geneid | 4051 |
---|---|
ensemblid | ENSG00000186529.16 |
hgncid | 2646 |
symbol | CYP4F3 |
name | cytochrome P450 family 4 subfamily F member 3 |
refseq_nuc | NM_000896.3 |
refseq_prot | NP_000887.2 |
ensembl_nuc | ENST00000221307.13 |
ensembl_prot | ENSP00000221307.6 |
mane_status | MANE Select |
chr | chr19 |
start | 15640897 |
end | 15662825 |
strand | + |
ver | v1.2 |
region | chr19:15640897-15662825 |
region5000 | chr19:15635897-15667825 |
regionname0 | CYP4F3_chr19_15640897_15662825 |
regionname5000 | CYP4F3_chr19_15635897_15667825 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 520 | 336 | 82 | 64 | 135 | 12 | 41 | 105 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002 | 0/0 | 520 | 64 | 8 | 8 | 39 | 3 | 6 | 32 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0003 | 0/0 | 520 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0004 | 0/0 | 520 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0005 | 0/0 | 520 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0006 | 0/0 | 520 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0007 | 0/0 | 520 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0008 | 0/0 | 520 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0009 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0010 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0011 | 0/0 | 520 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0012 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0013 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0014 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0015 | 0/0 | 520 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0016 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1563 | 174 | 52 | 27 | 84 | 1 | 10 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0002 | 1/1 | 1563 | 86 | 17 | 21 | 19 | 9 | 18 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0003 | 0/0 | 1563 | 60 | 8 | 8 | 35 | 3 | 6 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0004 | 0/0 | 1563 | 41 | 8 | 6 | 19 | 0 | 8 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0005 | 0/0 | 1563 | 31 | 3 | 9 | 12 | 2 | 5 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0006 | 0/0 | 1563 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0007 | 0/0 | 1563 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0008 | 0/0 | 1563 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0009 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0010 | 0/0 | 1563 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0011 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0012 | 0/0 | 1563 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0013 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0014 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0015 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0016 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0017 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0018 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0019 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0020 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0021 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0022 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
c0023 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3490 | 84 | 8 | 20 | 28 | 10 | 16 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0002 | 0/0 | 3496 | 74 | 0 | 15 | 51 | 1 | 7 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0003 | 0/0 | 3486 | 55 | 6 | 8 | 35 | 1 | 5 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0004 | 0/0 | 3489 | 28 | 2 | 10 | 10 | 2 | 4 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0005 | 0/0 | 3498 | 16 | 2 | 3 | 8 | 0 | 3 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0006 | 0/0 | 3497 | 15 | 0 | 4 | 11 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0007 | 0/0 | 3499 | 11 | 2 | 1 | 7 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0008 | 0/0 | 3506 | 9 | 5 | 4 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0009 | 0/0 | 3504 | 8 | 8 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0010 | 0/0 | 3507 | 7 | 3 | 2 | 0 | 1 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0011 | 0/0 | 3500 | 5 | 0 | 0 | 2 | 0 | 3 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0012 | 0/0 | 3505 | 5 | 4 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0013 | 0/0 | 3509 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0014 | 0/0 | 3495 | 4 | 0 | 1 | 3 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0015 | 0/0 | 3509 | 4 | 2 | 1 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0016 | 0/0 | 3504 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0017 | 0/0 | 3513 | 4 | 2 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0018 | 0/0 | 3508 | 4 | 3 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0019 | 0/0 | 3508 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0020 | 0/0 | 3507 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0021 | 0/0 | 3495 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0022 | 0/0 | 3506 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0023 | 0/0 | 3500 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0024 | 0/0 | 3495 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0025 | 0/0 | 3490 | 2 | 0 | 0 | 1 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0026 | 0/0 | 3496 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0027 | 0/0 | 3496 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0028 | 0/0 | 3485 | 2 | 1 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0029 | 0/0 | 3488 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0030 | 0/0 | 3514 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0031 | 0/0 | 3491 | 2 | 0 | 1 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0032 | 0/0 | 3490 | 2 | 1 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0033 | 0/0 | 3506 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0034 | 0/0 | 3492 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0035 | 0/0 | 3497 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0036 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0037 | 0/0 | 3500 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0038 | 0/0 | 3493 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0039 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0040 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0041 | 0/0 | 3504 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0042 | 0/0 | 3497 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0043 | 0/0 | 3486 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0044 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0045 | 0/0 | 3490 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0046 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0047 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0048 | 0/0 | 3493 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0049 | 0/0 | 3505 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0050 | 0/0 | 3496 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0051 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0052 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0053 | 0/0 | 3512 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0054 | 0/0 | 3511 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0055 | 0/0 | 3507 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0056 | 0/0 | 3500 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0057 | 0/0 | 3498 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0058 | 0/0 | 3496 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0059 | 0/0 | 3497 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0060 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0061 | 0/0 | 3487 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0062 | 0/0 | 3497 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0063 | 0/0 | 3486 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0064 | 0/0 | 3487 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0065 | 0/0 | 3487 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0066 | 0/0 | 3485 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0067 | 0/0 | 3490 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0068 | 0/0 | 3516 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0069 | 0/0 | 3512 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0070 | 0/0 | 3495 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0071 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0072 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0073 | 0/0 | 3488 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0074 | 0/0 | 3488 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0075 | 0/0 | 3489 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0076 | 0/0 | 3490 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0077 | 0/0 | 3490 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0078 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0079 | 0/0 | 3496 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0080 | 0/0 | 3496 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0081 | 0/0 | 3499 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0082 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0083 | 0/0 | 3501 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
t0084 | 0/0 | 3506 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0378 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0403 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0405 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0406 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0407 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0408 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0409 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0411 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1563 | 174 | 52 | 27 | 84 | 1 | 10 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002 | 1/1 | 1563 | 86 | 17 | 21 | 19 | 9 | 18 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004 | 0/0 | 1563 | 41 | 8 | 6 | 19 | 0 | 8 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0005 | 0/0 | 1563 | 31 | 3 | 9 | 12 | 2 | 5 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0010 | 0/0 | 1563 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0018 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0021 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003 | 0/0 | 1563 | 60 | 8 | 8 | 35 | 3 | 6 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0007 | 0/0 | 1563 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0003c0006 | 0/0 | 1563 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0004c0008 | 0/0 | 1563 | 4 | 0 | 0 | 4 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0005c0011 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0006c0012 | 0/0 | 1563 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0007c0009 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0008c0013 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0009c0014 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0010c0023 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0011c0016 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0012c0017 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0013c0015 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0014c0020 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0015c0019 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0016c0022 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 5058 | 71 | 0 | 15 | 49 | 1 | 6 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0003 | 0/0 | 5048 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0006 | 0/0 | 5059 | 13 | 0 | 3 | 10 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0008 | 0/0 | 5068 | 7 | 3 | 4 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0009 | 0/0 | 5066 | 8 | 8 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0010 | 0/0 | 5069 | 6 | 3 | 2 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0012 | 0/0 | 5067 | 5 | 4 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0013 | 0/0 | 5071 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0014 | 0/0 | 5057 | 4 | 0 | 1 | 3 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0015 | 0/0 | 5071 | 4 | 2 | 1 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0016 | 0/0 | 5066 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0018 | 0/0 | 5070 | 4 | 3 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0019 | 0/0 | 5070 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0020 | 0/0 | 5069 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0022 | 0/0 | 5068 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0024 | 0/0 | 5057 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0025 | 0/0 | 5052 | 2 | 0 | 0 | 1 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0026 | 0/0 | 5058 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0027 | 0/0 | 5058 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0033 | 0/0 | 5068 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0035 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0036 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0040 | 0/0 | 5063 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0044 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0046 | 0/0 | 5068 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0047 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0048 | 0/0 | 5055 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0049 | 0/0 | 5067 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0050 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0054 | 0/0 | 5073 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0055 | 0/0 | 5069 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0056 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0057 | 0/0 | 5060 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0058 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0059 | 0/0 | 5059 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0060 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0062 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0077 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0078 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0079 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0080 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0082 | 0/0 | 5064 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0083 | 0/0 | 5063 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0001t0084 | 0/0 | 5068 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0001 | 1/1 | 5052 | 69 | 7 | 18 | 18 | 9 | 15 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0017 | 0/0 | 5075 | 4 | 2 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0023 | 0/0 | 5062 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0030 | 0/0 | 5076 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0031 | 0/0 | 5053 | 2 | 0 | 1 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0045 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0066 | 0/0 | 5047 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0067 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0068 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0069 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0070 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0002t0071 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0005 | 0/0 | 5060 | 16 | 2 | 3 | 8 | 0 | 3 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0007 | 0/0 | 5061 | 11 | 2 | 1 | 7 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0011 | 0/0 | 5062 | 5 | 0 | 0 | 2 | 0 | 3 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0037 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0038 | 0/0 | 5055 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0039 | 0/0 | 5060 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0041 | 0/0 | 5066 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0042 | 0/0 | 5059 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0072 | 0/0 | 5050 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0074 | 0/0 | 5050 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0075 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0004t0081 | 0/0 | 5061 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0005t0004 | 0/0 | 5051 | 27 | 2 | 9 | 10 | 2 | 4 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0005t0032 | 0/0 | 5052 | 2 | 1 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0005t0073 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0005t0076 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0010t0021 | 0/0 | 5057 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0018t0001 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0001c0021t0001 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0001 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0002 | 0/0 | 5058 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0003 | 0/0 | 5048 | 50 | 6 | 8 | 30 | 1 | 5 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0010 | 0/0 | 5069 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0028 | 0/0 | 5047 | 2 | 1 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0029 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0061 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0063 | 0/0 | 5048 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0064 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0003t0065 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0007t0001 | 0/0 | 5052 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0002c0007t0006 | 0/0 | 5059 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0003c0006t0001 | 0/0 | 5052 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0004c0008t0003 | 0/0 | 5048 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0004c0008t0029 | 0/0 | 5050 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0005c0011t0008 | 0/0 | 5068 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0006c0012t0002 | 0/0 | 5058 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0007c0009t0052 | 0/0 | 5075 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0007c0009t0053 | 0/0 | 5074 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0008c0013t0001 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0009c0014t0051 | 0/0 | 5069 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0010c0023t0006 | 0/0 | 5059 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0011c0016t0043 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0012c0017t0034 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0013c0015t0004 | 0/0 | 5051 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0014c0020t0001 | 0/0 | 5052 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0015c0019t0001 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
a0016c0022t0001 | 0/0 | 5052 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | copy fasta | chr19 | 15635897 | 15667825 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0008g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0008g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0008g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0009g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0009g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0009g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0010g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0010g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0010g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0010g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0012g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0012g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0013g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0013g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0013g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0014g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0014g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0014g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0015g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0015g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0015g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0015g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0016g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0016g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0016g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0018g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0018g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0018g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0018g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0019g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0019g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0019g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0020g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0020g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0020g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0022g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0022g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0024g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0024g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0025g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0025g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0026g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0026g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0027g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0027g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0033g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0033g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0035g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0036g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0040g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0044g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0046g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0047g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0048g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0049g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0050g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0054g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0055g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0056g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0057g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0058g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0059g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0060g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0062g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0077g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0078g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0079g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0080g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0082g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0083g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0001t0084g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0378 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0381 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0397 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0403 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0405 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0406 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0407 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0408 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0001g0411 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0017g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0017g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0017g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0017g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0023g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0023g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0030g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0030g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0031g0409 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0031g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0045g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0066g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0067g0386 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0068g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0069g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0070g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0002t0071g0393 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0005g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0011g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0011g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0011g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0011g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0011g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0037g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0038g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0039g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0041g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0042g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0072g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0074g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0075g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0004t0081g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0032g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0032g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0073g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0005t0076g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0010t0021g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0010t0021g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0018t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0001c0021t0001g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0010g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0028g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0028g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0029g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0061g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0063g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0064g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0003t0065g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0007t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0007t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0007t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0002c0007t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0003c0006t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0003c0006t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0003c0006t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0003c0006t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0003c0006t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0004c0008t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0004c0008t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0004c0008t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0004c0008t0029g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0005c0011t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0005c0011t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0006c0012t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0006c0012t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0007c0009t0052g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0007c0009t0053g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0008c0013t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0009c0014t0051g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0010c0023t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0011c0016t0043g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0012c0017t0034g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0013c0015t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0014c0020t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0015c0019t0001g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
