001c0001t0009g0012 a0001c0005t0002g0016 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-108-4482A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519211 | |||||||
chr19:15519262 | G | GA | 3 | a0001c0001t0001g0062 a0001c0001t0002g0137 a0001c0001t0006g0156 |
3 | HG02080.hp1 NA18991.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-108-4430dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15519262 | ||||||
chr19:15519263 | A | AT | 17 | a0001c0001t0001g0080 a0001c0001t0001g0115 a0001c0001t0001g0165 others(14): Show |
17 | HG01109.hp1 HG01192.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-108-4413dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15519263 | ||||||
chr19:15519264 | T | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-108-4429T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519264 | |||||||
chr19:15519302 | A | G | 330 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(327): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-108-4391A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519302 | |||||||
chr19:15519407 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(140): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.-108-4286C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519407 | |||||||
chr19:15519465 | G | T | 2 | a0001c0001t0002g0095 a0001c0001t0003g0179 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-108-4228G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519465 | |||||||
chr19:15519475 | C | G | 1 | a0001c0001t0002g0121 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-108-4218C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519475 | |||||||
chr19:15519493 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0002g0021 others(6): Show |
9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-4200C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519493 | |||||||
chr19:15519578 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(139): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-108-4115T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519578 | |||||||
chr19:15519642 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(130): Show |
135 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.-108-4051G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519642 | |||||||
chr19:15519787 | A | G | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-108-3906A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519787 | |||||||
chr19:15519864 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-108-3829C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519864 | |||||||
chr19:15519872 | T | C | 3 | a0001c0001t0004g0192 a0001c0001t0009g0012 a0001c0005t0002g0016 |
3 | HG02257.hp1 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-108-3821T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519872 | |||||||
chr19:15520071 | G | T | 2 | a0001c0001t0004g0076 a0001c0001t0004g0077 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-108-3622G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520071 | |||||||
chr19:15520115 | C | T | 1 | a0001c0001t0002g0323 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-108-3578C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520115 | |||||||
chr19:15520218 | C | T | 2 | a0001c0001t0001g0221 a0001c0001t0001g0239 |
2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-108-3475C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520218 | |||||||
chr19:15520219 | G | A | 10 | a0001c0001t0001g0151 a0001c0001t0002g0051 a0001c0001t0002g0053 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-3474G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520219 | |||||||
chr19:15520310 | T | C | 1 | a0001c0012t0002g0203 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-108-3383T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520310 | |||||||
chr19:15520325 | G | A | 1 | a0001c0012t0002g0203 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-108-3368G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520325 | |||||||
chr19:15520327 | C | T | 1 | a0001c0012t0002g0203 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-108-3366C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520327 | |||||||
chr19:15520336 | C | A | 1 | a0001c0012t0002g0203 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-108-3357C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520336 | |||||||
chr19:15520345 | C | CA | 71 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0062 others(68): Show |
71 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-108-3332dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520345 | ||||||
chr19:15520356 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-108-3337A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520356 | |||||||
chr19:15520362 | C | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(150): Show |
155 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.-108-3331C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520362 | |||||||
chr19:15520402 | G | GT | 138 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(135): Show |
140 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.-108-3280dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520402 | ||||||
chr19:15520402 | G | GTT | 7 | a0001c0001t0001g0274 a0001c0001t0001g0282 a0001c0001t0001g0283 others(4): Show |
7 | HG02074.hp1 NA18945.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-3281_-108-328 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520402 | ||||||
chr19:15520552 | G | A | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-108-3141G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520552 | |||||||
chr19:15520681 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0002g0021 others(6): Show |
9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-3012A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520681 | |||||||
chr19:15520687 | A | G | 1 | a0001c0001t0002g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-108-3006A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520687 | |||||||
chr19:15520719 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-108-2974C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520719 | |||||||
chr19:15520727 | A | G | 15 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(12): Show |
15 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-2966A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520727 | |||||||
chr19:15520761 | G | GT | 5 | a0001c0001t0001g0043 a0001c0001t0002g0252 a0001c0001t0004g0076 others(2): Show |
5 | HG02074.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-2928dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520761 | ||||||
chr19:15520763 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-108-2930T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520763 | |||||||
chr19:15520766 | G | T | 135 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(132): Show |
137 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-108-2927G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520766 | |||||||
chr19:15520774 | G | GT | 12 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0114 others(9): Show |
12 | HG00621.hp1 HG00741.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108-2907dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520774 | ||||||
chr19:15520774 | GT | G | 17 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(14): Show |
17 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-108-2907delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520774 | ||||||
chr19:15520957 | C | T | 2 | a0002c0003t0002g0007 a0002c0003t0002g0008 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-108-2736C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520957 | |||||||
chr19:15521052 | C | T | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-2641C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521052 | |||||||
chr19:15521231 | C | CT | 23 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0001g0115 others(20): Show |
23 | HG00621.hp2 HG00741.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.-108-2444dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15521231 | ||||||
chr19:15521231 | CT | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(164): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.-108-2444delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15521231 | ||||||
chr19:15521262 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(139): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-108-2431C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521262 | |||||||
chr19:15521421 | C | T | 2 | a0001c0001t0009g0012 a0001c0005t0002g0016 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-108-2272C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521421 | |||||||
chr19:15521524 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0002g0021 others(6): Show |
9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-2169G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521524 | |||||||
chr19:15521755 | C | T | 1 | a0001c0001t0005g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-108-1938C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521755 | |||||||
chr19:15521824 | C | G | 6 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0004g0011 others(3): Show |
6 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-1869C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521824 | |||||||
chr19:15521834 | C | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(126): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.-108-1859C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521834 | |||||||
chr19:15521878 | C | T | 1 | a0004c0008t0004g0377 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-108-1815C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521878 | |||||||
chr19:15521882 | C | T | 10 | a0001c0001t0001g0151 a0001c0001t0002g0051 a0001c0001t0002g0053 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-1811C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521882 | |||||||
chr19:15521942 | C | T | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-1751C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521942 | |||||||
chr19:15521961 | A | G | 10 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-1732A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521961 | |||||||
chr19:15522022 | A | G | 4 | a0001c0001t0002g0099 a0001c0001t0004g0107 a0001c0001t0004g0148 others(1): Show |
4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-1671A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522022 | |||||||
chr19:15522147 | GA | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(128): Show |
133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.-108-1527delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15522147 | ||||||
chr19:15522573 | G | A | 1 | a0001c0001t0005g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-108-1120G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522573 | |||||||
chr19:15522625 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(137): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-108-1068G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522625 | |||||||
chr19:15522666 | G | A | 8 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(5): Show |
8 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108-1027G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522666 | |||||||
chr19:15522724 | G | T | 2 | a0001c0001t0001g0159 a0001c0001t0002g0176 |
2 | NA18977.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-108-969G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522724 | |||||||
chr19:15522734 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-108-959G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522734 | |||||||
chr19:15522745 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-108-948C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522745 | |||||||
chr19:15522773 | C | T | 15 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(12): Show |
15 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-920C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522773 | |||||||
chr19:15522872 | G | A | 1 | a0001c0002t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-108-821G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522872 | |||||||
chr19:15522934 | C | T | 1 | a0006c0017t0002g0364 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-108-759C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522934 | |||||||
chr19:15522962 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-108-731C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522962 | |||||||
chr19:15523130 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-108-563G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523130 | |||||||
chr19:15523314 | C | T | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-379C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523314 | |||||||
chr19:15523534 | G | A | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-159G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523534 | |||||||
chr19:15523653 | A | G | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-40A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523653 | |||||||
chr19:15523654 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(5): Show |
8 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108-39A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523654 | |||||||
chr19:15523671 | C | A | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-22C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523671 | |||||||