a0016c0022t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0246 | EUR | GBR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0347 | EUR | GBR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0364 | EUR | GBR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0350 | EUR | GBR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00280 | hp1 | a0002 | c0003 | t0003 | g0107 | EUR | FIN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0361 | EUR | FIN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0338 | EUR | FIN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00323 | hp2 | a0002 | c0003 | t0010 | g0100 | EUR | FIN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00408 | hp2 | a0002 | c0003 | t0003 | g0134 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00438 | hp2 | a0002 | c0003 | t0003 | g0106 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00558 | hp1 | a0008 | c0013 | t0001 | g0326 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00558 | hp2 | a0001 | c0004 | t0039 | g0051 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00597 | hp1 | a0001 | c0004 | t0005 | g0059 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00597 | hp2 | a0006 | c0012 | t0002 | g0278 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00609 | hp1 | a0002 | c0007 | t0001 | g0110 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00621 | hp1 | a0002 | c0007 | t0001 | g0109 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00621 | hp2 | a0001 | c0001 | t0040 | g0230 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00639 | hp1 | a0001 | c0005 | t0004 | g0041 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0348 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0385 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00642 | hp2 | a0001 | c0005 | t0004 | g0026 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0305 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00673 | hp2 | a0002 | c0007 | t0006 | g0125 | EAS | CHS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00733 | hp1 | a0002 | c0003 | t0003 | g0128 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0339 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00735 | hp2 | a0001 | c0004 | t0005 | g0078 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0362 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG00741 | hp2 | a0001 | c0005 | t0004 | g0021 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01069 | hp2 | a0016 | c0022 | t0001 | g0349 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01070 | hp1 | a0001 | c0005 | t0004 | g0034 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01070 | hp2 | a0001 | c0005 | t0004 | g0002 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01071 | hp2 | a0001 | c0005 | t0004 | g0002 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01074 | hp1 | a0001 | c0002 | t0001 | g0389 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01074 | hp2 | a0002 | c0003 | t0003 | g0141 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01081 | hp1 | a0001 | c0001 | t0015 | g0172 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0397 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0405 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01099 | hp2 | a0001 | c0005 | t0004 | g0028 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0363 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01109 | hp2 | a0001 | c0001 | t0018 | g0194 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01167 | hp1 | a0014 | c0020 | t0001 | g0086 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01168 | hp1 | a0002 | c0003 | t0003 | g0007 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01168 | hp2 | a0001 | c0001 | t0008 | g0202 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01169 | hp1 | a0002 | c0003 | t0003 | g0007 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01169 | hp2 | a0001 | c0001 | t0014 | g0001 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0387 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01175 | hp2 | a0001 | c0004 | t0007 | g0062 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0395 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01192 | hp2 | a0001 | c0005 | t0004 | g0027 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01243 | hp1 | a0001 | c0004 | t0005 | g0079 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01243 | hp2 | a0001 | c0002 | t0031 | g0410 | AMR | PUR | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01255 | hp2 | a0001 | c0001 | t0008 | g0214 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01256 | hp2 | a0001 | c0004 | t0042 | g0004 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01257 | hp2 | a0001 | c0001 | t0008 | g0008 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01258 | hp1 | a0001 | c0001 | t0010 | g0008 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01258 | hp2 | a0001 | c0004 | t0005 | g0004 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0242 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0396 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0353 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01346 | hp2 | a0002 | c0003 | t0003 | g0144 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01358 | hp1 | a0001 | c0001 | t0010 | g0206 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01361 | hp1 | a0002 | c0003 | t0003 | g0089 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01361 | hp2 | a0001 | c0010 | t0021 | g0150 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0403 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01496 | hp2 | a0002 | c0003 | t0003 | g0092 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01515 | hp1 | a0001 | c0005 | t0004 | g0022 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0381 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01516 | hp1 | a0011 | c0016 | t0043 | g0052 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0344 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0345 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01517 | hp2 | a0001 | c0005 | t0004 | g0024 | EUR | IBS | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01891 | hp1 | a0007 | c0009 | t0052 | g0316 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01891 | hp2 | a0002 | c0003 | t0061 | g0130 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01928 | hp1 | a0001 | c0005 | t0004 | g0037 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0302 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0252 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01975 | hp2 | a0002 | c0003 | t0003 | g0105 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01978 | hp1 | a0013 | c0015 | t0004 | g0013 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0394 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0383 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01981 | hp2 | a0010 | c0023 | t0006 | g0303 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02004 | hp2 | a0001 | c0001 | t0008 | g0193 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02015 | hp2 | a0001 | c0001 | t0080 | g0185 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02040 | hp1 | a0001 | c0004 | t0005 | g0070 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02040 | hp2 | a0002 | c0003 | t0003 | g0095 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02055 | hp1 | a0001 | c0001 | t0083 | g0082 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02055 | hp2 | a0001 | c0001 | t0046 | g0180 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02074 | hp2 | a0001 | c0001 | t0006 | g0239 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02080 | hp2 | a0001 | c0004 | t0005 | g0060 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02083 | hp2 | a0001 | c0001 | t0024 | g0269 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02132 | hp2 | a0002 | c0003 | t0003 | g0116 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02135 | hp1 | a0004 | c0008 | t0003 | g0005 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02145 | hp2 | a0002 | c0003 | t0003 | g0145 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02155 | hp1 | a0001 | c0001 | t0058 | g0240 | EAS | CDX | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | CDX | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | CDX | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02257 | hp1 | a0001 | c0001 | t0036 | g0085 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02257 | hp2 | a0001 | c0001 | t0054 | g0201 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0402 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02258 | hp2 | a0005 | c0011 | t0008 | g0177 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0398 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02273 | hp2 | a0001 | c0004 | t0038 | g0073 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02280 | hp1 | a0007 | c0009 | t0053 | g0315 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02280 | hp2 | a0001 | c0001 | t0010 | g0213 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0372 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0399 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PEL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02451 | hp1 | a0001 | c0001 | t0082 | g0081 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02451 | hp2 | a0001 | c0002 | t0017 | g0334 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02572 | hp1 | a0001 | c0002 | t0023 | g0355 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02602 | hp1 | a0001 | c0005 | t0076 | g0031 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02615 | hp1 | a0001 | c0004 | t0005 | g0046 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02615 | hp2 | a0001 | c0002 | t0017 | g0335 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0400 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02622 | hp2 | a0001 | c0002 | t0030 | g0357 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02630 | hp1 | a0001 | c0004 | t0075 | g0038 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02630 | hp2 | a0001 | c0001 | t0062 | g0159 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0191 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02647 | hp2 | a0001 | c0001 | t0084 | g0212 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02683 | hp1 | a0001 | c0004 | t0005 | g0055 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02683 | hp2 | a0001 | c0001 | t0025 | g0175 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02698 | hp1 | a0002 | c0003 | t0002 | g0123 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02698 | hp2 | a0001 | c0001 | t0049 | g0199 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02717 | hp1 | a0001 | c0001 | t0078 | g0165 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02717 | hp2 | a0002 | c0003 | t0003 | g0111 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0204 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02723 | hp2 | a0001 | c0001 | t0035 | g0084 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02735 | hp1 | a0015 | c0019 | t0001 | g0401 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0375 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0411 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0351 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02809 | hp1 | a0001 | c0001 | t0033 | g0189 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02809 | hp2 | a0001 | c0001 | t0055 | g0196 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02818 | hp1 | a0001 | c0005 | t0004 | g0014 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02886 | hp1 | a0001 | c0001 | t0019 | g0171 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02886 | hp2 | a0001 | c0005 | t0004 | g0025 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02895 | hp1 | a0002 | c0003 | t0003 | g0133 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02895 | hp2 | a0001 | c0002 | t0069 | g0336 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02896 | hp1 | a0001 | c0001 | t0033 | g0188 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02897 | hp1 | a0002 | c0003 | t0003 | g0132 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02922 | hp1 | a0001 | c0001 | t0020 | g0207 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02922 | hp2 | a0001 | c0002 | t0068 | g0358 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02965 | hp1 | a0001 | c0004 | t0072 | g0039 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02965 | hp2 | a0001 | c0021 | t0001 | g0404 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02970 | hp1 | a0001 | c0010 | t0021 | g0149 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0187 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0215 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02976 | hp2 | a0001 | c0001 | t0019 | g0181 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0370 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03017 | hp2 | a0002 | c0003 | t0003 | g0140 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03041 | hp1 | a0001 | c0001 | t0056 | g0276 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03041 | hp2 | a0001 | c0001 | t0016 | g0184 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0186 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03098 | hp2 | a0001 | c0002 | t0071 | g0393 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03130 | hp1 | a0001 | c0002 | t0045 | g0377 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03130 | hp2 | a0001 | c0004 | t0074 | g0040 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03139 | hp1 | a0005 | c0011 | t0008 | g0178 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0169 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03195 | hp1 | a0001 | c0001 | t0013 | g0153 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0154 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03209 | hp1 | a0002 | c0003 | t0003 | g0143 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03209 | hp2 | a0001 | c0002 | t0030 | g0333 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03225 | hp1 | a0001 | c0001 | t0020 | g0164 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03225 | hp2 | a0001 | c0002 | t0023 | g0376 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0374 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03453 | hp1 | a0001 | c0001 | t0016 | g0209 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03453 | hp2 | a0001 | c0001 | t0077 | g0412 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03486 | hp1 | a0001 | c0004 | t0007 | g0048 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0192 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03490 | hp1 | a0001 | c0005 | t0004 | g0003 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03490 | hp2 | a0001 | c0004 | t0041 | g0068 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03492 | hp1 | a0001 | c0005 | t0004 | g0003 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03492 | hp2 | a0001 | c0002 | t0067 | g0386 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03516 | hp1 | a0002 | c0003 | t0003 | g0142 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03516 | hp2 | a0001 | c0001 | t0044 | g0083 | AFR | ESN | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03540 | hp1 | a0001 | c0001 | t0013 | g0158 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0337 | AFR | GWD | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0161 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03579 | hp2 | a0001 | c0001 | t0020 | g0174 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0384 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03654 | hp2 | a0001 | c0005 | t0004 | g0042 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03669 | hp1 | a0001 | c0004 | t0007 | g0080 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03669 | hp2 | a0001 | c0002 | t0031 | g0409 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0346 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03704 | hp1 | a0001 | c0004 | t0005 | g0065 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0388 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03710 | hp1 | a0001 | c0004 | t0005 | g0063 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0380 | SAS | PJL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03831 | hp1 | a0002 | c0003 | t0003 | g0117 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03831 | hp2 | a0001 | c0004 | t0011 | g0054 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03834 | hp1 | a0001 | c0004 | t0011 | g0074 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03834 | hp2 | a0001 | c0004 | t0011 | g0064 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0373 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03927 | hp2 | a0001 | c0005 | t0004 | g0029 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03942 | hp1 | a0001 | c0001 | t0010 | g0173 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03942 | hp2 | a0001 | c0002 | t0066 | g0049 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04115 | hp2 | a0002 | c0003 | t0003 | g0122 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0382 | SAS | BEB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04199 | hp2 | a0002 | c0003 | t0003 | g0129 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0407 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0354 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04228 | hp1 | a0001 | c0001 | t0015 | g0176 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0341 | SAS | STU | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0203 | AFR | YRI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18522 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | YRI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CHB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | CHB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | CHB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CHB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18906 | hp1 | a0001 | c0001 | t0018 | g0317 | AFR | YRI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18906 | hp2 | a0001 | c0001 | t0016 | g0210 | AFR | YRI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18939 | hp1 | a0001 | c0001 | t0057 | g0300 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18939 | hp2 | a0002 | c0003 | t0003 | g0113 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0360 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18940 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18941 | hp1 | a0001 | c0001 | t0024 | g0227 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0390 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18945 | hp1 | a0001 | c0005 | t0004 | g0012 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18946 | hp1 | a0001 | c0001 | t0006 | g0221 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18946 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18947 | hp1 | a0003 | c0006 | t0001 | g0323 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18947 | hp2 | a0001 | c0001 | t0048 | g0308 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18948 | hp2 | a0002 | c0003 | t0003 | g0114 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18951 | hp1 | a0002 | c0003 | t0028 | g0093 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18953 | hp1 | a0001 | c0005 | t0073 | g0033 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18954 | hp2 | a0002 | c0003 | t0029 | g0115 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18957 | hp1 | a0002 | c0003 | t0003 | g0088 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18957 | hp2 | a0001 | c0001 | t0027 | g0298 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18959 | hp2 | a0001 | c0004 | t0007 | g0050 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18960 | hp1 | a0001 | c0005 | t0004 | g0032 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18960 | hp2 | a0001 | c0004 | t0011 | g0071 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18961 | hp1 | a0002 | c0003 | t0003 | g0099 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18962 | hp2 | a0002 | c0003 | t0003 | g0005 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18963 | hp1 | a0002 | c0003 | t0003 | g0087 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18965 | hp1 | a0001 | c0005 | t0004 | g0019 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18965 | hp2 | a0003 | c0006 | t0001 | g0324 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18966 | hp2 | a0001 | c0005 | t0032 | g0035 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18968 | hp1 | a0002 | c0003 | t0064 | g0090 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18968 | hp2 | a0001 | c0005 | t0004 | g0015 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18969 | hp1 | a0002 | c0003 | t0003 | g0118 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18969 | hp2 | a0001 | c0001 | t0014 | g0220 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18971 | hp2 | a0001 | c0004 | t0007 | g0053 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18972 | hp1 | a0001 | c0005 | t0004 | g0036 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18972 | hp2 | a0002 | c0007 | t0001 | g0124 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18973 | hp1 | a0002 | c0003 | t0063 | g0091 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18973 | hp2 | a0001 | c0001 | t0026 | g0296 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18978 | hp1 | a0002 | c0003 | t0003 | g0101 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18978 | hp2 | a0001 | c0005 | t0004 | g0017 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18979 | hp2 | a0002 | c0003 | t0003 | g0096 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18981 | hp2 | a0004 | c0008 | t0029 | g0148 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18983 | hp2 | a0002 | c0003 | t0003 | g0098 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18985 | hp1 | a0001 | c0004 | t0037 | g0066 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18986 | hp1 | a0002 | c0003 | t0003 | g0094 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18986 | hp2 | a0001 | c0004 | t0005 | g0067 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18987 | hp1 | a0002 | c0003 | t0065 | g0103 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18987 | hp2 | a0001 | c0004 | t0005 | g0072 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18989 | hp1 | a0001 | c0004 | t0007 | g0057 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18990 | hp1 | a0002 | c0003 | t0003 | g0137 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18990 | hp2 | a0006 | c0012 | t0002 | g0272 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18992 | hp1 | a0001 | c0018 | t0001 | g0371 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18992 | hp2 | a0001 | c0004 | t0007 | g0069 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18994 | hp1 | a0001 | c0005 | t0004 | g0023 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18994 | hp2 | a0001 | c0001 | t0079 | g0281 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18998 | hp1 | a0002 | c0003 | t0003 | g0136 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0366 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18999 | hp1 | a0001 | c0001 | t0014 | g0219 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18999 | hp2 | a0001 | c0001 | t0014 | g0392 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19000 | hp1 | a0001 | c0004 | t0011 | g0077 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19000 | hp2 | a0002 | c0003 | t0003 | g0097 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19001 | hp1 | a0001 | c0001 | t0006 | g0273 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19001 | hp2 | a0002 | c0003 | t0003 | g0006 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19002 | hp1 | a0001 | c0005 | t0004 | g0030 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19002 | hp2 | a0001 | c0004 | t0007 | g0061 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19004 | hp1 | a0003 | c0006 | t0001 | g0325 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0391 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19005 | hp1 | a0001 | c0004 | t0005 | g0056 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19005 | hp2 | a0003 | c0006 | t0001 | g0321 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19007 | hp1 | a0002 | c0003 | t0003 | g0139 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0343 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19009 | hp1 | a0001 | c0001 | t0022 | g0179 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19010 | hp1 | a0001 | c0004 | t0005 | g0076 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19010 | hp2 | a0001 | c0001 | t0025 | g0275 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19011 | hp1 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19011 | hp2 | a0001 | c0001 | t0059 | g0289 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19012 | hp1 | a0002 | c0003 | t0003 | g0102 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19012 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19030 | hp1 | a0001 | c0001 | t0013 | g0152 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19030 | hp2 | a0001 | c0004 | t0007 | g0045 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19043 | hp1 | a0001 | c0001 | t0015 | g0182 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19043 | hp2 | a0001 | c0001 | t0019 | g0318 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19055 | hp1 | a0001 | c0001 | t0060 | g0258 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19056 | hp1 | a0002 | c0003 | t0003 | g0138 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19056 | hp2 | a0002 | c0003 | t0003 | g0104 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19057 | hp2 | a0001 | c0004 | t0005 | g0058 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19058 | hp1 | a0002 | c0003 | t0003 | g0120 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19060 | hp1 | a0001 | c0002 | t0070 | g0379 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19063 | hp1 | a0001 | c0001 | t0050 | g0307 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19063 | hp2 | a0001 | c0001 | t0027 | g0244 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0342 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19065 | hp1 | a0002 | c0003 | t0003 | g0112 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19066 | hp1 | a0001 | c0004 | t0007 | g0170 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19068 | hp1 | a0001 | c0001 | t0022 | g0195 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19070 | hp1 | a0001 | c0005 | t0004 | g0020 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19070 | hp2 | a0001 | c0001 | t0006 | g0238 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0320 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19080 | hp1 | a0001 | c0001 | t0012 | g0198 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0292 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0367 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19083 | hp1 | a0004 | c0008 | t0003 | g0146 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19084 | hp1 | a0001 | c0005 | t0004 | g0016 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19084 | hp2 | a0002 | c0003 | t0003 | g0127 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19085 | hp1 | a0002 | c0003 | t0003 | g0126 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19087 | hp2 | a0001 | c0001 | t0026 | g0288 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19088 | hp1 | a0003 | c0006 | t0001 | g0322 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19090 | hp1 | a0001 | c0004 | t0007 | g0075 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19090 | hp2 | a0001 | c0001 | t0047 | g0010 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19091 | hp1 | a0002 | c0003 | t0003 | g0135 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA19091 | hp2 | a0004 | c0008 | t0003 | g0147 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0197 | AFR | ASW | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA20129 | hp2 | a0012 | c0017 | t0034 | g0043 | AFR | ASW | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA20752 | hp1 | a0002 | c0003 | t0001 | g0131 | EUR | TSI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0408 | EUR | TSI | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0340 | SAS | GIH | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA20905 | hp2 | a0002 | c0003 | t0003 | g0108 | SAS | GIH | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01123 | hp1 | a0001 | c0002 | t0017 | g0359 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG01123 | hp2 | a0001 | c0002 | t0017 | g0356 | AMR | CLM | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02109 | hp1 | a0001 | c0001 | t0018 | g0211 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0200 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02486 | hp1 | a0001 | c0004 | t0005 | g0047 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02486 | hp2 | a0001 | c0001 | t0018 | g0190 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02559 | hp1 | a0001 | c0001 | t0016 | g0162 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG02559 | hp2 | a0009 | c0014 | t0051 | g0208 | AFR | ACB | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0160 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0157 | AFR | MSL | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0151 | AFR | USA | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