chr19:15524064 | G | GA | 134 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(131): Show |
136 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.-2+279dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524064 | ||||||
chr19:15524064 | GA | G | 8 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(5): Show |
8 | HG00621.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+279delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524064 | ||||||
chr19:15524208 | G | T | 2 | a0001c0005t0004g0018 a0001c0005t0004g0019 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-2+409G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524208 | |||||||
chr19:15524372 | G | A | 2 | a0001c0001t0002g0051 a0001c0001t0003g0050 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-2+573G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524372 | |||||||
chr19:15524409 | G | A | 2 | a0001c0001t0009g0012 a0001c0005t0002g0016 |
2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-2+610G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524409 | |||||||
chr19:15524640 | C | A | 1 | a0001c0001t0002g0379 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-696C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524640 | |||||||
chr19:15524669 | G | GGA | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-654_-1-653dupGA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524669 | ||||||
chr19:15524680 | G | GAGAA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0029 others(144): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-1-636_-1-633dupAA others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524680 | ||||||
chr19:15524680 | GAGAA | G | 10 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0002g0021 others(7): Show |
10 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-636_-1-633delAA others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524680 | ||||||
chr19:15524700 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0002g0021 others(6): Show |
9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-636A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524700 | |||||||
chr19:15524708 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0002g0021 others(6): Show |
9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-628G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524708 | |||||||
chr19:15525148 | C | T | 2 | a0001c0001t0004g0076 a0001c0001t0004g0077 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-1-188C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15525148 | |||||||
chr19:15525283 | A | G | 4 | a0001c0001t0002g0099 a0001c0001t0004g0107 a0001c0001t0004g0148 others(1): Show |
4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-53A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15525283 | |||||||
chr19:15525307 | A | G | 13 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(10): Show |
13 | HG02109.hp1 HG02109.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1-29A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15525307 | |||||||
chr19:15525310 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-1-26G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15525310 | |||||||
chr19:15525626 | T | C | 7 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(4): Show |
7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+68T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15525626 | |||||||
chr19:15525694 | G | C | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.222+136G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15525694 | |||||||
chr19:15525871 | T | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(173): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.222+313T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15525871 | |||||||
chr19:15525959 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0195 a0001c0001t0003g0199 |
3 | NA18950.hp2 NA18957.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.222+401C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15525959 | |||||||
chr19:15526127 | C | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(126): Show |
131 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.222+569C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526127 | |||||||
chr19:15526240 | T | A | 5 | a0001c0001t0001g0033 a0001c0001t0002g0030 a0001c0001t0002g0034 others(2): Show |
5 | NA18612.hp1 NA18946.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+682T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526240 | |||||||
chr19:15526295 | T | C | 7 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(4): Show |
7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+737T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526295 | |||||||
chr19:15526347 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0002g0087 |
2 | HG02083.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.222+789C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526347 | |||||||
chr19:15526520 | C | A | 8 | a0001c0001t0001g0151 a0001c0001t0002g0051 a0001c0001t0002g0053 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+962C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526520 | |||||||
chr19:15526565 | GC | G | 8 | a0001c0001t0001g0151 a0001c0001t0002g0051 a0001c0001t0002g0053 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+1008delC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526565 | |||||||
chr19:15526747 | C | CT | 10 | a0001c0001t0001g0234 a0001c0001t0001g0376 a0001c0001t0002g0379 others(7): Show |
10 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+1205dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15526747 | ||||||
chr19:15526765 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.222+1207G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526765 | |||||||
chr19:15526783 | T | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0376 others(25): Show |
28 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.222+1225T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526783 | |||||||
chr19:15526906 | C | T | 9 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(6): Show |
9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+1348C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526906 | |||||||
chr19:15527008 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.222+1450C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527008 | |||||||
chr19:15527111 | C | T | 1 | a0001c0001t0008g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.222+1553C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527111 | |||||||
chr19:15527195 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0002g0021 others(6): Show |
9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+1637G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527195 | |||||||
chr19:15527218 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.222+1660G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527218 | |||||||
chr19:15527266 | G | A | 1 | a0009c0019t0001g0146 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.222+1708G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527266 | |||||||
chr19:15527327 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.222+1769T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527327 | |||||||
chr19:15527331 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.222+1773C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527331 | |||||||
chr19:15527454 | A | G | 1 | a0001c0001t0002g0262 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.222+1896A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527454 | |||||||
chr19:15527676 | A | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0376 others(25): Show |
28 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.223-2033A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527676 | |||||||
chr19:15527689 | C | T | 19 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0074 others(16): Show |
19 | HG00408.hp2 HG00673.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.223-2020C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527689 | |||||||
chr19:15527726 | G | T | 9 | a0001c0001t0001g0006 a0001c0001t0002g0015 a0001c0001t0002g0021 others(6): Show |
9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-1983G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527726 | |||||||
chr19:15527747 | T | A | 7 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(4): Show |
7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-1962T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527747 | |||||||
chr19:15527863 | C | T | 1 | a0001c0001t0004g0132 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223-1846C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527863 | |||||||
chr19:15527951 | C | A | 1 | a0001c0001t0002g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.223-1758C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527951 | |||||||
chr19:15528172 | GCTGGGCA others(8): Show |
G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA18948.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.223-1535_223-1521d others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15528172 | ||||||
chr19:15528207 | C | T | 8 | a0001c0001t0001g0151 a0001c0001t0002g0051 a0001c0001t0002g0053 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-1502C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528207 | |||||||
chr19:15528263 | G | A | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.223-1446G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528263 | |||||||
chr19:15528422 | T | C | 1 | a0001c0002t0002g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223-1287T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528422 | |||||||
chr19:15528457 | T | C | 1 | a0001c0001t0002g0305 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.223-1252T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528457 | |||||||
chr19:15528484 | A | G | 8 | a0001c0001t0001g0151 a0001c0001t0002g0051 a0001c0001t0002g0053 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-1225A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528484 | |||||||
chr19:15528530 | T | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(137): Show |
142 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.223-1179T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528530 | |||||||
chr19:15528569 | GTCT | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.223-1134_223-1132d others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15528569 | ||||||
chr19:15528788 | A | T | 1 | a0001c0002t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.223-921A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528788 | |||||||
chr19:15528904 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.223-805A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528904 | |||||||
chr19:15528930 | T | C | 1 | a0001c0002t0002g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223-779T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528930 | |||||||
chr19:15529117 | C | T | 1 | a0002c0003t0002g0361 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.223-592C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529117 | |||||||
chr19:15529133 | A | AT | 26 | a0001c0001t0001g0376 a0001c0001t0002g0051 a0001c0001t0002g0053 others(23): Show |
26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.223-564dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15529133 | ||||||
chr19:15529133 | A | ATT | 160 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0026 others(157): Show |
162 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.223-565_223-564dup others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15529133 | ||||||
chr19:15529133 | A | ATTT | 7 | a0001c0001t0001g0237 a0001c0001t0003g0300 a0001c0001t0003g0301 others(4): Show |
7 | HG00621.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-566_223-564dup others(3): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15529133 | ||||||
chr19:15529136 | T | TTA | 141 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(138): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.223-572_223-571ins others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15529136 | ||||||
chr19:15529185 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0044 others(138): Show |
143 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.223-524A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529185 | |||||||
chr19:15529197 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.223-512C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529197 | |||||||
chr19:15529349 | G | A | 2 | a0002c0003t0002g0007 a0002c0003t0002g0008 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.223-360G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529349 | |||||||
chr19:15529477 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.223-232G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529477 | |||||||
chr19:15529596 | C | T | 1 | a0012c0014t0011g0288 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.223-113C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529596 | |||||||
chr19:15529858 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0002g0020 a0001c0001t0002g0022 others(4): Show |
7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.367+5G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15529858 | |||||||
chr19:15530161 | G | A | 183 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(180): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.367+308G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530161 | |||||||
chr19:15530167 | C | T | 1 | a0011c0015t0004g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.367+314C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530167 | |||||||