HG06807 | hp2 | a0002 | c0003 | t0028 | g0121 | AFR | USA | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA18955 | hp2 | a0002 | c0003 | t0003 | g0119 | EAS | JPT | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA20300 | hp1 | a0001 | c0001 | t0009 | g0205 | AFR | USA | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA20300 | hp2 | a0001 | c0001 | t0015 | g0183 | AFR | USA | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA21309 | hp1 | a0001 | c0005 | t0032 | g0018 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
NA21309 | hp2 | a0001 | c0004 | t0081 | g0044 | AFR | LWK | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0378 | REF | REF | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0406 | REF | REF | CYP4F3_chr19_15635897_15667825 | CYP4F3 | chr19 | 15635897 | 15667825 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15641444
|
G | A | 1 | a0008 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.29G>A | p.Gly10Asp | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/13 | 79/5053 | 29/1563 | 10/520 | chr19 | 15641444 | ||
chr19:15641555
|
G | A | 1 | a0009 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.140G>A | p.Arg47His | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/13 | 190/5053 | 140/1563 | 47/520 | chr19 | 15641555 | ||
chr19:15645729
|
C | T | 1 | a0004 | 4 | HG02135.hp1 NA18981.hp2 NA19083.hp1 others(1): Show |
missense_variant | MODERATE | c.209C>T | p.Ser70Leu | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/13 | 259/5053 | 209/1563 | 70/520 | chr19 | 15645729 | ||
chr19:15645786
|
G | A | 1 | a0007 | 2 | HG01891.hp1 HG02280.hp1 |
missense_variant | MODERATE | c.266G>A | p.Cys89Tyr | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/13 | 316/5053 | 266/1563 | 89/520 | chr19 | 15645786 | ||
chr19:15645818
|
C | T | 1 | a0010 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.298C>T | p.Arg100Cys | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/13 | 348/5053 | 298/1563 | 100/520 | chr19 | 15645818 | ||
chr19:15649236
|
A | G | 1 | a0006 | 2 | HG00597.hp2 NA18990.hp2 |
missense_variant | MODERATE | c.602A>G | p.Asp201Gly | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/13 | 652/5053 | 602/1563 | 201/520 | chr19 | 15649236 | ||
chr19:15650071
|
C | A | 2 | a0002a0004 | 68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
missense_variant | MODERATE | c.806C>A | p.Ala269Asp | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/13 | 856/5053 | 806/1563 | 269/520 | chr19 | 15650071 | ||
chr19:15650073
|
G | A | 1 | a0011 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.808G>A | p.Val270Ile | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/13 | 858/5053 | 808/1563 | 270/520 | chr19 | 15650073 | ||
chr19:15650092
|
G | A | 1 | a0012 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.827G>A | p.Arg276His | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/13 | 877/5053 | 827/1563 | 276/520 | chr19 | 15650092 | ||
chr19:15650164
|
A | T | 1 | a0016 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.899A>T | p.Asp300Val | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/13 | 949/5053 | 899/1563 | 300/520 | chr19 | 15650164 | ||
chr19:15658340
|
G | A | 1 | a0005 | 2 | HG02258.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.1192G>A | p.Val398Ile | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/13 | 1242/5053 | 1192/1563 | 398/520 | chr19 | 15658340 | ||
chr19:15658376
|
G | A | 1 | a0015 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1228G>A | p.Asp410Asn | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/13 | 1278/5053 | 1228/1563 | 410/520 | chr19 | 15658376 | ||
chr19:15659242
|
G | A | 1 | a0003 | 5 | NA18947.hp1 NA18965.hp2 NA19004.hp1 others(2): Show |
missense_variant | MODERATE | c.1420G>A | p.Ala474Thr | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1470/5053 | 1420/1563 | 474/520 | chr19 | 15659242 | ||
chr19:15659249
|
C | A | 1 | a0014 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.1427C>A | p.Ala476Glu | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1477/5053 | 1427/1563 | 476/520 | chr19 | 15659249 | ||
chr19:15659270
|
G | C | 1 | a0009 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1448G>C | p.Gly483Ala | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1498/5053 | 1448/1563 | 483/520 | chr19 | 15659270 | ||
chr19:15659341
|
C | G | 1 | a0013 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1519C>G | p.Arg507Gly | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1569/5053 | 1519/1563 | 507/520 | chr19 | 15659341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15649243
|
G | A | 2 | a0001c0005a0013c0015 | 32 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(29): Show |
synonymous_variant | LOW | c.609G>A | p.Leu203Leu | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/13 | 659/5053 | 609/1563 | 203/520 | chr19 | 15649243 | ||
chr19:15652881
|
G | A | 6 | a0001c0004a0001c0005a0001c0010others(3): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
synonymous_variant | LOW | c.1044G>A | p.Pro348Pro | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/13 | 1094/5053 | 1044/1563 | 348/520 | chr19 | 15652881 | ||
chr19:15652911
|
G | A | 8 | a0001c0001a0002c0003a0004c0008others(5): Show | 246 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(243): Show |
synonymous_variant | LOW | c.1074G>A | p.Val358Val | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/13 | 1124/5053 | 1074/1563 | 358/520 | chr19 | 15652911 | ||
chr19:15652917
|
G | A | 1 | a0001c0018 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.1080G>A | p.Glu360Glu | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/13 | 1130/5053 | 1080/1563 | 360/520 | chr19 | 15652917 | ||
chr19:15658549
|
C | T | 1 | a0001c0010 | 2 | HG01361.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1308C>T | p.Asp436Asp | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/13 | 1358/5053 | 1308/1563 | 436/520 | chr19 | 15658549 | ||
chr19:15659241
|
C | T | 1 | a0001c0010 | 2 | HG01361.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1419C>T | p.Phe473Phe | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1469/5053 | 1419/1563 | 473/520 | chr19 | 15659241 | ||
chr19:15659250
|
G | T | 1 | a0001c0021 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.1428G>T | p.Ala476Ala | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1478/5053 | 1428/1563 | 476/520 | chr19 | 15659250 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15659443
|
G | A | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*58G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 58 | chr19 | 15659443 | |||||
chr19:15659546
|
G | A | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*161G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 161 | chr19 | 15659546 | |||||
chr19:15659561
|
A | G | 4 | a0001c0001t0018a0001c0001t0020a0001c0001t0033others(1): Show | 10 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*176A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 176 | chr19 | 15659561 | |||||
chr19:15659580
|
A | G | 2 | a0001c0001t0082a0001c0001t0083 | 2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*195A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 195 | chr19 | 15659580 | |||||
chr19:15659625
|
T | G | 1 | a0012c0017t0034 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*240T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 240 | chr19 | 15659625 | |||||
chr19:15659626
|
A | G | 1 | a0001c0004t0081 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 241 | chr19 | 15659626 | |||||
chr19:15659635
|
A | G | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*250A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 250 | chr19 | 15659635 | |||||
chr19:15659636
|
T | C | 1 | a0001c0001t0022 | 2 | NA19009.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*251T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 251 | chr19 | 15659636 | |||||
chr19:15659653
|
G | A | 2 | a0001c0001t0035a0001c0001t0036 | 2 | HG02257.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*268G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 268 | chr19 | 15659653 | |||||
chr19:15659665
|
A | T | 1 | a0001c0001t0080 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*280A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 280 | chr19 | 15659665 | |||||
chr19:15659695
|
C | T | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*310C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 310 | chr19 | 15659695 | |||||
chr19:15659742
|
A | G | 1 | a0001c0001t0079 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*357A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 357 | chr19 | 15659742 | |||||
chr19:15659817
|
A | G | 1 | a0001c0001t0078 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 432 | chr19 | 15659817 | |||||
chr19:15659880
|
G | T | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*495G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 495 | chr19 | 15659880 | |||||
chr19:15659890
|
C | T | 9 | a0001c0001t0077a0001c0004t0072a0001c0004t0074others(6): Show | 36 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*505C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 505 | chr19 | 15659890 | |||||
chr19:15659942
|
G | A | 12 | a0001c0001t0040a0001c0004t0005a0001c0004t0007others(9): Show | 41 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*557G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 557 | chr19 | 15659942 | |||||
chr19:15659974
|
G | A | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*589G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 589 | chr19 | 15659974 | |||||
chr19:15660045
|
A | G | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*660A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 660 | chr19 | 15660045 | |||||
chr19:15660214
|
GT | G | 46 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(43): Show | 178 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*833delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 833 | INFO_REALIGN_3_PRIME | chr19 | 15660214 | ||||
chr19:15660279
|
A | G | 1 | a0001c0001t0077 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*894A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 894 | chr19 | 15660279 | |||||
chr19:15660323
|
T | A | 3 | a0001c0001t0009a0001c0001t0013a0001c0001t0044 | 13 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*938T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 938 | chr19 | 15660323 | |||||
chr19:15660377
|
A | G | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*992A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 992 | chr19 | 15660377 | |||||
chr19:15660440
|
T | G | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1055T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1055 | chr19 | 15660440 | |||||
chr19:15660443
|
G | C | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1058G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1058 | chr19 | 15660443 | |||||
chr19:15660447
|
T | C | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1062T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1062 | chr19 | 15660447 | |||||
chr19:15660558
|
C | CTG | 83 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(80): Show | 324 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1174_*1175dupTG | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1176 | INFO_REALIGN_3_PRIME | chr19 | 15660558 | ||||
chr19:15660589
|
G | A | 2 | a0001c0004t0037a0001c0004t0072 | 2 | HG02965.hp1 NA18985.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1204G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1204 | chr19 | 15660589 | |||||
chr19:15660708
|
A | T | 2 | a0001c0001t0027a0001c0001t0060 | 3 | NA18957.hp2 NA19055.hp1 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1323A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1323 | chr19 | 15660708 | |||||
chr19:15660719
|
A | ACTT | 2 | a0001c0002t0023a0001c0002t0045 | 3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1334_*1335insCTT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1335 | chr19 | 15660719 | |||||
chr19:15660719
|
A | AT | 12 | a0001c0001t0003a0001c0001t0035a0001c0001t0036others(9): Show | 65 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1349dupT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1350 | INFO_REALIGN_3_PRIME | chr19 | 15660719 | ||||
chr19:15660719
|
A | ATT | 14 | a0001c0001t0014a0001c0001t0033a0001c0001t0049others(11): Show | 45 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1348_*1349dupTT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1350 | INFO_REALIGN_3_PRIME | chr19 | 15660719 | ||||
chr19:15660719
|
A | ATTT | 40 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(37): Show | 167 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1347_*1349dupTTT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1350 | INFO_REALIGN_3_PRIME | chr19 | 15660719 | ||||
chr19:15660757
|
C | T | 1 | a0002c0003t0063 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1372C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1372 | chr19 | 15660757 | |||||
chr19:15660792
|
C | T | 84 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(81): Show | 326 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*1407C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1407 | chr19 | 15660792 | |||||
chr19:15660803
|
G | A | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1418G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1418 | chr19 | 15660803 | |||||
chr19:15660809
|
T | G | 1 | a0001c0010t0021 | 2 | HG01361.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1424T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1424 | chr19 | 15660809 | |||||
chr19:15660825
|
T | A | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1440T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1440 | chr19 | 15660825 | |||||
chr19:15660839
|
C | T | 2 | a0001c0004t0072a0001c0004t0075 | 2 | HG02630.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1454C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1454 | chr19 | 15660839 | |||||
chr19:15660913
|
C | T | 2 | a0001c0001t0082a0001c0001t0083 | 2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1528C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1528 | chr19 | 15660913 | |||||
chr19:15660922
|
G | A | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1537G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1537 | chr19 | 15660922 | |||||
chr19:15660963
|
C | T | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1578C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1578 | chr19 | 15660963 | |||||
chr19:15660975
|
C | G | 1 | a0001c0001t0077 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1590 | chr19 | 15660975 | |||||
chr19:15660998
|
C | T | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1613C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1613 | chr19 | 15660998 | |||||
chr19:15660999
|
G | T | 12 | a0001c0001t0040a0001c0004t0005a0001c0004t0007others(9): Show | 41 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1614G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1614 | chr19 | 15660999 | |||||
chr19:15661001
|
T | C | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(68): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
3_prime_UTR_variant | MODIFIER | c.*1616T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1616 | chr19 | 15661001 | |||||
chr19:15661161
|
C | T | 68 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(65): Show | 270 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1776C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1776 | chr19 | 15661161 | |||||
chr19:15661168
|
G | A | 80 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(77): Show | 311 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(308): Show |
3_prime_UTR_variant | MODIFIER | c.*1783G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1783 | chr19 | 15661168 | |||||
chr19:15661268
|
A | AAAAAC | 3 | a0001c0001t0009a0001c0001t0044a0001c0002t0070 | 10 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1913_*1917dupCAAA others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1918 | INFO_REALIGN_3_PRIME | chr19 | 15661268 | ||||
chr19:15661268
|
A | AAAAACAA others(3): Show |
1 | a0001c0001t0013 | 4 | HG03195.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1908_*1917dupCAAA others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1918 | INFO_REALIGN_3_PRIME | chr19 | 15661268 | ||||
chr19:15661268
|
AAAAAC | A | 70 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(67): Show | 272 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*1913_*1917delCAAA others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1913 | INFO_REALIGN_3_PRIME | chr19 | 15661268 | ||||
chr19:15661303
|
A | C | 5 | a0001c0001t0009a0001c0001t0013a0001c0001t0044others(2): Show | 16 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1918A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1918 | chr19 | 15661303 | |||||
chr19:15661355
|
C | A | 4 | a0001c0001t0009a0001c0001t0013a0001c0001t0044others(1): Show | 15 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1970C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1970 | chr19 | 15661355 | |||||
chr19:15661356
|
G | A | 5 | a0001c0001t0018a0001c0001t0020a0001c0001t0033others(2): Show | 11 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1971G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 1971 | chr19 | 15661356 | |||||
chr19:15661423
|
T | G | 68 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(65): Show | 270 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*2038T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2038 | chr19 | 15661423 | |||||
chr19:15661567
|
T | A | 58 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(55): Show | 207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2182T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2182 | chr19 | 15661567 | |||||
chr19:15661604
|
G | A | 58 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(55): Show | 207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2219G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2219 | chr19 | 15661604 | |||||
chr19:15661652
|
C | T | 3 | a0001c0004t0072a0001c0004t0074a0001c0004t0075 | 3 | HG02630.hp1 HG02965.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2267C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2267 | chr19 | 15661652 | |||||
chr19:15661689
|
T | A | 57 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(54): Show | 206 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*2304T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2304 | chr19 | 15661689 | |||||
chr19:15661711
|
T | C | 11 | a0001c0001t0040a0001c0004t0005a0001c0004t0007others(8): Show | 40 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2326T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2326 | chr19 | 15661711 | |||||
chr19:15661720
|
C | T | 58 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(55): Show | 207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2335C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2335 | chr19 | 15661720 | |||||
chr19:15661738
|
A | G | 58 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(55): Show | 207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2353A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2353 | chr19 | 15661738 | |||||
chr19:15661754
|
T | A | 58 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(55): Show | 207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2369T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2369 | chr19 | 15661754 | |||||
chr19:15661804
|
T | C | 1 | a0009c0014t0051 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2419T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2419 | chr19 | 15661804 | |||||
chr19:15661906
|
T | C | 11 | a0001c0001t0040a0001c0004t0005a0001c0004t0007others(8): Show | 40 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2521T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2521 | chr19 | 15661906 | |||||
chr19:15661907
|
A | G | 58 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(55): Show | 207 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*2522A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2522 | chr19 | 15661907 | |||||
chr19:15661925
|
T | C | 5 | a0001c0001t0009a0001c0001t0013a0001c0001t0044others(2): Show | 16 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2540T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2540 | chr19 | 15661925 | |||||
chr19:15661928
|
G | A | 56 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(53): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2543G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2543 | chr19 | 15661928 | |||||
chr19:15661971
|
T | G | 1 | a0001c0002t0067 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2586T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2586 | chr19 | 15661971 | |||||
chr19:15662000
|
C | T | 1 | a0002c0003t0065 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2615C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2615 | chr19 | 15662000 | |||||
chr19:15662043
|
T | C | 1 | a0001c0004t0039 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2658T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2658 | chr19 | 15662043 | |||||
chr19:15662262
|
TTC | T | 3 | a0001c0004t0072a0001c0004t0074a0001c0005t0073 | 3 | HG02965.hp1 HG03130.hp2 NA18953.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2886_*2887delTC | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | INFO_REALIGN_3_PRIME | chr19 | 15662262 | ||||
chr19:15662266
|
C | G | 55 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(52): Show | 204 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2881C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2881 | chr19 | 15662266 | |||||
chr19:15662268
|
C | G | 3 | a0001c0004t0072a0001c0004t0074a0001c0005t0073 | 3 | HG02965.hp1 HG03130.hp2 NA18953.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2883C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2883 | chr19 | 15662268 | |||||
chr19:15662270
|
C | CAAAAA | 2 | a0001c0001t0024a0001c0001t0060 | 3 | HG02083.hp2 NA18941.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAA | 12 | a0001c0001t0002a0001c0001t0014a0001c0001t0026others(9): Show | 88 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA | 5 | a0001c0001t0006a0001c0001t0050a0001c0001t0059others(2): Show | 17 | HG00673.hp1 HG00673.hp2 HG01928.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(3): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(1): Show |
4 | a0001c0001t0035a0001c0001t0047a0001c0001t0057others(1): Show | 4 | HG02630.hp2 HG02723.hp2 NA18939.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0056a0001c0001t0083a0001c0002t0023 | 4 | HG02055.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0082 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(7): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0016 | 4 | HG02559.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0012 | 5 | HG02145.hp1 HG02647.hp1 HG03471.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(9): Show |