chr19:15530219 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0033 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.367+366C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530219 | |||||||
chr19:15530314 | C | T | 1 | a0001c0001t0009g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.367+461C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530314 | |||||||
chr19:15530384 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(289): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.367+531C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530384 | |||||||
chr19:15530386 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.367+533C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530386 | |||||||
chr19:15530531 | T | C | 1 | a0001c0001t0001g0243 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.367+678T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530531 | |||||||
chr19:15530578 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.367+725T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530578 | |||||||
chr19:15530643 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0006g0156 |
2 | NA18945.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.367+790C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530643 | |||||||
chr19:15530653 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.367+800G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530653 | |||||||
chr19:15530705 | C | A | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.367+852C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530705 | |||||||
chr19:15530938 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0006g0001 |
3 | HG01257.hp2 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.367+1085A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530938 | |||||||
chr19:15531025 | T | C | 1 | a0002c0003t0005g0327 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.367+1172T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531025 | |||||||
chr19:15531126 | C | T | 3 | a0001c0001t0001g0273 a0001c0001t0001g0275 a0001c0001t0001g0349 |
3 | HG00673.hp2 HG02080.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.367+1273C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531126 | |||||||
chr19:15531202 | C | T | 19 | a0001c0001t0001g0128 a0001c0001t0001g0135 a0001c0001t0001g0136 others(16): Show |
20 | HG00639.hp2 HG00642.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.367+1349C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531202 | |||||||
chr19:15531206 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.367+1353A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531206 | |||||||
chr19:15531283 | G | C | 1 | a0005c0006t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.367+1430G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531283 | |||||||
chr19:15531308 | A | C | 2 | a0001c0001t0001g0003 a0001c0001t0002g0211 |
3 | NA18948.hp2 NA19010.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.367+1455A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531308 | |||||||
chr19:15531321 | A | T | 1 | a0001c0002t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.367+1468A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531321 | |||||||
chr19:15531378 | G | T | 5 | a0001c0001t0001g0340 a0001c0001t0001g0357 a0001c0001t0001g0358 others(2): Show |
5 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.367+1525G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531378 | |||||||
chr19:15531384 | T | TA | 72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(69): Show |
72 | HG00408.hp2 HG00673.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.367+1546dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15531384 | ||||||
chr19:15531384 | T | TAA | 224 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0043 others(221): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.367+1545_367+1546d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15531384 | ||||||
chr19:15531384 | T | TAAA | 38 | a0001c0001t0001g0128 a0001c0001t0001g0135 a0001c0001t0001g0136 others(35): Show |
39 | HG00639.hp2 HG00642.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.367+1544_367+1546d others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15531384 | ||||||
chr19:15531433 | C | T | 1 | a0001c0001t0002g0095 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.367+1580C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531433 | |||||||
chr19:15531455 | G | A | 2 | a0001c0001t0003g0167 a0001c0005t0002g0016 |
2 | HG01175.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.367+1602G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531455 | |||||||
chr19:15531483 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.367+1630A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531483 | |||||||
chr19:15531663 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.367+1810A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531663 | |||||||
chr19:15531764 | G | A | 4 | a0001c0001t0002g0099 a0001c0001t0004g0107 a0001c0001t0004g0148 others(1): Show |
4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+1911G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531764 | |||||||
chr19:15532114 | T | TA | 14 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0151 others(11): Show |
14 | HG01934.hp1 HG01934.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.367+2271dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15532114 | ||||||
chr19:15532463 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.367+2610C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532463 | |||||||
chr19:15532497 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0135 others(36): Show |
40 | HG00639.hp2 HG00642.hp2 HG01934.hp2 others(37): Show |
intron_variant | MODIFIER | c.367+2644C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532497 | |||||||
chr19:15532549 | AT | A | 19 | a0001c0001t0001g0128 a0001c0001t0001g0135 a0001c0001t0001g0136 others(16): Show |
20 | HG00639.hp2 HG00642.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.367+2707delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15532549 | ||||||
chr19:15532571 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0003g0179 |
2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.367+2718G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532571 | |||||||
chr19:15532679 | GTC | G | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+2832_367+2833d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15532679 | ||||||
chr19:15532714 | C | T | 4 | a0001c0001t0003g0295 a0001c0001t0003g0297 a0001c0001t0003g0298 others(1): Show |
4 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+2861C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532714 | |||||||
chr19:15532718 | C | G | 9 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(6): Show |
9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+2865C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532718 | |||||||
chr19:15532779 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0056 others(122): Show |
126 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.367+2926G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532779 | |||||||
chr19:15532780 | A | C | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.367+2927A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532780 | |||||||
chr19:15532859 | A | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0135 others(46): Show |
50 | HG00639.hp2 HG00642.hp2 HG01934.hp2 others(47): Show |
intron_variant | MODIFIER | c.367+3006A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532859 | |||||||
chr19:15532869 | C | T | 40 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0135 others(37): Show |
41 | HG00639.hp2 HG00642.hp2 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.367+3016C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532869 | |||||||
chr19:15533043 | G | A | 22 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0002g0015 others(19): Show |
22 | HG01934.hp2 HG02257.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.367+3190G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533043 | |||||||
chr19:15533187 | A | G | 1 | a0001c0001t0004g0370 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.367+3334A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533187 | |||||||
chr19:15533372 | TA | T | 9 | a0001c0004t0001g0089 a0001c0004t0001g0091 a0001c0004t0001g0093 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+3526delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533372 | ||||||
chr19:15533379 | A | T | 9 | a0001c0004t0001g0089 a0001c0004t0001g0091 a0001c0004t0001g0093 others(6): Show |
9 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+3526A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533379 | |||||||
chr19:15533428 | C | T | 1 | a0001c0001t0004g0356 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.367+3575C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533428 | |||||||
chr19:15533591 | C | CT | 113 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0029 others(110): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.368-3748dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533591 | ||||||
chr19:15533591 | C | CTT | 23 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0367 others(20): Show |
24 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.368-3749_368-3748d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533591 | ||||||
chr19:15533591 | C | CTTT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0128 a0001c0001t0001g0151 others(10): Show |
13 | HG00642.hp2 HG01978.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.368-3750_368-3748d others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533591 | ||||||
chr19:15533591 | CT | C | 6 | a0001c0001t0001g0196 a0001c0001t0002g0047 a0001c0001t0002g0085 others(3): Show |
6 | HG01168.hp1 HG02897.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-3748delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533591 | ||||||
chr19:15533618 | C | T | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368-3743C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533618 | |||||||
chr19:15533622 | G | T | 1 | a0001c0001t0003g0027 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.368-3739G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533622 | |||||||
chr19:15533648 | A | G | 4 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(1): Show |
4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-3713A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533648 | |||||||
chr19:15533725 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.368-3636C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533725 | |||||||
chr19:15534018 | G | A | 6 | a0001c0001t0009g0012 a0001c0002t0003g0010 a0001c0005t0002g0016 others(3): Show |
6 | HG02257.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-3343G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534018 | |||||||
chr19:15534045 | G | A | 2 | a0001c0001t0002g0095 a0001c0001t0002g0296 |
2 | HG01358.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.368-3316G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534045 | |||||||
chr19:15534128 | T | C | 11 | a0001c0001t0001g0128 a0001c0001t0001g0135 a0001c0001t0001g0136 others(8): Show |
12 | HG00639.hp2 HG00642.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-3233T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534128 | |||||||
chr19:15534250 | T | C | 2 | a0001c0001t0002g0305 a0001c0001t0002g0306 |
2 | NA19064.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.368-3111T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534250 | |||||||
chr19:15534454 | A | G | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368-2907A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534454 | |||||||
chr19:15534605 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0041 others(201): Show |
206 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(203): Show |
intron_variant | MODIFIER | c.368-2756T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534605 | |||||||
chr19:15534656 | G | A | 329 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(326): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.368-2705G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534656 | |||||||
chr19:15534809 | C | T | 334 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(331): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.368-2552C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534809 | |||||||
chr19:15534958 | G | A | 10 | a0001c0004t0001g0089 a0001c0004t0001g0091 a0001c0004t0001g0093 others(7): Show |
10 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.368-2403G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534958 | |||||||
chr19:15535045 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.368-2316C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535045 | |||||||
chr19:15535098 | G | T | 1 | a0001c0005t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.368-2263G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535098 | |||||||
chr19:15535154 | A | G | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368-2207A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535154 | |||||||
chr19:15535213 | A | T | 2 | a0001c0001t0001g0309 a0001c0001t0003g0308 |
2 | NA18980.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.368-2148A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535213 | |||||||
chr19:15535240 | G | A | 19 | a0001c0001t0001g0128 a0001c0001t0001g0135 a0001c0001t0001g0136 others(16): Show |
20 | HG00639.hp2 HG00642.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.368-2121G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535240 | |||||||
chr19:15535384 | A | T | 1 | a0001c0002t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.368-1977A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535384 | |||||||
chr19:15535434 | G | T | 339 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(336): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.368-1927G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535434 | |||||||
chr19:15535557 | T | C | 1 | a0001c0001t0002g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.368-1804T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535557 | |||||||
chr19:15535671 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(158): Show |
162 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(159): Show |
intron_variant | MODIFIER | c.368-1690T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535671 | |||||||
chr19:15535860 | G | A | 2 | a0001c0001t0004g0231 a0001c0001t0004g0232 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.368-1501G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535860 | |||||||
chr19:15536041 | A | C | 1 | a0001c0002t0003g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.368-1320A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536041 | |||||||
chr19:15536159 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0029 others(46): Show |
50 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.368-1202C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536159 | |||||||
chr19:15536361 | A | C | 6 | a0001c0001t0002g0106 a0001c0001t0002g0323 a0001c0001t0004g0075 others(3): Show |
6 | HG01934.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-1000A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536361 | |||||||
chr19:15536381 | C | T | 52 | a0001c0001t0001g0210 a0001c0001t0001g0221 a0001c0001t0001g0250 others(49): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.368-980C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536381 | |||||||
chr19:15536391 | G | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0042 others(159): Show |
163 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.368-970G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536391 | |||||||
chr19:15536483 | G | C | 13 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0303 others(10): Show |
13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.368-878G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536483 | |||||||
chr19:15536500 | C | T | 1 | a0001c0001t0004g0370 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.368-861C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536500 | |||||||
chr19:15536559 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0004g0075 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.368-802G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536559 | |||||||
chr19:15536578 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.368-783G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536578 | |||||||
chr19:15536824 | T | G | 1 | a0001c0001t0002g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.368-537T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536824 | |||||||
chr19:15536831 | A | G | 11 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(8): Show |
11 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.368-530A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536831 | |||||||
chr19:15536848 | T | G | 2 | a0001c0005t0004g0018 a0001c0005t0004g0019 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.368-513T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536848 | |||||||
chr19:15536968 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.368-393G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536968 | |||||||
chr19:15537035 | G | A | 10 | a0001c0001t0007g0316 a0002c0003t0001g0317 a0002c0003t0002g0361 others(7): Show |
11 | HG02280.hp1 HG02451.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-326G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537035 | |||||||
chr19:15537072 | G | A | 41 | a0001c0001t0001g0128 a0001c0001t0001g0210 a0001c0001t0001g0250 others(38): Show |
41 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.368-289G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537072 | |||||||
chr19:15537144 | C | G | 1 | a0001c0001t0004g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.368-217C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537144 | |||||||
chr19:15537162 | A | G | 2 | a0001c0001t0002g0099 a0001c0001t0004g0107 |
2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.368-199A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537162 | |||||||
chr19:15537176 | C | T | 1 | a0001c0001t0005g0185 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.368-185C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537176 | |||||||
chr19:15537185 | C | T | 77 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0033 others(74): Show |
77 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.368-176C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537185 | |||||||
chr19:15537279 | T | C | 2 | a0001c0001t0009g0012 a0001c0004t0002g0178 |
2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.368-82T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537279 | |||||||
chr19:15537314 | C | A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0002g0015 others(5): Show |
8 | HG02559.hp1 HG02622.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.368-47C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537314 | |||||||
chr19:15537337 | C | T | 148 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0042 others(145): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.368-24C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537337 | |||||||
chr19:15537352 | C | G | 7 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0002g0015 others(4): Show |
7 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-9C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537352 | |||||||
chr19:15537490 | T | A | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.422-45T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 5/13 | chr19 | 15537490 | |||||||
chr19:15537807 | G | T | 1 | a0001c0001t0003g0278 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.550-65G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 6/13 | chr19 | 15537807 | |||||||
chr19:15538056 | G | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0001g0191 others(23): Show |
27 | HG00621.hp2 HG00639.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+63G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538056 | |||||||
chr19:15538158 | T | C | 6 | a0001c0001t0001g0153 a0001c0001t0001g0196 a0001c0001t0001g0234 others(3): Show |
6 | HG00735.hp2 HG02004.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.671+165T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538158 | |||||||
chr19:15538192 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.671+199C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538192 | |||||||
chr19:15538336 | G | A | 2 | a0001c0001t0003g0167 a0001c0001t0003g0352 |
2 | HG01167.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.671+343G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538336 | |||||||
chr19:15538392 | A | T | 7 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.671+399A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538392 | |||||||
chr19:15538473 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.671+480A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538473 | |||||||
chr19:15538482 | G | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.671+489G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538482 | |||||||
chr19:15538635 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0072 others(53): Show |
57 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.671+642G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538635 | |||||||
chr19:15538698 | G | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(263): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.671+705G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538698 | |||||||
chr19:15538723 | G | A | 27 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0001g0191 others(24): Show |
28 | HG00621.hp2 HG00639.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.671+730G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538723 | |||||||
chr19:15539301 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.672-1149T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539301 | |||||||
chr19:15539354 | G | A | 330 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(327): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.672-1096G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539354 | |||||||
chr19:15539451 | C | T | 354 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(351): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.672-999C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539451 | |||||||
chr19:15539465 | C | T | 2 | a0002c0003t0004g0328 a0002c0003t0004g0329 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.672-985C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539465 | |||||||
chr19:15539502 | A | G | 1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.672-948A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539502 | |||||||
chr19:15539543 | A | G | 1 | a0001c0004t0004g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.672-907A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539543 | |||||||
chr19:15539574 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(319): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.672-876C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539574 | |||||||
chr19:15540150 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.672-300G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15540150 | |||||||
chr19:15540281 | G | A | 7 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-169G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15540281 | |||||||
chr19:15540403 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0059 |
3 | HG01515.hp1 HG01517.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.672-47A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15540403 | |||||||
chr19:15540728 | GCC | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+15_939+16delCC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15540728 | ||||||
chr19:15540737 | A | AG | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+20_939+21insG | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540737 | |||||||
chr19:15540738 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+21A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540738 | |||||||
chr19:15540739 | T | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+22T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540739 | |||||||
chr19:15540742 | C | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+25C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540742 | |||||||
chr19:15540743 | T | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+26T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540743 | |||||||
chr19:15540745 | G | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+28G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540745 | |||||||
chr19:15540749 | C | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+32C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540749 | |||||||
chr19:15540751 | CG | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+35delG | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540751 | |||||||
chr19:15540753 | A | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+36A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540753 | |||||||
chr19:15540757 | C | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+40C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540757 | |||||||
chr19:15540805 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.939+88T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540805 | |||||||
chr19:15540811 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.939+94G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540811 | |||||||
chr19:15540864 | C | T | 7 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.939+147C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540864 | |||||||
chr19:15540881 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.939+164T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540881 | |||||||
chr19:15540917 | T | G | 5 | a0001c0001t0002g0051 a0001c0001t0002g0169 a0001c0001t0002g0193 others(2): Show |
5 | HG02145.hp2 HG02559.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+200T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540917 | |||||||
chr19:15540920 | A | G | 4 | a0002c0003t0004g0328 a0002c0003t0004g0329 a0002c0003t0005g0314 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+203A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540920 | |||||||
chr19:15540960 | G | A | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+243G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540960 | |||||||
chr19:15540979 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.939+262G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540979 | |||||||
chr19:15540991 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.939+274G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540991 | |||||||
chr19:15541079 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.939+362C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541079 | |||||||