5 | a0001c0001t0008a0001c0001t0022a0001c0001t0049others(2): Show | 13 | HG01168.hp2 HG01255.hp2 HG01257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(10): Show |
6 | a0001c0001t0010a0001c0001t0020a0001c0001t0033others(3): Show | 14 | HG00323.hp2 HG01258.hp1 HG01358.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(13): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0018a0001c0001t0019 | 7 | HG01109.hp2 HG02109.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0015a0001c0001t0046 | 5 | HG01081.hp1 HG02055.hp2 HG04228.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0054 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(17): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(15): Show |
1 | a0007c0009t0053 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
C | CAAAAAAA others(16): Show |
1 | a0007c0009t0052 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2885_*2886insAAAA others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662270
|
CT | C | 4 | a0001c0004t0075a0001c0005t0004a0001c0005t0076others(1): Show | 30 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2886delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662270 | |||||
chr19:15662271
|
T | A | 50 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(47): Show | 173 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*2886T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2886 | chr19 | 15662271 | |||||
chr19:15662272
|
C | A | 54 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(51): Show | 203 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
3_prime_UTR_variant | MODIFIER | c.*2887C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2887 | chr19 | 15662272 | |||||
chr19:15662272
|
C | CAAAAA | 3 | a0001c0001t0009a0001c0001t0013a0001c0010t0021 | 14 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2903_*2907dupAAAA others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(4): Show |
1 | a0001c0004t0042 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2897_*2907dupAAAA others(7): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(5): Show |
4 | a0001c0004t0005a0001c0004t0038a0001c0004t0039others(1): Show | 19 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2896_*2907dupAAAA others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(6): Show |
2 | a0001c0004t0007a0001c0004t0081 | 12 | HG01175.hp2 HG03486.hp1 HG03669.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2895_*2907dupAAAA others(9): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(7): Show |
2 | a0001c0004t0011a0001c0004t0037 | 6 | HG03831.hp2 HG03834.hp1 HG03834.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2894_*2907dupAAAA others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0040 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2893_*2907dupAAAA others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(15): Show |
2 | a0001c0002t0069a0001c0002t0071 | 2 | HG02895.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2907_*2908insAAAA others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(16): Show |
1 | a0001c0002t0017 | 4 | HG01123.hp1 HG01123.hp2 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2907_*2908insAAAA others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(17): Show |
1 | a0001c0002t0030 | 2 | HG02622.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2907_*2908insAAAA others(20): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
C | CAAAAAAA others(19): Show |
1 | a0001c0002t0068 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2907_*2908insAAAA others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2908 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662272
|
CAA | C | 7 | a0001c0001t0003a0002c0003t0003a0002c0003t0028others(4): Show | 60 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2906_*2907delAA | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2906 | INFO_REALIGN_3_PRIME | chr19 | 15662272 | ||||
chr19:15662354
|
A | G | 1 | a0001c0001t0058 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2969A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 2969 | chr19 | 15662354 | |||||
chr19:15662451
|
TTATAGTA | T | 10 | a0001c0001t0040a0001c0004t0005a0001c0004t0007others(7): Show | 39 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3070_*3076delAGTA others(3): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3070 | INFO_REALIGN_3_PRIME | chr19 | 15662451 | ||||
chr19:15662494
|
A | AT | 68 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(65): Show | 246 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*3115dupT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3116 | INFO_REALIGN_3_PRIME | chr19 | 15662494 | ||||
chr19:15662529
|
C | T | 59 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(56): Show | 208 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*3144C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3144 | chr19 | 15662529 | |||||
chr19:15662559
|
G | T | 9 | a0001c0001t0003a0002c0003t0003a0002c0003t0028others(6): Show | 62 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*3174G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3174 | chr19 | 15662559 | |||||
chr19:15662560
|
T | C | 1 | a0012c0017t0034 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3175T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3175 | chr19 | 15662560 | |||||
chr19:15662617
|
A | G | 5 | a0001c0001t0009a0001c0001t0013a0001c0001t0044others(2): Show | 16 | HG01361.hp2 HG02723.hp1 HG02818.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3232A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3232 | chr19 | 15662617 | |||||
chr19:15662627
|
C | A | 1 | a0001c0001t0055 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3242C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3242 | chr19 | 15662627 | |||||
chr19:15662661
|
A | G | 2 | a0001c0001t0082a0001c0001t0083 | 2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3276A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3276 | chr19 | 15662661 | |||||
chr19:15662722
|
T | C | 10 | a0001c0001t0040a0001c0004t0005a0001c0004t0007others(7): Show | 39 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3337T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 13/13 | 3337 | chr19 | 15662722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15640956
|
G | T | 1 | a0001c0001t0077g0412 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2+11G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 1/12 | chr19 | 15640956 | ||||||
chr19:15641087
|
T | G | 146 | a0001c0001t0035g0084a0001c0001t0036g0085a0001c0001t0044g0083others(143): Show | 150 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-2+142T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 1/12 | chr19 | 15641087 | ||||||
chr19:15641213
|
G | A | 75 | a0001c0002t0066g0049a0001c0004t0005g0004a0001c0004t0005g0046others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.-1-202G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 1/12 | chr19 | 15641213 | ||||||
chr19:15641327
|
C | T | 73 | a0001c0002t0066g0049a0001c0004t0005g0004a0001c0004t0005g0046others(70): Show | 75 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.-1-88C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 1/12 | chr19 | 15641327 | ||||||
chr19:15641687
|
G | A | 1 | a0001c0002t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.198+74G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641687 | ||||||
chr19:15641840
|
C | G | 39 | a0001c0002t0066g0049a0001c0004t0005g0004a0001c0004t0005g0046others(36): Show | 39 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.198+227C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641840 | ||||||
chr19:15641871
|
G | T | 66 | a0002c0003t0001g0131a0002c0003t0002g0123a0002c0003t0003g0005others(63): Show | 68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.198+258G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641871 | ||||||
chr19:15641964
|
T | C | 323 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(320): Show | 328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.198+351T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641964 | ||||||
chr19:15641983
|
T | G | 7 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(4): Show | 7 | HG02818.hp2 HG03195.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+370T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15641983 | ||||||
chr19:15642005
|
G | T | 1 | a0001c0001t0002g0319 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.198+392G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642005 | ||||||
chr19:15642129
|
T | C | 5 | a0001c0001t0012g0160a0001c0001t0012g0161a0001c0001t0012g0163others(2): Show | 5 | HG02145.hp1 HG02559.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+516T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642129 | ||||||
chr19:15642231
|
G | A | 1 | a0001c0002t0001g0320 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.198+618G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642231 | ||||||
chr19:15642460
|
T | C | 1 | a0001c0005t0004g0012 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.198+847T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642460 | ||||||
chr19:15642529
|
C | T | 34 | a0001c0002t0066g0049a0001c0004t0005g0004a0001c0004t0005g0055others(31): Show | 34 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.198+916C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642529 | ||||||
chr19:15642531
|
C | T | 323 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(320): Show | 328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.198+918C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642531 | ||||||
chr19:15642535
|
G | C | 1 | a0001c0001t0062g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.198+922G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642535 | ||||||
chr19:15642602
|
A | T | 1 | a0001c0001t0019g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.198+989A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642602 | ||||||
chr19:15642613
|
T | C | 405 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(402): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.198+1000T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642613 | ||||||
chr19:15642686
|
G | A | 2 | a0002c0003t0003g0087a0002c0003t0003g0088 | 2 | NA18957.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.198+1073G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642686 | ||||||
chr19:15642779
|
G | A | 1 | a0001c0001t0020g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.198+1166G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642779 | ||||||
chr19:15642873
|
A | G | 250 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(247): Show | 253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.198+1260A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642873 | ||||||
chr19:15642884
|
A | AGATG | 5 | a0001c0002t0001g0394a0001c0002t0001g0395a0001c0002t0001g0396others(2): Show | 5 | HG01081.hp2 HG01192.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+1307_198+1310d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15642884 | |||||
chr19:15642884
|
AGATG | A | 12 | a0001c0001t0035g0084a0001c0001t0036g0085a0002c0003t0003g0140others(9): Show | 12 | HG01074.hp2 HG01346.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+1307_198+1310d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15642884 | |||||
chr19:15642884
|
AGATGGAT others(1): Show |
A | 311 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(308): Show | 316 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(313): Show |
intron_variant | MODIFIER | c.198+1303_198+1310d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15642884 | |||||
chr19:15642915
|
T | C | 1 | a0001c0001t0078g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.198+1302T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642915 | ||||||
chr19:15642949
|
G | A | 250 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(247): Show | 253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.198+1336G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642949 | ||||||
chr19:15642979
|
A | C | 1 | a0001c0002t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.198+1366A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642979 | ||||||
chr19:15642992
|
G | A | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | HG00544.hp1 HG02074.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.198+1379G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642992 | ||||||
chr19:15642994
|
T | C | 3 | a0001c0001t0044g0083a0001c0001t0082g0081a0001c0001t0083g0082 | 3 | HG02055.hp1 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.198+1381T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15642994 | ||||||
chr19:15643076
|
AGATG | A | 3 | a0001c0005t0004g0041a0001c0005t0004g0042a0012c0017t0034g0043 | 3 | HG00639.hp1 HG03654.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.198+1485_198+1488d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643076 | |||||
chr19:15643127
|
TTAGA | T | 66 | a0002c0003t0001g0131a0002c0003t0002g0123a0002c0003t0003g0005others(63): Show | 68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.198+1518_198+1521d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643127 | |||||
chr19:15643160
|
AATAG | A | 3 | a0001c0001t0018g0317a0001c0002t0071g0393a0002c0003t0003g0007 | 4 | HG01168.hp1 HG01169.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1556_198+1559d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643160 | |||||
chr19:15643192
|
G | T | 1 | a0001c0001t0077g0412 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.198+1579G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643192 | ||||||
chr19:15643232
|
GGATA | G | 10 | a0001c0001t0012g0160a0001c0001t0012g0161a0001c0001t0012g0163others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+1626_198+1629d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643232 | |||||
chr19:15643239
|
TAGAC | T | 69 | a0001c0004t0072g0039a0001c0004t0074g0040a0001c0004t0075g0038others(66): Show | 71 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.198+1630_198+1633d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643239 | |||||
chr19:15643296
|
C | T | 1 | a0002c0003t0003g0139 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.198+1683C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643296 | ||||||
chr19:15643314
|
TTAGA | T | 82 | a0001c0002t0001g0327a0001c0002t0001g0328a0001c0002t0066g0049others(79): Show | 84 | HG00558.hp1 HG00558.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.198+1718_198+1721d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643314 | |||||
chr19:15643331
|
T | C | 77 | a0001c0001t0010g0169a0001c0001t0012g0160a0001c0001t0012g0161others(74): Show | 79 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.198+1718T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643331 | ||||||
chr19:15643335
|
C | T | 77 | a0001c0001t0010g0169a0001c0001t0012g0160a0001c0001t0012g0161others(74): Show | 79 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.198+1722C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643335 | ||||||
chr19:15643341
|
G | C | 78 | a0001c0001t0010g0169a0001c0001t0012g0160a0001c0001t0012g0161others(75): Show | 80 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.198+1728G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643341 | ||||||
chr19:15643341
|
G | GATAC | 168 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(165): Show | 169 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.198+1744_198+1747d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643341 | |||||
chr19:15643397
|
TATAGGTA others(5): Show |
T | 1 | a0001c0010t0021g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.198+1789_198+1800d others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643397 | |||||
chr19:15643402
|
G | GTAGA | 6 | a0001c0001t0002g0168a0001c0001t0002g0312a0001c0001t0002g0313others(3): Show | 6 | HG01257.hp1 HG02074.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1791_198+1792i others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643402 | |||||
chr19:15643402
|
GTAAA | G | 85 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(82): Show | 86 | HG00597.hp2 HG00673.hp2 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.198+1792_198+1795d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643402 | |||||
chr19:15643402
|
GTAAATAG others(1): Show |
G | 99 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(96): Show | 101 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.198+1792_198+1799d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643402 | |||||
chr19:15643402
|
GTAAATAG others(5): Show |
G | 22 | a0001c0001t0013g0152a0001c0001t0035g0084a0002c0003t0003g0089others(19): Show | 22 | HG00323.hp2 HG00438.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.198+1792_198+1803d others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643402 | |||||
chr19:15643405
|
A | AATAG | 16 | a0001c0002t0001g0011a0001c0002t0001g0380a0001c0002t0001g0381others(13): Show | 17 | HG00642.hp1 HG01074.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.198+1842_198+1845d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | |||||
chr19:15643405
|
A | AATAGATA others(1): Show |
3 | a0001c0001t0014g0392a0001c0002t0001g0391a0001c0002t0001g0411 | 3 | HG02738.hp1 NA18999.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.198+1838_198+1845d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | |||||
chr19:15643405
|
A | G | 38 | a0001c0001t0002g0167a0001c0001t0002g0299a0001c0001t0002g0301others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.198+1792A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643405 | ||||||
chr19:15643405
|
A | T | 4 | a0001c0001t0002g0168a0001c0001t0002g0312a0001c0001t0002g0313others(1): Show | 4 | HG01257.hp1 HG02074.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1792A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643405 | ||||||
chr19:15643405
|
AATAG | A | 80 | a0001c0002t0001g0151a0001c0002t0001g0320a0001c0002t0001g0332others(77): Show | 82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.198+1842_198+1845d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | |||||
chr19:15643405
|
AATAGATA others(1): Show |
A | 9 | a0001c0002t0001g0329a0001c0002t0001g0330a0001c0002t0001g0331others(6): Show | 9 | HG00639.hp1 HG01978.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.198+1838_198+1845d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | |||||
chr19:15643405
|
AATAGATA others(5): Show |
A | 1 | a0001c0004t0081g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.198+1834_198+1845d others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | |||||
chr19:15643405
|
AATAGATA others(9): Show |
A | 1 | a0012c0017t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.198+1830_198+1845d others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15643405 | |||||
chr19:15643409
|
G | T | 17 | a0001c0001t0002g0167a0001c0001t0002g0299a0001c0001t0002g0301others(14): Show | 17 | HG00438.hp1 HG00673.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.198+1796G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643409 | ||||||
chr19:15643413
|
G | T | 40 | a0001c0001t0002g0259a0001c0001t0002g0260a0001c0001t0002g0261others(37): Show | 40 | HG00597.hp2 HG01256.hp1 HG01943.hp1 others(37): Show |
intron_variant | MODIFIER | c.198+1800G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643413 | ||||||
chr19:15643417
|
G | T | 46 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0218others(43): Show | 47 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.198+1804G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643417 | ||||||
chr19:15643433
|
G | C | 1 | a0001c0002t0071g0393 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.198+1820G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643433 | ||||||
chr19:15643461
|
G | C | 2 | a0001c0004t0072g0039a0001c0004t0075g0038 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.198+1848G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643461 | ||||||
chr19:15643465
|
G | A | 10 | a0001c0001t0012g0160a0001c0001t0012g0161a0001c0001t0012g0163others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+1852G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643465 | ||||||
chr19:15643506
|
C | T | 1 | a0001c0002t0001g0378 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.198+1893C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643506 | ||||||
chr19:15643507
|
G | A | 1 | a0001c0001t0006g0217 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.198+1894G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643507 | ||||||
chr19:15643644
|
G | A | 1 | a0001c0004t0037g0066 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.198+2031G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643644 | ||||||
chr19:15643870
|
C | T | 2 | a0001c0001t0035g0084a0001c0001t0036g0085 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.199-1849C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643870 | ||||||
chr19:15643928
|
A | G | 2 | a0001c0002t0001g0330a0001c0002t0001g0331 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.199-1791A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15643928 | ||||||
chr19:15644083
|
A | G | 250 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(247): Show | 253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.199-1636A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644083 | ||||||
chr19:15644098
|
C | T | 4 | a0001c0001t0015g0182a0001c0001t0015g0183a0001c0001t0019g0181others(1): Show | 4 | HG02055.hp2 HG02976.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1621C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644098 | ||||||
chr19:15644163
|
C | T | 2 | a0001c0002t0001g0353a0001c0002t0001g0354 | 2 | HG01346.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.199-1556C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644163 | ||||||
chr19:15644165
|
C | T | 248 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(245): Show | 251 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.199-1554C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644165 | ||||||
chr19:15644299
|
C | A | 1 | a0001c0005t0004g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.199-1420C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644299 | ||||||
chr19:15644302
|
G | A | 248 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(245): Show | 251 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(248): Show |
intron_variant | MODIFIER | c.199-1417G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644302 | ||||||
chr19:15644432
|
C | A | 2 | a0001c0002t0001g0011a0001c0002t0023g0355 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.199-1287C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644432 | ||||||
chr19:15644582
|
G | C | 250 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(247): Show | 253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.199-1137G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644582 | ||||||
chr19:15644592
|
T | TGAG | 250 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(247): Show | 253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.199-1124_199-1122d others(5): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | 15644592 | |||||
chr19:15644632
|
T | C | 323 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(320): Show | 328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.199-1087T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644632 | ||||||
chr19:15644816
|
C | A | 1 | a0001c0004t0005g0067 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.199-903C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644816 | ||||||
chr19:15644819
|
G | A | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-900G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644819 | ||||||
chr19:15644875
|
G | A | 1 | a0001c0021t0001g0404 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.199-844G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15644875 | ||||||
chr19:15645030
|
T | C | 250 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(247): Show | 253 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.199-689T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645030 | ||||||
chr19:15645105
|
C | T | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.199-614C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645105 | ||||||
chr19:15645143
|
G | A | 1 | a0001c0001t0016g0184 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.199-576G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645143 | ||||||
chr19:15645234
|
G | T | 3 | a0001c0001t0044g0083a0001c0001t0082g0081a0001c0001t0083g0082 | 3 | HG02055.hp1 HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.199-485G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645234 | ||||||
chr19:15645354
|
A | C | 323 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(320): Show | 328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.199-365A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645354 | ||||||
chr19:15645673
|
C | T | 2 | a0001c0002t0023g0376a0001c0002t0045g0377 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.199-46C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645673 | ||||||
chr19:15645703
|
G | A | 27 | a0001c0001t0002g0218a0001c0001t0002g0223a0001c0001t0002g0224others(24): Show | 27 | HG00621.hp2 HG02080.hp1 HG02155.hp2 others(24): Show |
intron_variant | MODIFIER | c.199-16G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 2/12 | chr19 | 15645703 | ||||||
chr19:15645947
|
G | A | 2 | a0001c0001t0035g0084a0001c0001t0036g0085 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.343+84G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15645947 | ||||||
chr19:15645952
|
G | A | 110 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(107): Show | 111 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.343+89G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15645952 | ||||||
chr19:15646161
|
T | C | 72 | a0001c0002t0066g0049a0001c0004t0005g0004a0001c0004t0005g0046others(69): Show | 74 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.343+298T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646161 | ||||||
chr19:15646181
|
A | C | 1 | a0001c0002t0001g0352 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.343+318A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646181 | ||||||
chr19:15646346
|
G | A | 39 | a0001c0002t0066g0049a0001c0004t0005g0004a0001c0004t0005g0046others(36): Show | 39 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.343+483G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646346 | ||||||
chr19:15646365
|
C | G | 171 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(168): Show | 172 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.343+502C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646365 | ||||||