chr19:15541135 | C | G | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+418C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541135 | |||||||
chr19:15541267 | A | G | 34 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0038 others(31): Show |
34 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.939+550A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541267 | |||||||
chr19:15541395 | T | C | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+678T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541395 | |||||||
chr19:15541537 | G | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0072 others(62): Show |
66 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.939+820G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541537 | |||||||
chr19:15541538 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.939+821G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541538 | |||||||
chr19:15541539 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.939+822G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541539 | |||||||
chr19:15541547 | G | C | 1 | a0001c0001t0002g0248 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+830G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541547 | |||||||
chr19:15541548 | C | A | 1 | a0001c0001t0002g0248 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+831C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541548 | |||||||
chr19:15541549 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+832A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541549 | |||||||
chr19:15541737 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0064 a0001c0001t0001g0080 others(2): Show |
5 | NA18946.hp1 NA18955.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+1020G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541737 | |||||||
chr19:15541737 | G | T | 5 | a0001c0001t0002g0051 a0001c0001t0002g0169 a0001c0001t0002g0193 others(2): Show |
5 | HG02145.hp2 HG02559.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+1020G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541737 | |||||||
chr19:15541742 | T | C | 1 | a0001c0001t0002g0248 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1025T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541742 | |||||||
chr19:15541804 | TG | T | 7 | a0001c0001t0001g0371 a0001c0001t0002g0099 a0001c0001t0002g0106 others(4): Show |
7 | HG01123.hp1 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.939+1090delG | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15541804 | ||||||
chr19:15541831 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0072 others(58): Show |
62 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.939+1114G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541831 | |||||||
chr19:15541861 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0001g0191 others(25): Show |
29 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.939+1144G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541861 | |||||||
chr19:15541865 | C | CA | 89 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0033 others(86): Show |
91 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.939+1166dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15541865 | ||||||
chr19:15541865 | C | CAA | 14 | a0001c0001t0001g0309 a0001c0001t0002g0051 a0001c0001t0002g0169 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.939+1165_939+1166d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15541865 | ||||||
chr19:15541865 | CA | C | 8 | a0001c0001t0001g0056 a0001c0001t0002g0021 a0001c0001t0003g0170 others(5): Show |
8 | HG01167.hp1 HG01168.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+1166delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15541865 | ||||||
chr19:15541877 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1160A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541877 | |||||||
chr19:15541878 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0041 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.939+1161A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541878 | |||||||
chr19:15541883 | A | G | 1 | a0001c0001t0002g0248 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1166A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541883 | |||||||
chr19:15541884 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1167G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541884 | |||||||
chr19:15542107 | C | A | 1 | a0001c0001t0003g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.939+1390C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542107 | |||||||
chr19:15542148 | A | G | 3 | a0001c0005t0002g0016 a0001c0005t0004g0018 a0001c0005t0004g0019 |
3 | HG02257.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.939+1431A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542148 | |||||||
chr19:15542187 | C | T | 28 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0001g0191 others(25): Show |
29 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.939+1470C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542187 | |||||||
chr19:15542201 | C | A | 1 | a0001c0001t0002g0047 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.939+1484C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542201 | |||||||
chr19:15542218 | T | G | 1 | a0001c0001t0002g0248 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1501T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542218 | |||||||
chr19:15542337 | G | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.939+1620G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542337 | |||||||
chr19:15542375 | T | TA | 227 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0029 others(224): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.940-1586dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15542375 | ||||||
chr19:15542389 | T | C | 25 | a0001c0001t0002g0313 a0001c0001t0002g0337 a0001c0001t0004g0122 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.940-1582T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542389 | |||||||
chr19:15542390 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.940-1581A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542390 | |||||||
chr19:15542397 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.940-1574C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542397 | |||||||
chr19:15542462 | T | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.940-1509T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542462 | |||||||
chr19:15542503 | C | G | 2 | a0002c0003t0004g0328 a0002c0003t0004g0329 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.940-1468C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542503 | |||||||
chr19:15542523 | A | G | 27 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0001g0191 others(24): Show |
28 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.940-1448A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542523 | |||||||
chr19:15542542 | A | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(292): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.940-1429A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542542 | |||||||
chr19:15542599 | G | A | 1 | a0001c0002t0002g0259 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.940-1372G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542599 | |||||||
chr19:15542715 | CT | C | 5 | a0001c0001t0002g0015 a0001c0001t0004g0011 a0001c0001t0004g0013 others(2): Show |
5 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.940-1255delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542715 | |||||||
chr19:15542746 | C | CT | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.940-1225_940-1224i others(3): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542746 | |||||||
chr19:15542756 | C | G | 1 | a0001c0001t0002g0025 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.940-1215C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542756 | |||||||
chr19:15542862 | G | C | 1 | a0001c0001t0002g0276 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.940-1109G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542862 | |||||||
chr19:15542979 | T | C | 3 | a0001c0001t0001g0239 a0001c0001t0002g0052 a0001c0001t0002g0117 |
3 | HG02056.hp1 NA18940.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.940-992T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542979 | |||||||
chr19:15543022 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0003g0212 |
2 | HG03453.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.940-949C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543022 | |||||||
chr19:15543023 | G | A | 7 | a0001c0001t0001g0376 a0001c0001t0002g0379 a0001c0001t0004g0123 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.940-948G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543023 | |||||||
chr19:15543069 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0335 |
2 | HG00741.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.940-902C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543069 | |||||||
chr19:15543070 | G | A | 1 | a0001c0001t0002g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.940-901G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543070 | |||||||
chr19:15543091 | A | G | 1 | a0001c0001t0004g0220 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.940-880A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543091 | |||||||
chr19:15543161 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.940-810G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543161 | |||||||
chr19:15543207 | C | G | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.940-764C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543207 | |||||||
chr19:15543238 | C | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0151 a0001c0001t0001g0191 others(13): Show |
17 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.940-733C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543238 | |||||||
chr19:15543248 | G | A | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.940-723G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543248 | |||||||
chr19:15543306 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0236 |
2 | HG00323.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.940-665C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543306 | |||||||
chr19:15543394 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.940-577G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543394 | |||||||
chr19:15543415 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.940-556C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543415 | |||||||
chr19:15543466 | A | G | 2 | a0001c0001t0004g0143 a0001c0001t0004g0144 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.940-505A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543466 | |||||||
chr19:15543805 | C | T | 1 | a0001c0001t0004g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.940-166C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543805 | |||||||
chr19:15543820 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0029 others(219): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.940-151G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543820 | |||||||
chr19:15543821 | C | T | 1 | a0001c0005t0002g0016 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.940-150C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543821 | |||||||
chr19:15543858 | GA | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0033 a0001c0001t0001g0063 others(85): Show |
90 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.940-94delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15543858 | ||||||
chr19:15543858 | GAA | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(191): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.940-95_940-94delAA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15543858 | ||||||
chr19:15544325 | G | A | 1 | a0003c0007t0004g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1136+46G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544325 | |||||||
chr19:15544342 | C | G | 25 | a0001c0001t0002g0313 a0001c0001t0002g0337 a0001c0001t0004g0122 others(22): Show |
26 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1136+63C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544342 | |||||||
chr19:15544357 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(292): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1136+78C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544357 | |||||||
chr19:15544394 | T | G | 1 | a0001c0001t0001g0351 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1136+115T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544394 | |||||||
chr19:15544474 | G | A | 4 | a0001c0001t0001g0340 a0001c0001t0001g0357 a0001c0001t0001g0360 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+195G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544474 | |||||||
chr19:15544499 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0041 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.1136+220A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544499 | |||||||
chr19:15544521 | C | A | 1 | a0001c0001t0002g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1136+242C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544521 | |||||||
chr19:15544738 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1136+459C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544738 | |||||||
chr19:15544798 | C | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(293): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1136+519C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544798 | |||||||
chr19:15544846 | A | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1136+567A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544846 | |||||||