chr19:15646405
|
G | A | 1 | a0001c0002t0001g0332 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.343+542G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646405 | ||||||
chr19:15646564
|
G | C | 4 | a0001c0005t0004g0015a0001c0005t0004g0016a0001c0005t0004g0029others(1): Show | 4 | HG03927.hp2 NA18968.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.344-488G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646564 | ||||||
chr19:15646601
|
T | C | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.344-451T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646601 | ||||||
chr19:15646618
|
T | A | 249 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(246): Show | 252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.344-434T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646618 | ||||||
chr19:15646712
|
G | A | 1 | a0001c0001t0044g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.344-340G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646712 | ||||||
chr19:15646718
|
A | G | 249 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(246): Show | 252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.344-334A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646718 | ||||||
chr19:15646833
|
C | T | 247 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(244): Show | 250 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.344-219C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646833 | ||||||
chr19:15646951
|
G | C | 2 | a0001c0001t0035g0084a0001c0001t0036g0085 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.344-101G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646951 | ||||||
chr19:15646988
|
C | A | 1 | a0001c0001t0077g0412 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.344-64C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646988 | ||||||
chr19:15646991
|
C | CA | 10 | a0001c0001t0012g0160a0001c0001t0012g0161a0001c0001t0012g0163others(7): Show | 10 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.344-60dupA | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr19 | 15646991 | |||||
chr19:15646993
|
C | A | 2 | a0001c0001t0027g0298a0001c0001t0060g0258 | 2 | NA18957.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.344-59C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 3/12 | chr19 | 15646993 | ||||||
chr19:15647117
|
T | C | 333 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(330): Show | 338 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(335): Show |
intron_variant | MODIFIER | c.397+12T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 4/12 | chr19 | 15647117 | ||||||
chr19:15647563
|
C | T | 1 | a0001c0001t0077g0412 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.525+239C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647563 | ||||||
chr19:15647587
|
A | C | 323 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(320): Show | 328 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(325): Show |
intron_variant | MODIFIER | c.525+263A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647587 | ||||||
chr19:15647591
|
A | C | 3 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | HG00544.hp1 HG02074.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.525+267A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647591 | ||||||
chr19:15647693
|
C | T | 2 | a0001c0002t0001g0330a0001c0002t0001g0331 | 2 | NA18963.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.525+369C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647693 | ||||||
chr19:15647778
|
G | A | 1 | a0001c0004t0041g0068 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.525+454G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647778 | ||||||
chr19:15647908
|
T | C | 1 | a0001c0005t0004g0002 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.525+584T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647908 | ||||||
chr19:15647936
|
A | C | 7 | a0001c0004t0005g0004a0001c0004t0005g0063a0001c0004t0005g0078others(4): Show | 7 | HG00735.hp2 HG01243.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.525+612A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647936 | ||||||
chr19:15647997
|
A | G | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | NA18985.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.525+673A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15647997 | ||||||
chr19:15648005
|
A | G | 1 | a0002c0003t0003g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.525+681A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648005 | ||||||
chr19:15648007
|
G | A | 1 | a0001c0002t0001g0337 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.525+683G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648007 | ||||||
chr19:15648075
|
A | G | 1 | a0001c0002t0071g0393 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.525+751A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648075 | ||||||
chr19:15648121
|
T | C | 249 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(246): Show | 252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.525+797T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648121 | ||||||
chr19:15648221
|
G | A | 1 | a0012c0017t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.525+897G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648221 | ||||||
chr19:15648393
|
T | C | 1 | a0012c0017t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.526-767T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648393 | ||||||
chr19:15648404
|
G | A | 2 | a0002c0003t0003g0107a0002c0003t0003g0108 | 2 | HG00280.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.526-756G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648404 | ||||||
chr19:15648664
|
G | A | 77 | a0001c0001t0012g0160a0001c0001t0012g0161a0001c0001t0012g0163others(74): Show | 79 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.526-496G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648664 | ||||||
chr19:15648671
|
T | C | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.526-489T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648671 | ||||||
chr19:15648747
|
C | A | 12 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(9): Show | 12 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.526-413C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648747 | ||||||
chr19:15648866
|
C | G | 2 | a0001c0002t0001g0374a0001c0002t0001g0375 | 2 | HG02735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.526-294C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648866 | ||||||
chr19:15648954
|
C | T | 249 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(246): Show | 252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.526-206C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648954 | ||||||
chr19:15648999
|
A | G | 66 | a0002c0003t0001g0131a0002c0003t0002g0123a0002c0003t0003g0005others(63): Show | 68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.526-161A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15648999 | ||||||
chr19:15649018
|
A | G | 249 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(246): Show | 252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.526-142A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15649018 | ||||||
chr19:15649033
|
C | T | 1 | a0001c0004t0081g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.526-127C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 5/12 | chr19 | 15649033 | ||||||
chr19:15649337
|
G | A | 6 | a0001c0001t0010g0169a0001c0001t0015g0182a0001c0001t0015g0183others(3): Show | 6 | HG02055.hp2 HG02886.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.647+56G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/12 | chr19 | 15649337 | ||||||
chr19:15649403
|
C | T | 77 | a0001c0001t0012g0160a0001c0001t0012g0161a0001c0001t0012g0163others(74): Show | 79 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.647+122C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/12 | chr19 | 15649403 | ||||||
chr19:15649767
|
C | T | 249 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(246): Show | 252 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.648-146C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/12 | chr19 | 15649767 | ||||||
chr19:15649912
|
G | A | 1 | a0001c0001t0010g0187 | 1 | HG02970.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.648-1G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 6/12 | chr19 | 15649912 | ||||||
chr19:15650264
|
C | T | 2 | a0001c0001t0082g0081a0001c0001t0083g0082 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.918+81C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650264 | ||||||
chr19:15650274
|
C | A | 1 | a0001c0002t0066g0049 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.918+91C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650274 | ||||||
chr19:15650399
|
C | T | 2 | a0001c0001t0002g0319a0001c0001t0040g0230 | 2 | HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.918+216C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650399 | ||||||
chr19:15650494
|
GTCTTTCT others(4): Show |
G | 1 | a0001c0001t0024g0269 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.918+312_918+322del others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650494 | ||||||
chr19:15650570
|
T | C | 2 | a0001c0002t0001g0332a0001c0002t0070g0379 | 2 | HG00609.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.918+387T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650570 | ||||||
chr19:15650623
|
T | C | 1 | a0001c0001t0002g0231 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.918+440T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650623 | ||||||
chr19:15650655
|
C | CTTCTTT | 11 | a0001c0001t0002g0255a0001c0001t0002g0297a0001c0001t0008g0200others(8): Show | 11 | HG00735.hp1 HG01255.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.918+479_918+484dup others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650655 | |||||
chr19:15650658
|
C | CTTTTTCT others(32): Show |
2 | a0001c0004t0005g0004a0001c0004t0042g0004 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.918+478_918+516dup others(39): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650658 | |||||
chr19:15650660
|
T | C | 3 | a0001c0004t0072g0039a0001c0004t0074g0040a0001c0004t0075g0038 | 3 | HG02630.hp1 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.918+477T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650660 | ||||||
chr19:15650660
|
T | TTTTC | 11 | a0001c0002t0001g0151a0001c0002t0001g0341a0001c0002t0001g0361others(8): Show | 11 | HG00280.hp2 HG00741.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.918+553_918+556dup others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | |||||
chr19:15650660
|
T | TTTTCTTT others(1): Show |
4 | a0001c0002t0001g0380a0001c0005t0004g0029a0001c0005t0004g0032others(1): Show | 4 | HG02602.hp1 HG03710.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+549_918+556dup others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | |||||
chr19:15650660
|
T | TTTTCTTT others(5): Show |
3 | a0001c0002t0001g0400a0001c0005t0032g0018a0015c0019t0001g0401 | 3 | HG02622.hp1 HG02735.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.918+545_918+556dup others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | |||||
chr19:15650660
|
T | TTTTCTTT others(9): Show |
1 | a0001c0005t0004g0017 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.918+541_918+556dup others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | |||||
chr19:15650660
|
T | TTTTCTTT others(17): Show |
1 | a0001c0002t0001g0399 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.918+533_918+556dup others(24): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | |||||
chr19:15650660
|
T | TTTTCTTT others(3): Show |
2 | a0001c0001t0019g0318a0001c0001t0082g0081 | 2 | HG02451.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.918+484_918+485ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | |||||
chr19:15650660
|
TTTTC | T | 17 | a0001c0002t0001g0327a0001c0002t0001g0347a0001c0002t0001g0352others(14): Show | 18 | HG00099.hp2 HG00642.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.918+553_918+556del others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | |||||
chr19:15650660
|
TTTTCTTT others(9): Show |
T | 2 | a0001c0002t0001g0403a0001c0002t0001g0407 | 2 | HG01496.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.918+541_918+556del others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650660 | |||||
chr19:15650664
|
C | CTT | 207 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(204): Show | 210 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.918+483_918+484dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650664 | |||||
chr19:15650664
|
C | CTTTCTTT others(28): Show |
2 | a0001c0004t0005g0067a0001c0004t0005g0070 | 2 | HG02040.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.918+482_918+516dup others(35): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650664 | |||||
chr19:15650666
|
TTC | T | 23 | a0001c0001t0002g0228a0001c0001t0002g0231a0001c0001t0002g0243others(20): Show | 23 | HG00438.hp1 HG01952.hp1 HG02129.hp2 others(20): Show |
intron_variant | MODIFIER | c.918+485_918+486del others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650666 | |||||
chr19:15650668
|
C | CTTTCTTT others(20): Show |
2 | a0001c0004t0007g0045a0001c0004t0007g0062 | 2 | HG01175.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.918+486_918+512dup others(27): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650668 | |||||
chr19:15650668
|
C | CTTTCTTT others(24): Show |
1 | a0001c0004t0005g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.918+486_918+516dup others(31): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650668 | |||||
chr19:15650668
|
C | CTTTCTTT others(40): Show |
1 | a0011c0016t0043g0052 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.918+486_918+532dup others(47): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650668 | |||||
chr19:15650672
|
C | CTTTCTTT others(16): Show |
1 | a0001c0004t0005g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+490_918+512dup others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650672 | |||||
chr19:15650672
|
C | CTTTCTTT others(20): Show |
7 | a0001c0004t0005g0058a0001c0004t0005g0059a0001c0004t0005g0060others(4): Show | 7 | HG00597.hp1 HG02080.hp2 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+490_918+516dup others(27): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650672 | |||||
chr19:15650676
|
C | CTTTCTTT others(12): Show |
1 | a0001c0004t0005g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.918+494_918+512dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650676 | |||||
chr19:15650676
|
C | CTTTCTTT others(14): Show |
1 | a0001c0004t0007g0050 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.918+496_918+516dup others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650676 | |||||
chr19:15650676
|
C | CTTTCTTT others(16): Show |
6 | a0001c0004t0005g0063a0001c0004t0005g0076a0001c0004t0007g0061others(3): Show | 6 | HG03490.hp2 HG03710.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.918+494_918+516dup others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650676 | |||||
chr19:15650676
|
C | CTTTCTTT others(20): Show |
4 | a0001c0002t0066g0049a0001c0004t0005g0055a0001c0004t0005g0065others(1): Show | 4 | HG02683.hp1 HG03704.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+494_918+520dup others(27): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650676 | |||||
chr19:15650680
|
C | CTTTCTTT others(8): Show |
1 | a0001c0004t0007g0048 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.918+498_918+512dup others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650680 | |||||
chr19:15650680
|
C | CTTTCTTT others(12): Show |
5 | a0001c0004t0005g0078a0001c0004t0005g0079a0001c0004t0007g0080others(2): Show | 5 | HG00735.hp2 HG01243.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+498_918+516dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650680 | |||||
chr19:15650682
|
T | C | 1 | a0001c0005t0004g0002 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.918+499T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650682 | ||||||
chr19:15650684
|
C | CTTTCTTT others(8): Show |
1 | a0001c0004t0007g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.918+502_918+516dup others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650684 | |||||
chr19:15650688
|
C | CTTTCTTT others(4): Show |
1 | a0001c0004t0011g0077 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.918+506_918+516dup others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650688 | |||||
chr19:15650688
|
C | CTTTCTTT others(12): Show |
1 | a0001c0004t0007g0053 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.918+506_918+524dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650688 | |||||
chr19:15650698
|
T | TTTTTCTT others(141): Show |
1 | a0001c0004t0011g0074 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.918+516_918+517ins others(148): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650698 | |||||
chr19:15650700
|
C | CTT | 4 | a0001c0001t0008g0008a0001c0001t0008g0202a0001c0001t0010g0008others(1): Show | 4 | HG01168.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+519_918+520dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650700 | |||||
chr19:15650702
|
T | C | 2 | a0001c0001t0010g0206a0001c0001t0015g0172 | 2 | HG01081.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.918+519T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650702 | ||||||
chr19:15650706
|
T | C | 4 | a0001c0001t0008g0008a0001c0001t0008g0202a0001c0001t0010g0008others(1): Show | 4 | HG01168.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+523T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650706 | ||||||
chr19:15650706
|
T | TTTTTCTT others(141): Show |
1 | a0012c0017t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.918+524_918+525ins others(148): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650706 | |||||
chr19:15650709
|
T | TTTCTTTC others(109): Show |
1 | a0001c0002t0067g0386 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.918+544_918+545ins others(116): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650709 | |||||
chr19:15650710
|
T | A | 1 | a0001c0001t0078g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.918+527T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650710 | ||||||
chr19:15650710
|
T | C | 2 | a0001c0001t0010g0173a0001c0001t0082g0081 | 2 | HG02451.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.918+527T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650710 | ||||||
chr19:15650710
|
T | TTCTTTCT others(86): Show |
1 | a0001c0004t0074g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.918+536_918+537ins others(93): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650710 | |||||
chr19:15650710
|
T | TTTTCTC | 8 | a0001c0001t0002g0255a0001c0001t0002g0297a0001c0001t0008g0200others(5): Show | 8 | HG00735.hp1 HG01255.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+528_918+529ins others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650710 | |||||
chr19:15650713
|
T | TTTCTTTC others(123): Show |
1 | a0001c0002t0001g0330 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.918+546_918+547ins others(130): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(127): Show |
1 | a0001c0002t0001g0331 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.918+550_918+551ins others(134): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(123): Show |
1 | a0014c0020t0001g0086 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(130): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(133): Show |
2 | a0001c0002t0001g0329a0001c0002t0001g0338 | 2 | HG00323.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.918+556_918+557ins others(140): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(129): Show |
3 | a0001c0002t0001g0374a0001c0002t0017g0356a0001c0002t0017g0359 | 3 | HG01123.hp1 HG01123.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(136): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(125): Show |
2 | a0001c0002t0001g0339a0001c0002t0001g0360 | 2 | HG00733.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(132): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(121): Show |
7 | a0001c0002t0001g0340a0001c0002t0001g0381a0001c0002t0001g0382others(4): Show | 7 | HG00558.hp1 HG01515.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(117): Show |
1 | a0001c0002t0001g0363 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.918+614_918+615ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(113): Show |
5 | a0001c0002t0001g0346a0001c0002t0001g0353a0001c0002t0001g0367others(2): Show | 5 | HG00621.hp1 HG01346.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+552_918+553ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(109): Show |
11 | a0001c0002t0001g0011a0001c0002t0001g0320a0001c0002t0001g0348others(8): Show | 12 | HG00609.hp1 HG00639.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.918+548_918+549ins others(116): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(105): Show |
10 | a0001c0001t0014g0392a0001c0002t0001g0332a0001c0002t0001g0350others(7): Show | 10 | HG00140.hp2 HG00609.hp2 HG00673.hp2 others(7): Show |
intron_variant | MODIFIER | c.918+544_918+545ins others(112): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTC others(101): Show |
7 | a0001c0002t0001g0328a0001c0002t0001g0337a0001c0002t0001g0387others(4): Show | 7 | HG01175.hp1 HG03540.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+540_918+541ins others(108): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTCTTTT others(97): Show |
1 | a0001c0002t0001g0373 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.918+536_918+537ins others(104): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650713
|
T | TTTTCCTT others(93): Show |
1 | a0001c0002t0001g0389 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.918+532_918+533ins others(100): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650713 | |||||
chr19:15650714
|
T | C | 4 | a0002c0003t0003g0089a0002c0003t0003g0111a0002c0003t0003g0126others(1): Show | 4 | HG01361.hp1 HG02717.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+531T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650714 | ||||||
chr19:15650717
|
T | TTTCTTTC others(145): Show |
1 | a0001c0004t0007g0069 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(152): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | |||||
chr19:15650717
|
T | TTTCTTTC others(117): Show |
1 | a0001c0005t0004g0024 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.918+552_918+553ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | |||||
chr19:15650717
|
T | TTTCTTTC others(105): Show |
1 | a0001c0002t0071g0393 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.918+548_918+549ins others(112): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | |||||
chr19:15650717
|
T | TTTCTTTC others(113): Show |
4 | a0001c0004t0075g0038a0001c0005t0004g0025a0001c0005t0004g0026others(1): Show | 4 | HG00642.hp2 HG01928.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+548_918+549ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | |||||
chr19:15650717
|
T | TTTCTTTC others(105): Show |
1 | a0001c0005t0004g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(112): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | |||||
chr19:15650717
|
T | TTTCTTTC others(109): Show |
3 | a0001c0004t0072g0039a0001c0005t0004g0012a0001c0005t0004g0027 | 3 | HG01192.hp2 HG02965.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.918+544_918+545ins others(116): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650717 | |||||
chr19:15650718
|
T | TTC | 4 | a0001c0001t0008g0008a0001c0001t0008g0202a0001c0001t0010g0008others(1): Show | 4 | HG01168.hp2 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+537_918+538dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTCTCT others(124): Show |
1 | a0002c0003t0003g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.918+538_918+539ins others(131): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTCTCT others(128): Show |
2 | a0002c0003t0003g0112a0002c0003t0003g0129 | 2 | HG04199.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.918+538_918+539ins others(135): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(150): Show |
2 | a0001c0001t0010g0169a0001c0001t0020g0174 | 2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.918+548_918+549ins others(157): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(154): Show |
1 | a0001c0001t0012g0191 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.918+548_918+549ins others(161): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(150): Show |
14 | a0001c0001t0002g0245a0001c0001t0002g0246a0001c0001t0002g0247others(11): Show | 14 | HG00099.hp1 HG02004.hp1 HG03239.hp2 others(11): Show |
intron_variant | MODIFIER | c.918+548_918+549ins others(157): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(147): Show |
2 | a0001c0001t0009g0205a0001c0001t0013g0152 | 2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.918+548_918+549ins others(154): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(153): Show |
1 | a0001c0001t0002g0229 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(160): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(146): Show |
4 | a0001c0001t0018g0317a0001c0001t0019g0171a0001c0001t0025g0175others(1): Show | 4 | HG02559.hp2 HG02683.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+544_918+545ins others(153): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(142): Show |
1 | a0001c0001t0002g0293 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(149): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(150): Show |
1 | a0001c0001t0016g0209 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(157): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(146): Show |
8 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0267others(5): Show | 8 | HG02602.hp2 HG02698.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+544_918+545ins others(153): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTCT others(143): Show |
2 | a0001c0001t0009g0155a0001c0001t0009g0156 | 2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.918+544_918+545ins others(150): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTTT others(142): Show |
12 | a0001c0001t0008g0193a0001c0001t0010g0187a0001c0001t0015g0176others(9): Show | 12 | HG01109.hp2 HG01891.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.918+540_918+541ins others(149): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTTT others(142): Show |
5 | a0001c0001t0002g0251a0001c0001t0002g0253a0001c0001t0002g0295others(2): Show | 5 | HG01358.hp2 HG01952.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+540_918+541ins others(149): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTTT others(139): Show |