chr19:15544899 | A | G | 5 | a0001c0001t0002g0015 a0001c0001t0004g0011 a0001c0001t0004g0013 others(2): Show |
5 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136+620A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544899 | |||||||
chr19:15544933 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.1136+654T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544933 | |||||||
chr19:15544948 | C | T | 35 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0038 others(32): Show |
35 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1136+669C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544948 | |||||||
chr19:15544953 | C | T | 1 | a0001c0002t0003g0264 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1136+674C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544953 | |||||||
chr19:15545027 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0026 others(288): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1136+748C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545027 | |||||||
chr19:15545104 | T | TA | 222 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1136+837dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545104 | ||||||
chr19:15545104 | T | TAA | 10 | a0001c0001t0002g0021 a0001c0001t0002g0051 a0001c0001t0002g0169 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+836_1136+837d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545104 | ||||||
chr19:15545108 | A | AT | 31 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0038 others(28): Show |
31 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1136+829_1136+830i others(3): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545108 | |||||||
chr19:15545114 | A | AC | 8 | a0001c0001t0002g0337 a0001c0001t0004g0122 a0001c0001t0004g0141 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1136+835_1136+836i others(3): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545114 | |||||||
chr19:15545234 | CAT | C | 5 | a0001c0001t0002g0004 a0001c0001t0002g0248 a0001c0001t0002g0249 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1136+958_1136+959d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545234 | ||||||
chr19:15545327 | A | G | 1 | a0010c0018t0002g0378 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1136+1048A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545327 | |||||||
chr19:15545328 | G | C | 27 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0038 others(24): Show |
27 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1136+1049G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545328 | |||||||
chr19:15545395 | T | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(343): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1136+1116T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545395 | |||||||
chr19:15545570 | AC | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0062 others(75): Show |
79 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1136+1294delC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545570 | ||||||
chr19:15545582 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1136+1303G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545582 | |||||||
chr19:15545590 | G | T | 12 | a0001c0001t0002g0021 a0001c0001t0002g0060 a0001c0001t0002g0099 others(9): Show |
13 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1136+1311G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545590 | |||||||
chr19:15545648 | C | CA | 47 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0001g0151 others(44): Show |
47 | HG00408.hp1 HG00558.hp2 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.1136+1392dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAA | 6 | a0001c0001t0002g0319 a0001c0001t0003g0002 a0001c0001t0003g0154 others(3): Show |
7 | HG00639.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136+1390_1136+139 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAAA | 21 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0042 others(18): Show |
21 | HG00621.hp2 HG00642.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1136+1389_1136+139 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAAAAA | 11 | a0001c0001t0001g0003 a0001c0001t0002g0085 a0001c0001t0002g0087 others(8): Show |
12 | HG01070.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136+1387_1136+139 others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAAAAAA | 32 | a0001c0001t0001g0033 a0001c0001t0002g0020 a0001c0001t0002g0022 others(29): Show |
32 | HG00558.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1136+1386_1136+139 others(11): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAAAAAA others(1): Show |
16 | a0001c0001t0001g0222 a0001c0001t0002g0031 a0001c0001t0002g0065 others(13): Show |
16 | HG00673.hp1 HG01123.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1136+1385_1136+139 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0369 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1136+1381_1136+139 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0371 a0002c0003t0003g0005 a0005c0006t0005g0009 |
4 | HG01123.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+1380_1136+139 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAAAAAA others(7): Show |
5 | a0001c0001t0002g0060 a0002c0003t0002g0007 a0002c0003t0002g0008 others(2): Show |
5 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+1379_1136+139 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545648 | C | CAAAAAAA others(8): Show |
2 | a0005c0006t0005g0302 a0006c0016t0005g0109 |
2 | HG01109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1136+1378_1136+139 others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | ||||||
chr19:15545659 | AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0245 a0001c0002t0002g0259 others(1): Show |
4 | HG02257.hp1 HG03239.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136+1385_1136+139 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545659 | ||||||
chr19:15545661 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0002g0337 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1136+1387_1136+139 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545661 | ||||||
chr19:15545667 | A | AAAAAAGA others(4): Show |
1 | a0001c0001t0002g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1136+1392_1136+139 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545667 | ||||||
chr19:15545667 | A | G | 6 | a0001c0001t0003g0212 a0001c0001t0004g0192 a0001c0002t0003g0010 others(3): Show |
6 | HG02717.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1136+1388A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545667 | |||||||
chr19:15545672 | G | A | 64 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0038 others(61): Show |
66 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.1136+1393G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545672 | |||||||
chr19:15545677 | G | A | 17 | a0001c0001t0001g0037 a0001c0001t0001g0056 a0001c0001t0001g0059 others(14): Show |
17 | HG00408.hp2 HG00733.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136+1398G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545677 | |||||||
chr19:15545678 | A | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0041 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1136+1399A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545678 | |||||||
chr19:15545679 | AAAGAAAA others(6): Show |
A | 5 | a0001c0001t0003g0212 a0001c0001t0004g0192 a0001c0002t0003g0010 others(2): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136+1408_1136+142 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545679 | ||||||
chr19:15545683 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1136+1404A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545683 | |||||||
chr19:15545683 | A | T | 45 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0042 others(42): Show |
47 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1136+1404A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545683 | |||||||
chr19:15545688 | A | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0056 a0001c0001t0001g0059 others(6): Show |
9 | HG00733.hp1 HG01517.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1136+1409A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545688 | |||||||
chr19:15545689 | AAAG | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0041 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1136+1416_1136+141 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545689 | ||||||
chr19:15545692 | G | GAA | 116 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0033 others(113): Show |
119 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.1136+1414_1136+141 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545692 | ||||||
chr19:15545692 | G | GAAAAGAA | 13 | a0001c0001t0001g0037 a0001c0001t0001g0056 a0001c0001t0001g0059 others(10): Show |
13 | HG00733.hp1 HG01517.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1136+1415_1136+141 others(11): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545692 | ||||||
chr19:15545692 | G | GAAAAGAA others(5): Show |
3 | a0001c0001t0002g0054 a0001c0001t0002g0058 a0001c0001t0002g0311 |
3 | HG03041.hp2 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1136+1415_1136+141 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545692 | ||||||
chr19:15545708 | G | A | 4 | a0001c0001t0001g0226 a0001c0001t0001g0240 a0001c0001t0001g0253 others(1): Show |
4 | HG00544.hp1 HG02132.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+1429G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545708 | |||||||
chr19:15545795 | G | A | 21 | a0001c0001t0002g0015 a0001c0001t0003g0301 a0001c0001t0003g0303 others(18): Show |
21 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1136+1516G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545795 | |||||||
chr19:15545802 | G | A | 13 | a0001c0001t0002g0021 a0001c0001t0002g0099 a0001c0001t0002g0337 others(10): Show |
13 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1136+1523G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545802 | |||||||
chr19:15545861 | G | A | 5 | a0001c0004t0001g0089 a0001c0004t0001g0091 a0001c0004t0001g0093 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+1582G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545861 | |||||||
chr19:15545873 | G | C | 3 | a0001c0002t0003g0010 a0001c0004t0002g0178 a0005c0006t0002g0320 |
3 | HG02717.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1136+1594G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545873 | |||||||
chr19:15545948 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1136+1669T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545948 | |||||||
chr19:15546039 | A | C | 1 | a0001c0002t0003g0010 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1136+1760A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546039 | |||||||
chr19:15546302 | G | A | 65 | a0001c0001t0001g0309 a0001c0001t0002g0020 a0001c0001t0002g0022 others(62): Show |
65 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1137-1806G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546302 | |||||||
chr19:15546601 | C | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1137-1507C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546601 | |||||||
chr19:15546614 | ACTAAT | A | 5 | a0005c0006t0002g0320 a0005c0006t0005g0009 a0005c0006t0005g0302 others(2): Show |
5 | HG01109.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-1485_1137-148 others(9): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15546614 | ||||||
chr19:15546891 | G | T | 1 | a0001c0001t0002g0066 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1137-1217G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546891 | |||||||
chr19:15546956 | T | C | 2 | a0001c0001t0004g0220 a0001c0001t0009g0012 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1137-1152T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546956 | |||||||
chr19:15546963 | G | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1137-1145G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546963 | |||||||
chr19:15546992 | T | C | 21 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0038 others(18): Show |
21 | HG00642.hp1 HG00733.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1137-1116T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546992 | |||||||
chr19:15547018 | G | GT | 11 | a0001c0001t0003g0164 a0001c0001t0003g0167 a0001c0001t0003g0181 others(8): Show |
12 | HG00733.hp2 HG01175.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1137-1068dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTT | 32 | a0001c0001t0003g0027 a0001c0001t0003g0303 a0001c0001t0004g0011 others(29): Show |
32 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1137-1069_1137-106 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTT | 13 | a0001c0001t0002g0051 a0001c0001t0002g0053 a0001c0001t0002g0130 others(10): Show |
13 | HG01070.hp1 HG02145.hp2 HG03579.hp1 others(10): Show |
intron_variant | MODIFIER | c.1137-1072_1137-106 others(9): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(1): Show |
72 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(69): Show |
72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1137-1075_1137-106 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(2): Show |
58 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0043 others(55): Show |
59 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1137-1076_1137-106 others(13): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(3): Show |
13 | a0001c0001t0001g0042 a0001c0001t0001g0171 a0001c0001t0001g0195 others(10): Show |