2 | a0001c0001t0009g0157a0001c0001t0013g0158 | 2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.918+540_918+541ins others(146): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTCTTTTT others(139): Show |
1 | a0002c0003t0003g0105 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.918+540_918+541ins others(146): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTTTCTCT others(138): Show |
5 | a0001c0001t0008g0197a0001c0001t0015g0182a0001c0001t0015g0183others(2): Show | 5 | HG02809.hp2 HG02976.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+536_918+537ins others(145): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTTTCTCT others(138): Show |
1 | a0001c0001t0002g0254 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.918+536_918+537ins others(145): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTTTCTCT others(135): Show |
1 | a0001c0001t0009g0215 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.918+536_918+537ins others(142): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650718
|
T | TTTTCTCT others(138): Show |
2 | a0005c0011t0008g0177a0005c0011t0008g0178 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.918+536_918+537ins others(145): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650718 | |||||
chr19:15650721
|
T | TTCCTTCC others(91): Show |
1 | a0001c0002t0023g0376 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.918+539_918+540ins others(98): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650721 | |||||
chr19:15650721
|
T | TTTCTTTT others(101): Show |
1 | a0001c0002t0045g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.918+544_918+545ins others(108): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650721 | |||||
chr19:15650722
|
T | C | 1 | a0001c0001t0083g0082 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.918+539T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650722 | ||||||
chr19:15650722
|
T | TTC | 14 | a0001c0001t0002g0255a0001c0001t0002g0297a0001c0001t0008g0200others(11): Show | 14 | HG00735.hp1 HG01255.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.918+541_918+542dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | |||||
chr19:15650722
|
T | TTCTCTCT others(15): Show |
1 | a0001c0010t0021g0150 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.918+542_918+543ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | |||||
chr19:15650722
|
T | TTCTCTCT others(7): Show |
1 | a0001c0005t0004g0028 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.918+542_918+543ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | |||||
chr19:15650722
|
T | TTCTTTCT others(21): Show |
2 | a0001c0001t0027g0244a0001c0001t0050g0307 | 2 | NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.918+548_918+549ins others(28): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | |||||
chr19:15650722
|
T | TTCTTTTT others(17): Show |
2 | a0001c0001t0008g0192a0001c0001t0044g0083 | 2 | HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.918+544_918+545ins others(24): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650722 | |||||
chr19:15650726
|
T | C | 5 | a0002c0003t0003g0005a0002c0003t0003g0113a0002c0003t0063g0091others(2): Show | 5 | HG02135.hp1 NA18939.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+543T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650726 | ||||||
chr19:15650730
|
T | C | 11 | a0001c0001t0012g0160a0002c0003t0003g0087a0002c0003t0003g0088others(8): Show | 11 | HG00408.hp2 HG01496.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.918+547T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650730 | ||||||
chr19:15650734
|
T | C | 8 | a0001c0001t0035g0084a0001c0001t0062g0159a0002c0003t0001g0131others(5): Show | 8 | HG00438.hp2 HG02040.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+551T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650734 | ||||||
chr19:15650736
|
C | T | 6 | a0001c0001t0008g0008a0001c0001t0008g0202a0001c0001t0010g0008others(3): Show | 6 | HG01081.hp1 HG01168.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+553C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650736 | ||||||
chr19:15650737
|
T | C | 6 | a0001c0001t0008g0008a0001c0001t0008g0202a0001c0001t0010g0008others(3): Show | 6 | HG01081.hp1 HG01168.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+554T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | ||||||
chr19:15650737
|
T | TCTCTTTC others(144): Show |
3 | a0001c0001t0078g0165a0002c0003t0003g0007a0002c0003t0003g0097 | 4 | HG01168.hp1 HG01169.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+554_918+555ins others(151): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | ||||||
chr19:15650737
|
T | TCTCTTTC others(148): Show |
12 | a0002c0003t0003g0006a0002c0003t0003g0098a0002c0003t0003g0099others(9): Show | 13 | HG03017.hp2 HG04115.hp2 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.918+554_918+555ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | ||||||
chr19:15650737
|
T | TCTCTTTC others(160): Show |
1 | a0001c0001t0012g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.918+554_918+555ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | ||||||
chr19:15650737
|
T | TCTCTTTC others(164): Show |
1 | a0001c0001t0016g0162 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.918+554_918+555ins others(171): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | ||||||
chr19:15650737
|
T | TCTTTCTT others(11): Show |
1 | a0001c0001t0083g0082 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.918+554_918+555ins others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | ||||||
chr19:15650737
|
T | TCTTTCTT others(132): Show |
2 | a0002c0003t0063g0091a0002c0003t0064g0090 | 2 | NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.918+554_918+555ins others(139): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | ||||||
chr19:15650737
|
T | TCTTTCTT others(136): Show |
3 | a0002c0003t0003g0005a0002c0003t0003g0113a0004c0008t0003g0005 | 3 | HG02135.hp1 NA18939.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.918+554_918+555ins others(143): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650737 | ||||||
chr19:15650738
|
T | C | 29 | a0001c0001t0008g0008a0001c0001t0008g0202a0001c0001t0010g0008others(26): Show | 31 | HG01081.hp1 HG01168.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.918+555T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650738 | ||||||
chr19:15650738
|
T | TCTCTCTT others(156): Show |
1 | a0001c0001t0013g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.918+555_918+556ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650738 | ||||||
chr19:15650738
|
T | TCTTTCTC others(163): Show |
1 | a0001c0001t0002g0299 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.918+555_918+556ins others(170): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650738 | ||||||
chr19:15650738
|
T | TTCTCTCT others(35): Show |
1 | a0001c0010t0021g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(42): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTCTCT others(148): Show |
1 | a0002c0003t0003g0132 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTCTCT others(152): Show |
3 | a0002c0003t0003g0136a0002c0003t0003g0141a0002c0003t0003g0142 | 3 | HG01074.hp2 HG03516.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(159): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTCTCT others(148): Show |
1 | a0002c0003t0010g0100 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTCTCT others(156): Show |
1 | a0002c0003t0003g0143 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTCTCT others(160): Show |
1 | a0001c0001t0002g0270 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTCTTT others(136): Show |
1 | a0002c0003t0003g0114 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(143): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTCTTT others(136): Show |
1 | a0002c0003t0003g0092 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(143): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTCTTT others(140): Show |
8 | a0002c0003t0003g0087a0002c0003t0003g0088a0002c0003t0003g0116others(5): Show | 8 | HG00408.hp2 HG01891.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(147): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTCTC others(151): Show |
1 | a0002c0003t0003g0133 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(158): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(152): Show |
1 | a0002c0003t0003g0101 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(159): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(156): Show |
3 | a0002c0003t0003g0102a0002c0003t0003g0138a0002c0003t0003g0144 | 3 | HG01346.hp2 NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(160): Show |
1 | a0002c0003t0003g0145 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(156): Show |
1 | a0001c0001t0012g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(160): Show |
1 | a0001c0001t0012g0160 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(140): Show |
2 | a0002c0003t0003g0094a0002c0003t0003g0106 | 2 | HG00438.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(147): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(140): Show |
1 | a0002c0003t0001g0131 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(147): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(144): Show |
2 | a0002c0003t0003g0095a0002c0003t0003g0117 | 2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(151): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(148): Show |
1 | a0002c0003t0003g0096 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(148): Show |
1 | a0001c0001t0077g0412 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(156): Show |
1 | a0002c0003t0065g0103 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(163): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(160): Show |
2 | a0002c0003t0003g0104a0004c0008t0029g0148 | 2 | NA18981.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.918+556_918+557ins others(167): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(168): Show |
1 | a0001c0001t0036g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(175): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(164): Show |
1 | a0001c0001t0062g0159 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(171): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(148): Show |
1 | a0001c0001t0035g0084 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(155): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(164): Show |
1 | a0002c0003t0003g0137 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(171): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(178): Show |
1 | a0001c0001t0002g0218 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(185): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(182): Show |
1 | a0001c0001t0002g0232 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(189): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(174): Show |
5 | a0001c0001t0002g0166a0001c0001t0002g0233a0001c0001t0002g0271others(2): Show | 5 | HG00544.hp1 HG02083.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(181): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(41): Show |
1 | a0002c0003t0003g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(48): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(166): Show |
1 | a0001c0001t0003g0234 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(173): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(166): Show |
1 | a0001c0001t0002g0235 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(173): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTCT others(170): Show |
9 | a0001c0001t0002g0009a0001c0001t0002g0168a0001c0001t0002g0256others(6): Show | 10 | HG01069.hp1 HG01071.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(177): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTTT others(162): Show |
2 | a0001c0001t0003g0236a0001c0001t0014g0219 | 2 | HG00544.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.918+556_918+557ins others(169): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTTT others(166): Show |
18 | a0001c0001t0002g0001a0001c0001t0002g0167a0001c0001t0002g0237others(15): Show | 18 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.918+556_918+557ins others(173): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTTT others(170): Show |
1 | a0001c0001t0006g0222 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.918+556_918+557ins others(177): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTCTTTTT others(166): Show |
1 | a0001c0001t0058g0240 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.918+556_918+557ins others(173): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTTCC | 82 | a0001c0001t0002g0229a0001c0001t0002g0245a0001c0001t0002g0246others(79): Show | 82 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.918+564_918+567dup others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTTTCTCT others(33): Show |
1 | a0002c0003t0003g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.918+557_918+558ins others(40): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTTTCTCT others(162): Show |
6 | a0001c0001t0018g0190a0001c0001t0020g0164a0001c0001t0020g0207others(3): Show | 6 | HG02486.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.918+557_918+558ins others(169): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTTTCTCT others(158): Show |
2 | a0001c0001t0002g0231a0001c0001t0002g0241 | 2 | HG00408.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.918+557_918+558ins others(165): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTTTCTCT others(158): Show |
1 | a0001c0001t0002g0243 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.918+557_918+558ins others(165): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTTTCTCT others(162): Show |
31 | a0001c0001t0002g0223a0001c0001t0002g0224a0001c0001t0002g0225others(28): Show | 31 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.918+557_918+558ins others(169): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650738
|
T | TTTTCTCT others(159): Show |
4 | a0001c0001t0009g0186a0001c0001t0009g0203a0001c0001t0009g0204others(1): Show | 4 | HG02723.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+557_918+558ins others(166): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650738 | |||||
chr19:15650751
|
A | T | 5 | a0001c0005t0004g0028a0002c0003t0003g0089a0002c0003t0003g0111others(2): Show | 5 | HG01099.hp2 HG01361.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+568A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650751 | ||||||
chr19:15650754
|
T | C | 5 | a0001c0005t0004g0028a0002c0003t0003g0089a0002c0003t0003g0111others(2): Show | 5 | HG01099.hp2 HG01361.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+571T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650754 | ||||||
chr19:15650755
|
T | A | 5 | a0001c0005t0004g0028a0002c0003t0003g0089a0002c0003t0003g0111others(2): Show | 5 | HG01099.hp2 HG01361.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+572T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650755 | ||||||
chr19:15650776
|
G | A | 2 | a0001c0001t0082g0081a0001c0001t0083g0082 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.918+593G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650776 | ||||||
chr19:15650776
|
G | GTTCTTTC others(12): Show |
4 | a0001c0005t0004g0012a0001c0005t0004g0014a0001c0005t0004g0025others(1): Show | 4 | HG01192.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+596_918+614dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
G | GTTCTTTC others(16): Show |
2 | a0001c0004t0011g0074a0012c0017t0034g0043 | 2 | HG03834.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.918+614_918+615ins others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
G | GTTCTTTC others(132): Show |
1 | a0001c0004t0007g0045 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.918+614_918+615ins others(139): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
G | GTTCTTTC others(136): Show |
1 | a0013c0015t0004g0013 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.918+614_918+615ins others(143): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
G | GTTCTTTC others(140): Show |
17 | a0001c0005t0004g0002a0001c0005t0004g0003a0001c0005t0004g0015others(14): Show | 19 | HG00639.hp1 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.918+614_918+615ins others(147): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
G | GTTCTTTC others(144): Show |
10 | a0001c0004t0005g0046a0001c0004t0005g0047a0001c0004t0005g0072others(7): Show | 10 | HG02486.hp1 HG02615.hp1 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+614_918+615ins others(151): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
G | GTTCTTTC others(203): Show |
1 | a0001c0005t0032g0035 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.918+614_918+615ins others(210): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
G | GTTCTTTC others(144): Show |
1 | a0001c0005t0004g0017 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.918+614_918+615ins others(151): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
G | GTTCTTTC others(32): Show |
1 | a0001c0001t0002g0226 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.918+617_918+618ins others(39): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650776
|
GTTCT | G | 3 | a0001c0002t0001g0011a0001c0002t0001g0369a0001c0002t0023g0355 | 4 | HG02572.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+614_918+617del others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650776 | |||||
chr19:15650779
|
C | CGTTCTTT others(12): Show |
2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.918+596_918+597ins others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(138): Show |
1 | a0001c0001t0054g0201 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.918+596_918+597ins others(145): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(149): Show |
1 | a0001c0001t0010g0213 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.918+596_918+597ins others(156): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(149): Show |
2 | a0001c0001t0012g0198a0001c0001t0019g0318 | 2 | NA19043.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.918+596_918+597ins others(156): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(153): Show |
4 | a0001c0001t0008g0202a0001c0001t0008g0214a0001c0001t0010g0173others(1): Show | 4 | HG01168.hp2 HG01255.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+596_918+597ins others(160): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(157): Show |
4 | a0001c0001t0008g0008a0001c0001t0008g0200a0001c0001t0010g0008others(1): Show | 4 | HG01081.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+596_918+597ins others(164): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(161): Show |
1 | a0001c0001t0022g0179 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.918+596_918+597ins others(168): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(161): Show |
1 | a0001c0001t0010g0206 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.918+596_918+597ins others(168): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(153): Show |
1 | a0001c0001t0008g0192 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.918+596_918+597ins others(160): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(152): Show |
2 | a0001c0001t0027g0244a0001c0001t0050g0307 | 2 | NA19063.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.918+596_918+597ins others(159): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(157): Show |
2 | a0001c0001t0002g0255a0001c0001t0002g0297 | 2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.918+596_918+597ins others(164): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(145): Show |
1 | a0002c0003t0003g0107 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.918+596_918+597ins others(152): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(157): Show |
1 | a0002c0003t0003g0108 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.918+596_918+597ins others(164): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650779
|
C | CGTTCTTT others(28): Show |
2 | a0001c0001t0002g0285a0001c0001t0002g0312 | 2 | HG01257.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.918+596_918+597ins others(35): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650779 | ||||||
chr19:15650780
|
T | C | 25 | a0001c0001t0002g0255a0001c0001t0002g0285a0001c0001t0002g0297others(22): Show | 25 | HG00280.hp1 HG00735.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.918+597T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650780 | ||||||
chr19:15650780
|
T | G | 1 | a0001c0001t0044g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.918+597T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650780 | ||||||
chr19:15650780
|
T | TTTCTTTC others(4): Show |
1 | a0001c0001t0077g0412 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+600_918+610dup others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(8): Show |
33 | a0001c0002t0066g0049a0001c0004t0005g0004a0001c0004t0005g0055others(30): Show | 33 | HG00558.hp2 HG00597.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.918+600_918+614dup others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(113): Show |
4 | a0001c0002t0001g0366a0001c0002t0001g0395a0001c0002t0001g0397others(1): Show | 4 | HG01081.hp2 HG01192.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+614_918+615ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(12): Show |
2 | a0001c0001t0009g0155a0001c0001t0078g0165 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.918+599_918+617dup others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(16): Show |
16 | a0001c0001t0002g0301a0001c0001t0002g0313a0001c0001t0006g0302others(13): Show | 16 | HG01928.hp2 HG01975.hp1 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(20): Show |
8 | a0001c0001t0002g0232a0001c0001t0002g0257a0001c0001t0002g0306others(5): Show | 8 | HG00438.hp1 HG01255.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(27): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(24): Show |
49 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0218others(46): Show | 50 | HG00408.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(31): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(28): Show |
37 | a0001c0001t0002g0225a0001c0001t0002g0235a0001c0001t0002g0242others(34): Show | 37 | HG00099.hp1 HG01261.hp1 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(35): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(32): Show |
24 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(21): Show | 24 | HG00544.hp1 HG00544.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(39): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(36): Show |
5 | a0001c0001t0002g0277a0001c0001t0006g0252a0001c0001t0015g0183others(2): Show | 5 | HG01943.hp1 HG01952.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(43): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(40): Show |
2 | a0001c0001t0002g0228a0001c0001t0015g0176 | 2 | HG04228.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.918+617_918+618ins others(47): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650780
|
T | TTTCTTTC others(44): Show |
1 | a0006c0012t0002g0278 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(51): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650780 | |||||
chr19:15650783
|
C | CTTTCTTT others(6): Show |
1 | a0011c0016t0043g0052 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.918+603_918+615dup others(13): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650783 | |||||
chr19:15650784
|
T | TTTCTTTC others(4): Show |
26 | a0001c0001t0062g0159a0001c0002t0001g0151a0001c0002t0001g0327others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.918+604_918+614dup others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650784 | |||||
chr19:15650784
|
T | TTTCTTTC others(8): Show |
44 | a0001c0001t0016g0162a0002c0003t0001g0131a0002c0003t0003g0005others(41): Show | 45 | HG00408.hp2 HG00438.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.918+603_918+617dup others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650784 | |||||
chr19:15650784
|
T | TTTCTTTC others(12): Show |
1 | a0002c0003t0003g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650784 | |||||
chr19:15650784
|
T | TTTCTTTC others(137): Show |
3 | a0002c0003t0003g0111a0002c0003t0003g0126a0002c0003t0003g0127 | 3 | HG02717.hp2 NA19084.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.918+617_918+618ins others(144): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650784 | |||||
chr19:15650785
|
T | TTCTTTCT others(25): Show |
1 | a0001c0001t0010g0187 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(32): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650785 | |||||
chr19:15650788
|
T | TTTCTTTC others(4): Show |
1 | a0002c0003t0010g0100 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.918+607_918+617dup others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650788 | |||||
chr19:15650793
|
T | TCCTTTCT others(23): Show |
1 | a0001c0001t0012g0163 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.918+610_918+611ins others(30): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650793 | ||||||
chr19:15650793
|
T | TTCTTTCT others(23): Show |
2 | a0001c0001t0012g0160a0001c0001t0012g0161 | 2 | HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.918+617_918+618ins others(30): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650793 | |||||
chr19:15650797
|
T | C | 2 | a0001c0002t0001g0320a0001c0002t0001g0396 | 2 | HG01261.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.918+614T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650797 | ||||||
chr19:15650797
|
T | TTTCTTCT others(157): Show |
1 | a0001c0001t0044g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.918+615_918+616ins others(164): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650797 | |||||
chr19:15650799
|
C | CT | 3 | a0002c0003t0003g0007a0002c0003t0003g0140a0002c0003t0003g0141 | 4 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+617dupT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | |||||
chr19:15650799
|
C | CTTCTT | 5 | a0002c0003t0003g0092a0002c0003t0003g0097a0002c0003t0003g0101others(2): Show | 5 | HG01496.hp2 HG01975.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+617_918+618ins others(5): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | |||||
chr19:15650799
|
C | CTTTCTTT others(35): Show |
1 | a0001c0001t0026g0288 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(42): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | |||||
chr19:15650799
|
C | CTTTCTTT others(39): Show |
1 | a0001c0001t0002g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(46): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | |||||
chr19:15650799
|
C | CTTTCTTT others(43): Show |
1 | a0001c0001t0002g0254 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(50): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | |||||
chr19:15650799
|
C | CTTTCTTT others(47): Show |
1 | a0001c0001t0002g0253 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.918+617_918+618ins others(54): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650799 | |||||
chr19:15650799
|
C | T | 1 | a0001c0004t0007g0069 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.918+616C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650799 | ||||||
chr19:15650801
|
C | T | 7 | a0001c0001t0082g0081a0001c0001t0083g0082a0001c0005t0004g0024others(4): Show | 7 | HG00642.hp2 HG01099.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+618C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650801 | ||||||
chr19:15650803
|
C | T | 9 | a0001c0004t0007g0069a0002c0003t0003g0007a0002c0003t0003g0092others(6): Show | 10 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+620C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650803 | ||||||
chr19:15650805
|
C | CT | 5 | a0002c0003t0003g0092a0002c0003t0003g0097a0002c0003t0003g0101others(2): Show | 5 | HG01496.hp2 HG01975.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+624dupT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650805 | |||||
chr19:15650805
|
C | CTTCT | 12 | a0001c0001t0002g0009a0001c0001t0002g0259a0001c0001t0006g0222others(9): Show | 13 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.918+623_918+626dup others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650805 | |||||
chr19:15650805
|
C | T | 5 | a0001c0001t0082g0081a0001c0001t0083g0082a0001c0005t0004g0028others(2): Show | 5 | HG01099.hp2 HG01361.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+622C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650805 | ||||||
chr19:15650806
|
T | C | 2 | a0001c0005t0004g0028a0002c0003t0003g0089 | 2 | HG01099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.918+623T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650806 | ||||||
chr19:15650806
|
T | TC | 4 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0256others(1): Show | 4 | NA18952.hp2 NA18985.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+623_918+624ins others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650806 | ||||||
chr19:15650806
|
T | TTCTCTCT others(7): Show |
1 | a0001c0001t0002g0250 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.918+628_918+629ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | |||||
chr19:15650806
|
T | TTCTCTTT others(3): Show |
5 | a0001c0001t0016g0162a0001c0001t0035g0084a0002c0003t0003g0135others(2): Show | 5 | HG02559.hp1 HG02723.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+632_918+633ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | |||||
chr19:15650806
|
T | TTCTTTC | 3 | a0001c0001t0009g0205a0001c0001t0013g0153a0001c0002t0001g0216 | 3 | HG02572.hp2 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.918+626_918+627ins others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | |||||
chr19:15650806
|
T | TTCTTTCT others(1): Show |
7 | a0001c0001t0002g0229a0001c0001t0002g0280a0001c0001t0008g0008others(4): Show | 7 | HG01081.hp1 HG01255.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+626_918+627ins others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | |||||
chr19:15650806
|
T | TTCTTTCT others(3): Show |
16 | a0001c0001t0002g0243a0001c0001t0002g0262a0001c0001t0002g0266others(13): Show | 16 | HG01891.hp1 HG02129.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.918+626_918+627ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | |||||
chr19:15650806
|
T | TTCTTTCT others(5): Show |
41 | a0001c0001t0002g0168a0001c0001t0002g0223a0001c0001t0002g0255others(38): Show | 41 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.918+626_918+627ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | |||||
chr19:15650806
|
T | TTTC | 3 | a0001c0001t0012g0161a0001c0001t0012g0163a0001c0002t0001g0320 | 3 | HG02145.hp1 HG03579.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.918+624_918+625ins others(3): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650806 | |||||
chr19:15650807
|
T | C | 2 | a0001c0001t0082g0081a0001c0001t0083g0082 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.918+624T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650807 | ||||||
chr19:15650807
|
TC | T | 9 | a0001c0001t0012g0160a0001c0001t0044g0083a0001c0002t0001g0396others(6): Show | 10 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+625delC | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650807 | ||||||
chr19:15650808
|
C | CTCTT | 9 | a0001c0002t0001g0329a0001c0002t0001g0338a0001c0002t0001g0370others(6): Show | 9 | HG00323.hp1 HG00621.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.918+683_918+686dup others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650808
|
C | CTCTTTCT others(15): Show |
1 | a0002c0003t0003g0144 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.918+632_918+633ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650808
|
C | CTCTTTCT others(1): Show |
5 | a0001c0002t0001g0328a0001c0002t0001g0339a0001c0002t0001g0384others(2): Show | 5 | HG00733.hp2 HG02273.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+679_918+686dup others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650808
|
C | CTCTTTCT others(5): Show |
1 | a0001c0018t0001g0371 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.918+675_918+686dup others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650808
|
C | CTTTCTCT others(9): Show |
20 | a0001c0001t0002g0231a0001c0001t0002g0247a0001c0001t0002g0285others(17): Show | 20 | HG01257.hp1 HG01358.hp1 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.918+626_918+627ins others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650808
|
C | CTTTCTCT others(7): Show |
2 | a0001c0001t0009g0157a0001c0001t0009g0203 | 2 | HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.918+626_918+627ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650808
|
C | T | 7 | a0001c0001t0012g0161a0001c0001t0012g0163a0001c0001t0082g0081others(4): Show | 7 | HG01099.hp2 HG01361.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+625C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650808 | ||||||
chr19:15650808
|
CTCTT | C | 22 | a0001c0001t0014g0392a0001c0002t0001g0011a0001c0002t0001g0330others(19): Show | 23 | HG00609.hp2 HG00673.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.918+683_918+686del others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650808
|
CTCTTTCT others(1): Show |
C | 7 | a0001c0002t0001g0337a0001c0002t0001g0350a0001c0002t0001g0351others(4): Show | 7 | HG00140.hp2 HG01243.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+679_918+686del others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650808
|
CTCTTTCT others(5): Show |
C | 4 | a0001c0002t0001g0388a0001c0002t0001g0402a0001c0002t0001g0411others(1): Show | 4 | HG02258.hp1 HG02735.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+675_918+686del others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650808 | |||||
chr19:15650810
|
C | T | 66 | a0001c0001t0002g0001a0001c0001t0002g0166a0001c0001t0002g0167others(63): Show | 66 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.918+627C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650810 | ||||||
chr19:15650812
|
T | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(93): Show | 97 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.918+629T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650812 | ||||||
chr19:15650812
|
T | TTC | 10 | a0002c0003t0001g0131a0002c0003t0003g0087a0002c0003t0003g0088others(7): Show | 10 | HG02040.hp2 HG02895.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+631_918+632dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650812
|
T | TTCTCTC | 5 | a0001c0001t0062g0159a0001c0001t0077g0412a0002c0003t0003g0122others(2): Show | 5 | HG02630.hp2 HG03453.hp2 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+632_918+633ins others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650812
|
T | TTCTCTCT others(3): Show |
1 | a0001c0001t0036g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.918+632_918+633ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650812
|
T | TTCTTTCT others(98): Show |
1 | a0001c0002t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.918+645_918+646ins others(105): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650812
|
T | TTCTTTCT others(102): Show |
4 | a0001c0002t0001g0364a0001c0002t0001g0365a0001c0002t0001g0375others(1): Show | 4 | HG00140.hp1 HG02735.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+645_918+646ins others(109): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650812
|
T | TTCTTTCT others(94): Show |
1 | a0001c0002t0001g0368 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.918+645_918+646ins others(101): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650812
|
T | TTCTTTCT others(106): Show |
1 | a0001c0002t0001g0341 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.918+649_918+650ins others(113): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650812
|
T | TTCTTTCT others(121): Show |
2 | a0001c0005t0004g0021a0001c0005t0004g0022 | 2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.918+649_918+650ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650812
|
T | TTCTTTCT others(125): Show |
6 | a0001c0004t0005g0058a0001c0004t0005g0065a0001c0004t0005g0076others(3): Show | 6 | HG03704.hp1 HG03831.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+649_918+650ins others(132): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650812 | |||||
chr19:15650814
|
CTT | C | 25 | a0001c0001t0078g0165a0002c0003t0003g0005a0002c0003t0003g0006others(22): Show | 26 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.918+633_918+634del others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650814 | |||||
chr19:15650814
|
CTTTCTT | C | 7 | a0002c0003t0003g0112a0002c0003t0003g0118a0002c0003t0003g0126others(4): Show | 7 | HG04199.hp2 NA18954.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+633_918+638del others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650814 | |||||
chr19:15650816
|
T | C | 90 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(87): Show | 92 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.918+633T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650816 | ||||||
chr19:15650816
|
T | TC | 6 | a0001c0005t0004g0037a0002c0003t0003g0092a0002c0003t0003g0097others(3): Show | 6 | HG01496.hp2 HG01928.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+633_918+634ins others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650816 | ||||||
chr19:15650816
|
T | TTCTTTCT others(102): Show |
1 | a0001c0002t0001g0380 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.918+645_918+646ins others(109): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | |||||
chr19:15650816
|
T | TTCTTTCT others(94): Show |
1 | a0001c0002t0001g0352 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.918+645_918+646ins others(101): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | |||||
chr19:15650816
|
T | TTCTTTCT others(98): Show |
7 | a0001c0002t0001g0342a0001c0002t0001g0343a0001c0002t0001g0347others(4): Show | 7 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+645_918+646ins others(105): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | |||||
chr19:15650816
|
T | TTCTTTCT others(117): Show |
1 | a0001c0004t0005g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.918+645_918+646ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | |||||
chr19:15650816
|
T | TTCTTTCT others(121): Show |
5 | a0001c0004t0005g0055a0001c0004t0005g0063a0001c0004t0005g0070others(2): Show | 5 | HG01175.hp2 HG02040.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+649_918+650ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | |||||
chr19:15650816
|
T | TTCTTTCT others(126): Show |
1 | a0001c0004t0011g0071 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.918+649_918+650ins others(133): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650816 | |||||
chr19:15650819
|
T | A | 1 | a0001c0001t0009g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.918+636T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650819 | ||||||
chr19:15650819
|
T | TC | 2 | a0002c0003t0003g0007a0002c0003t0003g0141 | 3 | HG01074.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.918+636_918+637ins others(1): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650819 | ||||||
chr19:15650820
|
T | C | 94 | a0001c0001t0002g0001a0001c0001t0002g0166a0001c0001t0002g0167others(91): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.918+637T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650820 | ||||||
chr19:15650820
|
T | TTC | 5 | a0002c0003t0003g0092a0002c0003t0003g0097a0002c0003t0003g0101others(2): Show | 5 | HG01496.hp2 HG01975.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+639_918+640dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650820 | |||||
chr19:15650820
|
T | TTCTTTCT others(94): Show |
3 | a0001c0002t0001g0344a0001c0002t0001g0345a0001c0002t0001g0362 | 3 | HG00741.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.918+645_918+646ins others(101): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650820 | |||||
chr19:15650820
|
T | TTCTTTCT others(117): Show |
5 | a0001c0004t0005g0004a0001c0004t0005g0079a0001c0004t0007g0080others(2): Show | 5 | HG01243.hp1 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+649_918+650ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650820 | |||||
chr19:15650820
|
T | TTCTTTCT others(121): Show |
1 | a0011c0016t0043g0052 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.918+649_918+650ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650820 | |||||
chr19:15650822
|
C | T | 1 | a0002c0003t0003g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.918+639C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650822 | ||||||
chr19:15650824
|
T | C | 15 | a0002c0003t0003g0007a0002c0003t0003g0092a0002c0003t0003g0097others(12): Show | 16 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.918+641T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650824 | ||||||
chr19:15650824
|
T | TCTTTCTT others(131): Show |
2 | a0001c0005t0004g0028a0002c0003t0003g0089 | 2 | HG01099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.918+641_918+642ins others(138): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650824 | ||||||
chr19:15650824
|
T | TTCTTCTT others(90): Show |
3 | a0001c0002t0001g0327a0001c0002t0001g0378a0001c0002t0017g0334 | 3 | HG02451.hp2 NA19087.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.918+645_918+646ins others(97): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | |||||
chr19:15650824
|
T | TTCTTCTT others(371): Show |
1 | a0001c0002t0001g0383 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.918+645_918+646ins others(378): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | |||||
chr19:15650824
|
T | TTCTTTCT others(121): Show |
1 | a0001c0004t0005g0056 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.918+649_918+650ins others(128): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | |||||
chr19:15650824
|
T | TTCTTTCT others(113): Show |
2 | a0001c0002t0066g0049a0001c0004t0007g0170 | 2 | HG03942.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.918+649_918+650ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | |||||
chr19:15650824
|
T | TTCTTTCT others(117): Show |
3 | a0001c0004t0005g0059a0001c0004t0005g0067a0001c0004t0037g0066 | 3 | HG00597.hp1 NA18985.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.918+649_918+650ins others(124): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650824 | |||||
chr19:15650826
|
C | T | 2 | a0002c0003t0003g0007a0002c0003t0003g0141 | 3 | HG01074.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.918+643C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650826 | ||||||
chr19:15650828
|
T | C | 6 | a0001c0004t0007g0069a0002c0003t0003g0007a0002c0003t0003g0098others(3): Show | 7 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+645T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650828 | ||||||
chr19:15650828
|
T | TTCTTCTT others(113): Show |
2 | a0001c0004t0005g0060a0001c0004t0039g0051 | 2 | HG00558.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.918+649_918+650ins others(120): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650828 | |||||
chr19:15650830
|
C | T | 2 | a0002c0003t0003g0098a0002c0003t0003g0102 | 2 | NA18983.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.918+647C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650830 | ||||||
chr19:15650832
|
T | C | 4 | a0002c0003t0003g0007a0002c0003t0003g0098a0002c0003t0003g0102others(1): Show | 5 | HG01074.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+649T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650832 | ||||||
chr19:15650836
|
T | C | 2 | a0002c0003t0003g0098a0002c0003t0003g0102 | 2 | NA18983.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.918+653T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650836 | ||||||
chr19:15650836
|
T | TTCTCTCT others(120): Show |
2 | a0001c0001t0082g0081a0001c0001t0083g0082 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.918+656_918+657ins others(127): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650836 | |||||
chr19:15650836
|
T | TTCTTTCT others(75): Show |
2 | a0001c0002t0017g0335a0001c0002t0069g0336 | 2 | HG02615.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.918+666_918+667ins others(82): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650836 | |||||
chr19:15650844
|
T | TTCTCTCT others(8): Show |
1 | a0001c0001t0077g0412 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+664_918+665ins others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650844 | |||||
chr19:15650848
|
T | C | 1 | a0006c0012t0002g0272 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.918+665T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650848 | ||||||
chr19:15650852
|
T | C | 12 | a0001c0001t0002g0231a0001c0001t0002g0285a0001c0001t0002g0290others(9): Show | 12 | HG00597.hp2 HG01257.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.918+669T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650852 | ||||||
chr19:15650856
|
T | C | 45 | a0001c0001t0002g0223a0001c0001t0002g0231a0001c0001t0002g0247others(42): Show | 45 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.918+673T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650856 | ||||||
chr19:15650856
|
T | TTC | 3 | a0001c0001t0009g0155a0001c0001t0010g0173a0001c0001t0013g0153 | 3 | HG02818.hp2 HG03195.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.918+675_918+676dup others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650856 | |||||
chr19:15650856
|
T | TTCTCTCT others(3): Show |
3 | a0001c0001t0002g0235a0001c0001t0002g0262a0001c0001t0002g0266 | 3 | HG02015.hp1 NA18945.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.918+676_918+677ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650856 | |||||
chr19:15650860
|
T | C | 54 | a0001c0001t0002g0223a0001c0001t0002g0231a0001c0001t0002g0235others(51): Show | 54 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.918+677T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650860 | ||||||
chr19:15650860
|
T | TTCTCTC | 3 | a0001c0001t0009g0156a0001c0001t0013g0152a0001c0001t0056g0276 | 3 | HG03041.hp1 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.918+680_918+681ins others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | |||||
chr19:15650860
|
T | TTCTCTCT others(1): Show |
8 | a0001c0001t0008g0193a0001c0001t0008g0200a0001c0001t0012g0191others(5): Show | 8 | HG02004.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+680_918+681ins others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | |||||
chr19:15650860
|
T | TTCTCTCT others(3): Show |
2 | a0001c0001t0019g0318a0007c0009t0053g0315 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.918+680_918+681ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | |||||
chr19:15650860
|
T | TTCTCTCT others(5): Show |
10 | a0001c0001t0002g0255a0001c0001t0002g0287a0001c0001t0002g0291others(7): Show | 10 | HG00735.hp1 NA18953.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.918+680_918+681ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | |||||
chr19:15650860
|
T | TTCTCTCT others(7): Show |
2 | a0001c0001t0002g0225a0001c0001t0002g0245 | 2 | HG04184.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.918+680_918+681ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650860 | |||||
chr19:15650864
|
T | C | 83 | a0001c0001t0002g0223a0001c0001t0002g0225a0001c0001t0002g0231others(80): Show | 83 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.918+681T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650864 | ||||||
chr19:15650864
|
T | TTCTCTCT others(1): Show |
4 | a0001c0001t0009g0186a0001c0001t0009g0204a0001c0001t0009g0215others(1): Show | 4 | HG02723.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+684_918+685ins others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | |||||
chr19:15650864
|
T | TTCTCTCT others(3): Show |
2 | a0001c0001t0013g0154a0001c0001t0013g0158 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.918+684_918+685ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | |||||
chr19:15650864
|
T | TTCTCTCT others(5): Show |
4 | a0001c0001t0008g0197a0001c0001t0010g0213a0001c0001t0015g0182others(1): Show | 4 | HG02280.hp2 HG02886.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+684_918+685ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | |||||
chr19:15650864
|
T | TTCTCTCT others(7): Show |
2 | a0001c0001t0010g0187a0001c0001t0055g0196 | 2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.918+684_918+685ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | |||||
chr19:15650864
|
T | TTCTCTCT others(9): Show |
8 | a0001c0001t0002g0168a0001c0001t0002g0243a0001c0001t0002g0250others(5): Show | 8 | HG02074.hp1 HG02129.hp2 HG04199.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+684_918+685ins others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | |||||
chr19:15650864
|
T | TTCTCTCT others(11): Show |
4 | a0001c0001t0002g0232a0001c0001t0002g0251a0001c0001t0006g0010others(1): Show | 4 | HG01255.hp1 HG01358.hp2 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+684_918+685ins others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | |||||
chr19:15650864
|
T | TTCTCTCT others(13): Show |
2 | a0001c0001t0002g0277a0001c0001t0006g0221 | 2 | HG01943.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.918+684_918+685ins others(20): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | |||||
chr19:15650864
|
T | TTCTCTCT others(15): Show |
1 | a0001c0001t0002g0242 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.918+684_918+685ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650864 | |||||
chr19:15650866
|
C | CTTTCTTT others(5): Show |
4 | a0001c0004t0005g0047a0001c0004t0011g0074a0001c0005t0004g0019others(1): Show | 4 | HG02486.hp1 HG03834.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650866 | |||||
chr19:15650866
|
C | CTTTCTTT others(1): Show |
7 | a0001c0004t0007g0057a0001c0004t0074g0040a0001c0005t0004g0020others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650866 | |||||
chr19:15650866
|
C | CTTTG | 7 | a0001c0004t0005g0046a0001c0004t0007g0045a0001c0004t0007g0048others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650866 | |||||
chr19:15650866
|
C | G | 55 | a0001c0002t0066g0049a0001c0004t0005g0004a0001c0004t0005g0055others(52): Show | 56 | HG00558.hp2 HG00597.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.918+683C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650866 | ||||||
chr19:15650866
|
CTT | C | 5 | a0002c0003t0003g0095a0002c0003t0003g0096a0002c0003t0003g0099others(2): Show | 5 | HG00408.hp2 HG02040.hp2 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+687_918+688del others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650866 | |||||
chr19:15650868
|
T | C | 167 | a0001c0001t0002g0168a0001c0001t0002g0223a0001c0001t0002g0225others(164): Show | 169 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.918+685T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650868 | ||||||
chr19:15650868
|
T | TCTCTCTC others(15): Show |
1 | a0001c0001t0002g0229 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.918+685_918+686ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650868 | ||||||
chr19:15650868
|
T | TCTCTCTC others(10): Show |
1 | a0001c0001t0050g0307 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.918+685_918+686ins others(17): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650868 | ||||||
chr19:15650868
|
T | TCTCTCTC others(12): Show |
1 | a0001c0001t0058g0240 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.918+685_918+686ins others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650868 | ||||||
chr19:15650868
|
T | TTC | 9 | a0001c0001t0012g0160a0001c0001t0012g0161a0001c0001t0012g0163others(6): Show | 9 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(2): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTCTCT others(5): Show |
1 | a0001c0001t0077g0412 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.918+686_918+687ins others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTCTCT others(7): Show |
4 | a0001c0001t0002g0261a0001c0001t0009g0157a0001c0001t0025g0175others(1): Show | 4 | HG02165.hp2 HG02683.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTCTCT others(9): Show |
2 | a0001c0001t0008g0192a0001c0001t0008g0202 | 2 | HG01168.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.918+686_918+687ins others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTCTCT others(11): Show |
1 | a0001c0001t0027g0244 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.918+686_918+687ins others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTCTCT others(13): Show |
28 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0224others(25): Show | 28 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(20): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTCTCT others(15): Show |
20 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0218others(17): Show | 21 | HG00099.hp1 HG00280.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.918+686_918+687ins others(22): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTCTCT others(17): Show |
3 | a0001c0001t0002g0256a0001c0001t0002g0260a0001c0001t0002g0263 | 3 | NA18985.hp2 NA19065.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.918+686_918+687ins others(24): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTCTCT others(19): Show |
1 | a0001c0001t0002g0259 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.918+686_918+687ins others(26): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650868
|
T | TTCTTTCT others(3): Show |
1 | a0001c0010t0021g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.918+686_918+687ins others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15650868 | |||||
chr19:15650870
|
T | C | 245 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(242): Show | 248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.918+687T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650870 | ||||||