13 | HG00140.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1137-1077_1137-106 others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0343 a0001c0001t0001g0360 a0002c0003t0001g0317 |
3 | HG00099.hp1 HG02280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1137-1078_1137-106 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0151 a0001c0001t0012g0118 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1137-1079_1137-106 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(6): Show |
14 | a0001c0001t0002g0032 a0001c0001t0002g0035 a0001c0001t0002g0039 others(11): Show |
14 | HG00609.hp2 HG00735.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1137-1080_1137-106 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(7): Show |
30 | a0001c0001t0002g0015 a0001c0001t0002g0020 a0001c0001t0002g0022 others(27): Show |
30 | HG00408.hp1 HG00558.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1137-1081_1137-106 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(8): Show |
19 | a0001c0001t0002g0030 a0001c0001t0002g0034 a0001c0001t0002g0065 others(16): Show |
19 | HG00673.hp1 HG01081.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.1137-1082_1137-106 others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(9): Show |
8 | a0001c0001t0002g0108 a0001c0001t0002g0121 a0001c0001t0002g0172 others(5): Show |
8 | HG01358.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-1083_1137-106 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0005g0225 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1137-1084_1137-106 others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(11): Show |
3 | a0001c0001t0002g0100 a0001c0001t0002g0379 a0006c0017t0002g0364 |
3 | HG02809.hp2 HG03453.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1137-1085_1137-106 others(22): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(12): Show |
3 | a0001c0001t0002g0087 a0002c0003t0005g0327 a0006c0016t0005g0109 |
3 | HG01109.hp1 HG03130.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1137-1086_1137-106 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(13): Show |
2 | a0002c0003t0005g0314 a0005c0006t0005g0302 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1137-1087_1137-106 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(14): Show |
1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1137-1088_1137-106 others(25): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(16): Show |
2 | a0001c0005t0004g0019 a0003c0007t0004g0097 |
2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1137-1068_1137-106 others(27): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(17): Show |
1 | a0001c0005t0004g0018 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1137-1068_1137-106 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(18): Show |
1 | a0001c0001t0004g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1137-1068_1137-106 others(29): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | G | GTTTTTTT others(23): Show |
1 | a0011c0015t0004g0205 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1137-1068_1137-106 others(34): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547018 | GT | G | 20 | a0001c0001t0002g0004 a0001c0001t0002g0023 a0001c0001t0002g0049 others(17): Show |
21 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1137-1068delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | ||||||
chr19:15547074 | A | C | 1 | a0001c0001t0012g0118 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1137-1034A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547074 | |||||||
chr19:15547078 | T | C | 1 | a0001c0001t0009g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1137-1030T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547078 | |||||||
chr19:15547109 | C | T | 23 | a0001c0001t0002g0004 a0001c0001t0002g0023 a0001c0001t0002g0047 others(20): Show |
24 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1137-999C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547109 | |||||||
chr19:15547117 | G | A | 3 | a0001c0001t0002g0053 a0001c0001t0002g0099 a0008c0010t0002g0238 |
3 | HG01361.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1137-991G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547117 | |||||||
chr19:15547123 | A | C | 15 | a0001c0001t0002g0051 a0001c0001t0002g0130 a0001c0001t0002g0163 others(12): Show |
15 | HG01070.hp1 HG02145.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137-985A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547123 | |||||||
chr19:15547228 | T | C | 23 | a0001c0001t0002g0004 a0001c0001t0002g0023 a0001c0001t0002g0047 others(20): Show |
24 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1137-880T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547228 | |||||||
chr19:15547266 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1137-842C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547266 | |||||||
chr19:15547282 | T | C | 11 | a0001c0001t0004g0220 a0001c0001t0005g0185 a0001c0001t0009g0012 others(8): Show |
11 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1137-826T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547282 | |||||||
chr19:15547411 | C | A | 1 | a0002c0003t0002g0361 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-697C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547411 | |||||||
chr19:15547560 | C | A | 2 | a0001c0001t0004g0220 a0001c0001t0009g0012 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1137-548C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547560 | |||||||
chr19:15547588 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1137-520C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547588 | |||||||
chr19:15547639 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1137-469A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547639 | |||||||
chr19:15547648 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137-460C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547648 | |||||||
chr19:15547771 | C | T | 1 | a0001c0004t0004g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1137-337C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547771 | |||||||
chr19:15547777 | G | T | 1 | a0001c0001t0012g0118 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1137-331G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547777 | |||||||
chr19:15547803 | C | G | 1 | a0001c0001t0009g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1137-305C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547803 | |||||||
chr19:15547817 | G | A | 1 | a0003c0007t0001g0281 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1137-291G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547817 | |||||||
chr19:15547921 | T | C | 1 | a0001c0001t0002g0319 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1137-187T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547921 | |||||||
chr19:15547968 | T | TGA | 3 | a0001c0001t0002g0022 a0001c0001t0002g0197 a0001c0001t0005g0185 |
3 | HG00609.hp2 HG04184.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1137-114_1137-113d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547968 | ||||||
chr19:15547968 | TGA | T | 9 | a0001c0001t0001g0367 a0001c0001t0003g0170 a0001c0001t0003g0179 others(6): Show |
10 | HG00738.hp1 HG01168.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-114_1137-113d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547968 | ||||||
chr19:15547982 | AGAGAGAG others(7): Show |
A | 1 | a0001c0001t0008g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1137-118_1137-105d others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547982 | ||||||
chr19:15547984 | AGAGAGAG others(5): Show |
A | 1 | a0001c0001t0001g0135 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1137-116_1137-105d others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547984 | ||||||
chr19:15547986 | AGAGAGAG others(3): Show |
A | 36 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0073 others(33): Show |
36 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1137-114_1137-105d others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547986 | ||||||
chr19:15547988 | AGAGAGAG others(1): Show |
A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0064 a0001c0001t0001g0210 others(15): Show |
18 | HG00544.hp1 HG00621.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-112_1137-105d others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547988 | ||||||
chr19:15547988 | AGAGAGAG others(9): Show |
A | 5 | a0001c0001t0004g0192 a0001c0001t0007g0316 a0001c0004t0007g0045 others(2): Show |
5 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-118_1137-103d others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547988 | ||||||
chr19:15547988 | AGAGAGAG others(11): Show |
A | 4 | a0001c0005t0004g0018 a0001c0005t0004g0019 a0003c0007t0004g0097 others(1): Show |
4 | HG02572.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-118_1137-101d others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547988 | ||||||
chr19:15547988 | AGAGAGAG others(17): Show |
A | 2 | a0001c0001t0002g0157 a0001c0002t0002g0105 |
2 | HG01243.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1137-118_1137-95de others(25): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547988 | ||||||
chr19:15547990 | AGAGAGG | A | 33 | a0001c0001t0001g0006 a0001c0001t0001g0074 a0001c0001t0001g0191 others(30): Show |
33 | HG00558.hp2 HG00735.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1137-112_1137-107d others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547990 | ||||||
chr19:15547990 | AGAGAGGG others(7): Show |
A | 1 | a0001c0001t0001g0067 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1137-116_1137-103d others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547990 | ||||||
chr19:15547992 | A | AGG | 2 | a0001c0001t0003g0002 a0001c0001t0003g0027 |
3 | HG00621.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1137-115_1137-114i others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGG | A | 20 | a0001c0001t0001g0080 a0001c0001t0001g0376 a0001c0001t0002g0020 others(17): Show |
20 | HG00558.hp1 HG01081.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1137-112_1137-109d others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGGGAG others(5): Show |
A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(45): Show |
48 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.1137-114_1137-103d others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGGGAG others(7): Show |
A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0063 a0001c0001t0001g0151 others(6): Show |
9 | HG00741.hp2 HG01123.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-114_1137-101d others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGGGAG others(9): Show |
A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0056 a0001c0001t0001g0057 others(6): Show |
10 | HG00642.hp1 HG01109.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1137-114_1137-99de others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGGGAG others(11): Show |
A | 2 | a0001c0001t0002g0248 a0001c0001t0002g0344 |
2 | HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1137-114_1137-97de others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGGGAG others(13): Show |
A | 13 | a0001c0001t0002g0004 a0001c0001t0002g0047 a0001c0001t0002g0147 others(10): Show |
14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1137-114_1137-95de others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGGGAG others(15): Show |
A | 2 | a0001c0001t0002g0102 a0001c0001t0002g0255 |
2 | HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1137-114_1137-93de others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGGGAG others(17): Show |
A | 1 | a0001c0001t0001g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1137-114_1137-91de others(25): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547992 | AGAGGGAG others(21): Show |
A | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1137-114_1137-87de others(29): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | ||||||
chr19:15547994 | A | G | 3 | a0001c0001t0003g0154 a0001c0001t0003g0158 a0001c0001t0003g0355 |
3 | HG00140.hp2 HG00639.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1137-114A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547994 | |||||||
chr19:15547994 | AGG | A | 5 | a0001c0001t0002g0095 a0001c0001t0002g0117 a0001c0001t0002g0269 others(2): Show |
5 | HG01358.hp2 HG01515.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-112_1137-111d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | ||||||
chr19:15547994 | AGGGAGAG others(3): Show |
A | 10 | a0001c0001t0001g0033 a0001c0001t0001g0171 a0001c0001t0001g0189 others(7): Show |
10 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-112_1137-103d others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | ||||||
chr19:15547994 | AGGGAGAG others(5): Show |
A | 16 | a0001c0001t0001g0029 a0001c0001t0001g0103 a0001c0001t0001g0114 others(13): Show |
16 | HG00735.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1137-112_1137-101d others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | ||||||
chr19:15547994 | AGGGAGAG others(7): Show |
A | 24 | a0001c0001t0002g0015 a0001c0001t0004g0011 a0001c0001t0004g0013 others(21): Show |
24 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1137-112_1137-99de others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | ||||||
chr19:15547994 | AGGGAGAG others(9): Show |
A | 15 | a0001c0001t0002g0025 a0001c0001t0002g0106 a0001c0001t0002g0125 others(12): Show |
15 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1137-112_1137-97de others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | ||||||
chr19:15547994 | AGGGAGAG others(11): Show |
A | 1 | a0001c0001t0002g0023 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1137-112_1137-95de others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | ||||||
chr19:15547994 | AGGGAGAG others(13): Show |
A | 4 | a0001c0001t0002g0049 a0001c0001t0002g0129 a0001c0001t0002g0290 others(1): Show |
4 | HG01952.hp1 HG02735.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-112_1137-93de others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | ||||||
chr19:15547996 | G | A | 44 | a0001c0001t0002g0021 a0001c0001t0002g0048 a0001c0001t0002g0051 others(41): Show |
45 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1137-112G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547996 | |||||||
chr19:15547996 | G | T | 3 | a0001c0001t0001g0367 a0001c0001t0002g0022 a0001c0001t0002g0197 |
3 | HG00609.hp2 HG04184.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1137-112G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547996 | |||||||
chr19:15547998 | A | T | 8 | a0001c0001t0001g0080 a0001c0001t0001g0367 a0001c0001t0001g0376 others(5): Show |
8 | HG00609.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-110A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547998 | |||||||
chr19:15547998 | AGAGAGTG others(7): Show |
A | 1 | a0001c0001t0004g0220 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1137-108_1137-95de others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547998 | ||||||
chr19:15548000 | A | T | 16 | a0001c0001t0001g0080 a0001c0001t0001g0241 a0001c0001t0001g0246 others(13): Show |
17 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.1137-108A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548000 | |||||||
chr19:15548002 | A | AGAGTGTG others(3): Show |
1 | a0001c0002t0002g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1137-105_1137-104i others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548002 | A | AGT | 17 | a0001c0001t0003g0040 a0001c0001t0003g0046 a0001c0001t0003g0050 others(14): Show |
17 | HG01081.hp2 HG01109.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1137-59_1137-58dup others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548002 | A | AGTGT | 8 | a0001c0001t0003g0055 a0001c0001t0003g0212 a0001c0001t0003g0295 others(5): Show |
8 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-61_1137-58dup others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548002 | A | AGTGTGTG others(3): Show |
3 | a0001c0001t0002g0053 a0001c0001t0003g0352 a0002c0003t0003g0362 |
3 | HG01167.hp1 HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1137-67_1137-58dup others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548002 | A | T | 41 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0064 others(38): Show |
42 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1137-106A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548002 | |||||||
chr19:15548002 | AGT | A | 8 | a0001c0001t0003g0152 a0001c0001t0003g0181 a0001c0001t0003g0230 others(5): Show |
9 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-59_1137-58del others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548002 | AGTGT | A | 3 | a0001c0001t0002g0224 a0001c0001t0002g0353 a0002c0003t0002g0361 |
3 | HG02818.hp2 HG03927.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1137-61_1137-58del others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548002 | AGTGTGT | A | 8 | a0001c0001t0002g0130 a0001c0001t0002g0211 a0001c0001t0002g0217 others(5): Show |
8 | HG01070.hp1 HG03225.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-63_1137-58del others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548002 | AGTGTGTG others(1): Show |
A | 5 | a0001c0001t0002g0051 a0001c0001t0002g0169 a0001c0001t0002g0193 others(2): Show |
5 | HG02145.hp2 HG02559.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-65_1137-58del others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548002 | AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0003g0164 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1137-67_1137-58del others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | ||||||
chr19:15548004 | T | A | 20 | a0001c0001t0002g0030 a0001c0001t0002g0052 a0001c0001t0002g0060 others(17): Show |
20 | HG01358.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1137-104T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548004 | |||||||
chr19:15548006 | T | A | 10 | a0001c0001t0002g0095 a0001c0001t0002g0096 a0001c0001t0002g0108 others(7): Show |
10 | HG00408.hp1 HG01358.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-102T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548006 | |||||||
chr19:15548008 | T | A | 8 | a0001c0001t0001g0114 a0001c0001t0002g0095 a0001c0001t0002g0224 others(5): Show |
8 | HG01358.hp2 HG01515.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-100T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548008 | |||||||
chr19:15548010 | T | A | 11 | a0001c0001t0002g0015 a0001c0001t0002g0130 a0001c0001t0002g0211 others(8): Show |
11 | HG01070.hp1 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1137-98T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548010 | |||||||
chr19:15548012 | T | A | 15 | a0001c0001t0002g0106 a0001c0001t0002g0125 a0001c0001t0002g0130 others(12): Show |
15 | HG01070.hp1 HG01891.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137-96T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548012 | |||||||
chr19:15548016 | T | A | 1 | a0001c0001t0002g0379 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1137-92T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548016 | |||||||
chr19:15548041 | G | T | 2 | a0001c0001t0004g0220 a0001c0001t0009g0012 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1137-67G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548041 | |||||||
chr19:15548049 | GT | G | 7 | a0001c0001t0001g0063 a0001c0001t0001g0159 a0001c0001t0001g0253 others(4): Show |
7 | HG00544.hp1 HG01123.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1137-55delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548049 | ||||||
chr19:15548081 | C | G | 1 | a0010c0018t0002g0378 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1137-27C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548081 | |||||||
chr19:15548257 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1270+16C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548257 | |||||||
chr19:15548372 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0196 a0001c0001t0001g0222 others(5): Show |
9 | HG02015.hp2 HG02071.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1270+131T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548372 | |||||||
chr19:15548382 | G | A | 3 | a0001c0001t0002g0053 a0001c0001t0002g0099 a0008c0010t0002g0238 |
3 | HG01361.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1270+141G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548382 | |||||||
chr19:15548384 | G | T | 2 | a0001c0001t0004g0220 a0001c0001t0009g0012 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1270+143G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548384 | |||||||
chr19:15548405 | G | C | 5 | a0001c0001t0002g0036 a0001c0001t0002g0065 a0001c0001t0002g0066 others(2): Show |
5 | HG00408.hp2 HG00673.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+164G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548405 | |||||||
chr19:15548427 | G | T | 11 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0064 others(8): Show |
11 | HG02683.hp1 HG03704.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.1270+186G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548427 | |||||||
chr19:15548643 | A | G | 1 | a0001c0001t0001g0346 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1270+402A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548643 | |||||||
chr19:15548660 | A | G | 3 | a0001c0001t0005g0185 a0002c0003t0005g0314 a0002c0003t0005g0327 |
3 | HG02965.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1270+419A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548660 | |||||||
chr19:15548766 | G | A | 2 | a0001c0001t0004g0220 a0001c0001t0009g0012 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1271-372G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548766 | |||||||
chr19:15548949 | G | A | 2 | a0001c0001t0004g0220 a0001c0001t0009g0012 |
2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1271-189G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548949 | |||||||
chr19:15549219 | C | G | 5 | a0001c0001t0004g0220 a0001c0001t0005g0185 a0001c0001t0009g0012 others(2): Show |
5 | HG02559.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335+17C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549219 | |||||||
chr19:15549286 | G | T | 1 | a0001c0001t0012g0118 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1335+84G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549286 | |||||||
chr19:15549488 | AT | A | 9 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0106 others(6): Show |
9 | HG01891.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335+287delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549488 | |||||||
chr19:15549563 | C | A | 1 | a0001c0001t0001g0371 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1335+361C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549563 | |||||||
chr19:15549592 | C | T | 1 | a0001c0001t0004g0220 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1335+390C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549592 | |||||||
chr19:15549773 | C | T | 1 | a0001c0001t0009g0012 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1335+571C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549773 | |||||||
chr19:15549804 | T | TA | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(187): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1335+615dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 15549804 | ||||||
chr19:15549815 | A | C | 1 | a0002c0003t0002g0361 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1335+613A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549815 | |||||||
chr19:15549824 | C | A | 1 | a0002c0003t0002g0361 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1335+622C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549824 | |||||||
chr19:15549992 | G | A | 1 | a0001c0001t0004g0220 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1336-682G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549992 | |||||||
chr19:15550034 | T | A | 1 | a0002c0003t0001g0374 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1336-640T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550034 | |||||||
chr19:15550134 | T | C | 3 | a0001c0001t0005g0185 a0002c0003t0005g0314 a0002c0003t0005g0327 |
3 | HG02965.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1336-540T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550134 | |||||||
chr19:15550247 | C | A | 2 | a0001c0001t0002g0021 a0001c0002t0002g0310 |
2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1336-427C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550247 | |||||||
chr19:15550285 | TAACA | T | 5 | a0001c0001t0001g0376 a0001c0004t0001g0089 a0001c0004t0001g0091 others(2): Show |
5 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-370_1336-367d others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 15550285 | ||||||
chr19:15550285 | TAACAAAC others(1): Show |
T | 3 | a0001c0001t0004g0220 a0001c0001t0009g0012 a0001c0001t0012g0118 |
3 | HG02258.hp2 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1336-374_1336-367d others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 15550285 | ||||||
chr19:15550322 | C | A | 3 | a0001c0001t0005g0185 a0002c0003t0005g0314 a0002c0003t0005g0327 |
3 | HG02965.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1336-352C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550322 | |||||||
chr19:15550327 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1336-347A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550327 | |||||||
chr19:15550341 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1336-333G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550341 | |||||||
chr19:15550368 | T | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(185): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1336-306T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550368 | |||||||
chr19:15550485 | C | T | 1 | a0001c0001t0004g0220 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1336-189C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550485 | |||||||
chr19:15550497 | T | A | 4 | a0001c0005t0004g0018 a0001c0005t0004g0019 a0003c0007t0004g0097 others(1): Show |
4 | HG02572.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-177T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550497 | |||||||
chr19:15550572 | CT | C | 51 | a0001c0001t0002g0020 a0001c0001t0002g0022 a0001c0001t0002g0030 others(48): Show |
51 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1336-101delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550572 | |||||||
chr19:15550893 | A | G | 1 | a0010c0018t0002g0378 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1418+137A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 13/13 | chr19 | 15550893 | |||||||
chr19:15551065 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.1419-229A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 13/13 | chr19 | 15551065 | |||||||
chr19:15551107 | T | C | 1 | a0001c0001t0002g0176 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1419-187T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 13/13 | chr19 | 15551107 | |||||||
chr19:15551235 | C | G | 2 | a0001c0001t0009g0012 a0001c0001t0012g0118 |
2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1419-59C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 13/13 | chr19 | 15551235 |