chr19:15650883
|
T | TCTCTCTC others(10): Show |
1 | a0001c0001t0002g0293 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.918+700_918+701ins others(17): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650883 | ||||||
chr19:15650883
|
T | TCTCTCTC others(14): Show |
1 | a0001c0001t0002g0270 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.918+700_918+701ins others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650883 | ||||||
chr19:15650883
|
T | TCTCTCTC others(16): Show |
1 | a0001c0001t0006g0222 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.918+700_918+701ins others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650883 | ||||||
chr19:15650897
|
C | T | 7 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(4): Show | 7 | HG02818.hp2 HG03195.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+714C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15650897 | ||||||
chr19:15651099
|
C | T | 8 | a0001c0004t0005g0056a0001c0004t0005g0059a0001c0004t0005g0060others(5): Show | 8 | HG00558.hp2 HG00597.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.918+916C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651099 | ||||||
chr19:15651126
|
GGCCTCCC others(466): Show |
G | 73 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(70): Show | 75 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.918+956_919-958del | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15651126 | |||||
chr19:15651169
|
C | T | 1 | a0001c0001t0084g0212 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.918+986C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651169 | ||||||
chr19:15651268
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.918+1085C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651268 | ||||||
chr19:15651372
|
CT | C | 249 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(246): Show | 252 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.919-1184delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15651372 | |||||
chr19:15651392
|
G | A | 1 | a0001c0002t0001g0370 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.919-1177G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651392 | ||||||
chr19:15651398
|
C | T | 1 | a0002c0003t0003g0118 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.919-1171C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651398 | ||||||
chr19:15651403
|
T | C | 1 | a0001c0001t0044g0083 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.919-1166T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651403 | ||||||
chr19:15651437
|
G | A | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.919-1132G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651437 | ||||||
chr19:15651460
|
T | C | 1 | a0001c0001t0002g0229 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.919-1109T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651460 | ||||||
chr19:15651461
|
G | T | 1 | a0001c0001t0002g0229 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.919-1108G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651461 | ||||||
chr19:15651495
|
C | G | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.919-1074C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651495 | ||||||
chr19:15651529
|
G | A | 1 | a0001c0002t0066g0049 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.919-1040G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651529 | ||||||
chr19:15651563
|
A | G | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.919-1006A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651563 | ||||||
chr19:15651691
|
CTGT | C | 243 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(240): Show | 246 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.919-877_919-875del others(3): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651691 | ||||||
chr19:15651793
|
T | C | 75 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.919-776T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651793 | ||||||
chr19:15651868
|
A | T | 75 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.919-701A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651868 | ||||||
chr19:15651903
|
C | T | 75 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.919-666C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651903 | ||||||
chr19:15651979
|
G | A | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.919-590G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15651979 | ||||||
chr19:15652058
|
T | TAGAGAG | 72 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(69): Show | 74 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.919-500_919-495dup others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15652058 | |||||
chr19:15652058
|
T | TAGAGAGA others(3): Show |
1 | a0012c0017t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.919-504_919-495dup others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15652058 | |||||
chr19:15652128
|
T | A | 75 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.919-441T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15652128 | ||||||
chr19:15652283
|
AT | A | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.919-279delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr19 | 15652283 | |||||
chr19:15652438
|
A | T | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.919-131A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15652438 | ||||||
chr19:15652460
|
C | G | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.919-109C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 7/12 | chr19 | 15652460 | ||||||
chr19:15652710
|
G | A | 5 | a0001c0001t0035g0084a0001c0001t0036g0085a0001c0001t0062g0159others(2): Show | 5 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.985+75G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 8/12 | chr19 | 15652710 | ||||||
chr19:15652767
|
A | C | 75 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.986-56A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 8/12 | chr19 | 15652767 | ||||||
chr19:15652957
|
G | A | 1 | a0001c0002t0001g0384 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.1115+5G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652957 | ||||||
chr19:15652962
|
G | C | 5 | a0003c0006t0001g0321a0003c0006t0001g0322a0003c0006t0001g0323others(2): Show | 5 | NA18947.hp1 NA18965.hp2 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115+10G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652962 | ||||||
chr19:15652965
|
G | A | 33 | a0001c0004t0072g0039a0001c0004t0074g0040a0001c0004t0075g0038others(30): Show | 35 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115+13G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652965 | ||||||
chr19:15652987
|
T | A | 2 | a0001c0001t0009g0155a0001c0001t0009g0156 | 2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1115+35T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652987 | ||||||
chr19:15652988
|
G | C | 75 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1115+36G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15652988 | ||||||
chr19:15653021
|
G | A | 1 | a0001c0001t0078g0165 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1115+69G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653021 | ||||||
chr19:15653119
|
C | G | 75 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.1115+167C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653119 | ||||||
chr19:15653179
|
T | C | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1115+227T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653179 | ||||||
chr19:15653183
|
A | T | 1 | a0002c0003t0003g0144 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1115+231A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653183 | ||||||
chr19:15653188
|
A | T | 73 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(70): Show | 75 | HG00558.hp2 HG00597.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1115+236A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653188 | ||||||
chr19:15653261
|
T | G | 39 | a0001c0004t0005g0004a0001c0004t0005g0046a0001c0004t0005g0047others(36): Show | 39 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1115+309T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653261 | ||||||
chr19:15653295
|
T | G | 1 | a0001c0001t0002g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1115+343T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653295 | ||||||
chr19:15653320
|
C | T | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+368C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653320 | ||||||
chr19:15653321
|
A | G | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+369A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653321 | ||||||
chr19:15653410
|
C | T | 243 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(240): Show | 246 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.1115+458C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653410 | ||||||
chr19:15653506
|
C | A | 34 | a0001c0004t0005g0004a0001c0004t0005g0055a0001c0004t0005g0056others(31): Show | 34 | HG00558.hp2 HG00597.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.1115+554C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653506 | ||||||
chr19:15653557
|
A | C | 2 | a0007c0009t0052g0316a0007c0009t0053g0315 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1115+605A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653557 | ||||||
chr19:15653560
|
C | T | 1 | a0001c0002t0001g0216 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1115+608C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653560 | ||||||
chr19:15653585
|
G | A | 2 | a0005c0011t0008g0177a0005c0011t0008g0178 | 2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1115+633G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653585 | ||||||
chr19:15653593
|
T | C | 1 | a0001c0002t0001g0364 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1115+641T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653593 | ||||||
chr19:15653598
|
G | A | 74 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(71): Show | 76 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1115+646G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653598 | ||||||
chr19:15653663
|
T | C | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1115+711T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653663 | ||||||
chr19:15653704
|
A | G | 321 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(318): Show | 326 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.1115+752A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653704 | ||||||
chr19:15653725
|
AAGAGAGA others(4): Show |
A | 1 | a0001c0018t0001g0371 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1115+784_1115+794d others(13): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653725 | |||||
chr19:15653735
|
G | GGA | 17 | a0001c0002t0001g0320a0001c0002t0001g0345a0001c0002t0001g0347others(14): Show | 17 | HG00099.hp2 HG00140.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.1115+833_1115+834d others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
G | GGAGA | 11 | a0001c0002t0001g0151a0001c0002t0001g0331a0001c0002t0001g0338others(8): Show | 11 | HG00323.hp1 HG00639.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1115+831_1115+834d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
G | GGAGAGA | 9 | a0001c0002t0001g0216a0001c0002t0001g0328a0001c0002t0001g0364others(6): Show | 9 | HG00140.hp1 HG00621.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1115+829_1115+834d others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
G | GGAGAGAG others(1): Show |
3 | a0001c0002t0031g0409a0003c0006t0001g0321a0003c0006t0001g0322 | 3 | HG03669.hp2 NA19005.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1115+827_1115+834d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
G | GGAGAGAG others(3): Show |
1 | a0002c0007t0001g0124 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1115+825_1115+834d others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
G | GGAGAGAG others(7): Show |
2 | a0001c0002t0023g0376a0001c0002t0045g0377 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1115+821_1115+834d others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
G | GGAGAGAG others(9): Show |
1 | a0002c0007t0006g0125 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1115+819_1115+834d others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
G | GGAGAGAG others(19): Show |
1 | a0001c0002t0023g0355 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1115+809_1115+834d others(28): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
GGA | G | 8 | a0001c0002t0001g0332a0001c0002t0001g0340a0001c0002t0001g0352others(5): Show | 8 | HG00609.hp2 HG00639.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115+833_1115+834d others(4): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
GGAGA | G | 27 | a0001c0002t0001g0341a0001c0002t0001g0361a0001c0002t0001g0370others(24): Show | 29 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1115+831_1115+834d others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
GGAGAGA | G | 20 | a0001c0002t0001g0011a0001c0002t0001g0343a0001c0002t0001g0362others(17): Show | 21 | HG00741.hp1 HG01070.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.1115+829_1115+834d others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
GGAGAGAG others(1): Show |
G | 6 | a0001c0001t0006g0010a0001c0001t0047g0010a0001c0002t0001g0365others(3): Show | 6 | HG00558.hp1 HG02622.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1115+827_1115+834d others(10): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
GGAGAGAG others(3): Show |
G | 193 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(190): Show | 194 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(191): Show |
intron_variant | MODIFIER | c.1115+825_1115+834d others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
GGAGAGAG others(5): Show |
G | 2 | a0001c0001t0044g0083a0001c0002t0001g0381 | 2 | HG01515.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1115+823_1115+834d others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
GGAGAGAG others(7): Show |
G | 70 | a0001c0001t0002g0235a0001c0001t0003g0234a0001c0001t0003g0236others(67): Show | 72 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1115+821_1115+834d others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653735
|
GGAGAGAG others(9): Show |
G | 7 | a0001c0001t0035g0084a0001c0001t0036g0085a0001c0001t0062g0159others(4): Show | 7 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1115+819_1115+834d others(18): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653735 | |||||
chr19:15653757
|
A | AGAGT | 12 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(9): Show | 12 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.1115+808_1115+809i others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653757 | |||||
chr19:15653768
|
G | T | 1 | a0001c0005t0004g0028 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1115+816G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653768 | ||||||
chr19:15653773
|
A | AGAGAGAG others(7): Show |
1 | a0001c0004t0075g0038 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1115+834_1115+835i others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653773 | |||||
chr19:15653773
|
A | AGAGAGAG others(5): Show |
1 | a0001c0004t0072g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1115+832_1115+833i others(14): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653773 | |||||
chr19:15653773
|
A | T | 315 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(312): Show | 320 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1115+821A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653773 | ||||||
chr19:15653857
|
T | A | 2 | a0001c0001t0082g0081a0001c0001t0083g0082 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1115+905T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653857 | ||||||
chr19:15653875
|
C | A | 2 | a0001c0001t0035g0084a0001c0001t0036g0085 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1115+923C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15653875 | ||||||
chr19:15653958
|
A | AG | 317 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(314): Show | 322 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.1115+1009dupG | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15653958 | |||||
chr19:15654060
|
C | T | 227 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(224): Show | 230 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.1115+1108C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654060 | ||||||
chr19:15654082
|
CA | C | 75 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(72): Show | 77 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.1115+1131delA | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654082 | ||||||
chr19:15654083
|
A | C | 1 | a0012c0017t0034g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1115+1131A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654083 | ||||||
chr19:15654117
|
G | C | 1 | a0002c0003t0003g0106 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1115+1165G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654117 | ||||||
chr19:15654127
|
T | C | 33 | a0001c0004t0072g0039a0001c0004t0074g0040a0001c0004t0075g0038others(30): Show | 35 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1115+1175T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654127 | ||||||
chr19:15654132
|
C | T | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+1180C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654132 | ||||||
chr19:15654145
|
C | T | 41 | a0001c0001t0040g0230a0001c0001t0077g0412a0001c0004t0005g0004others(38): Show | 41 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1115+1193C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654145 | ||||||
chr19:15654151
|
T | C | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+1199T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654151 | ||||||
chr19:15654203
|
C | T | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1115+1251C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654203 | ||||||
chr19:15654218
|
T | G | 3 | a0001c0001t0008g0193a0001c0001t0008g0214a0001c0001t0049g0199 | 3 | HG01255.hp2 HG02004.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1115+1266T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654218 | ||||||
chr19:15654347
|
C | A | 1 | a0001c0001t0012g0198 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1115+1395C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654347 | ||||||
chr19:15654351
|
T | C | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+1399T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654351 | ||||||
chr19:15654476
|
T | G | 3 | a0001c0002t0023g0355a0001c0002t0023g0376a0001c0002t0045g0377 | 3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1115+1524T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654476 | ||||||
chr19:15654615
|
T | G | 16 | a0001c0001t0002g0166a0001c0001t0002g0167a0001c0001t0002g0168others(13): Show | 16 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.1115+1663T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654615 | ||||||
chr19:15654746
|
A | C | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1115+1794A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654746 | ||||||
chr19:15654789
|
G | A | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1115+1837G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654789 | ||||||
chr19:15654792
|
G | A | 30 | a0001c0005t0004g0002a0001c0005t0004g0003a0001c0005t0004g0012others(27): Show | 32 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1115+1840G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654792 | ||||||
chr19:15654792
|
G | C | 67 | a0001c0001t0003g0234a0001c0001t0003g0236a0001c0001t0035g0084others(64): Show | 69 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1115+1840G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654792 | ||||||
chr19:15654959
|
C | T | 4 | a0001c0001t0009g0203a0001c0001t0009g0204a0001c0001t0009g0205others(1): Show | 4 | HG02723.hp1 HG03516.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115+2007C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654959 | ||||||
chr19:15654998
|
G | A | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1115+2046G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15654998 | ||||||
chr19:15655012
|
C | A | 74 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(71): Show | 76 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1115+2060C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655012 | ||||||
chr19:15655259
|
G | A | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1115+2307G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655259 | ||||||
chr19:15655265
|
T | C | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1115+2313T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655265 | ||||||
chr19:15655277
|
G | A | 1 | a0002c0003t0001g0131 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1115+2325G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655277 | ||||||
chr19:15655344
|
T | A | 1 | a0001c0001t0015g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1115+2392T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655344 | ||||||
chr19:15655403
|
C | T | 13 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(10): Show | 13 | HG02723.hp1 HG02818.hp2 HG02976.hp1 others(10): Show |
intron_variant | MODIFIER | c.1115+2451C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655403 | ||||||
chr19:15655404
|
T | G | 2 | a0001c0001t0035g0084a0001c0001t0036g0085 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1115+2452T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655404 | ||||||
chr19:15655451
|
G | A | 1 | a0001c0001t0015g0172 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1115+2499G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655451 | ||||||
chr19:15655609
|
G | A | 245 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(242): Show | 248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1116-2655G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655609 | ||||||
chr19:15655634
|
A | G | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-2630A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655634 | ||||||
chr19:15655660
|
T | A | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-2604T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655660 | ||||||
chr19:15655705
|
G | A | 30 | a0001c0005t0004g0002a0001c0005t0004g0003a0001c0005t0004g0012others(27): Show | 32 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1116-2559G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655705 | ||||||
chr19:15655723
|
G | A | 1 | a0001c0005t0004g0042 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1116-2541G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655723 | ||||||
chr19:15655728
|
C | T | 1 | a0001c0002t0001g0352 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1116-2536C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655728 | ||||||
chr19:15655765
|
G | A | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-2499G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655765 | ||||||
chr19:15655799
|
A | G | 47 | a0001c0001t0008g0008a0001c0001t0008g0192a0001c0001t0008g0193others(44): Show | 47 | HG00323.hp2 HG01081.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.1116-2465A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655799 | ||||||
chr19:15655811
|
T | A | 1 | a0001c0002t0001g0216 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1116-2453T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655811 | ||||||
chr19:15655841
|
G | A | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-2423G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655841 | ||||||
chr19:15655855
|
C | T | 2 | a0001c0001t0035g0084a0001c0001t0036g0085 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1116-2409C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655855 | ||||||
chr19:15655890
|
T | C | 1 | a0001c0018t0001g0371 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1116-2374T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15655890 | ||||||
chr19:15656056
|
C | T | 174 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(171): Show | 175 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1116-2208C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656056 | ||||||
chr19:15656084
|
C | G | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-2180C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656084 | ||||||
chr19:15656085
|
C | A | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-2179C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656085 | ||||||
chr19:15656117
|
A | G | 1 | a0001c0002t0001g0011 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1116-2147A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656117 | ||||||
chr19:15656205
|
T | G | 3 | a0001c0002t0023g0355a0001c0002t0023g0376a0001c0002t0045g0377 | 3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1116-2059T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656205 | ||||||
chr19:15656241
|
A | G | 161 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(158): Show | 162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1116-2023A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656241 | ||||||
chr19:15656247
|
T | A | 2 | a0001c0001t0002g0277a0001c0001t0002g0301 | 2 | HG01943.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1116-2017T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656247 | ||||||
chr19:15656284
|
GTA | G | 33 | a0001c0004t0072g0039a0001c0004t0074g0040a0001c0004t0075g0038others(30): Show | 35 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1116-1963_1116-196 others(6): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656284 | |||||
chr19:15656284
|
GTATA | G | 285 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(282): Show | 288 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.1116-1965_1116-196 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656284 | |||||
chr19:15656469
|
T | C | 242 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(239): Show | 245 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1116-1795T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656469 | ||||||
chr19:15656469
|
T | TTATC | 4 | a0001c0002t0001g0353a0001c0002t0001g0390a0001c0002t0001g0411others(1): Show | 4 | HG01346.hp1 HG02735.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1743_1116-174 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656469 | |||||
chr19:15656469
|
TTATC | T | 37 | a0001c0002t0001g0011a0001c0002t0001g0151a0001c0002t0001g0327others(34): Show | 38 | HG00280.hp2 HG00323.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1116-1743_1116-174 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656469 | |||||
chr19:15656469
|
TTATCTAT others(1): Show |
T | 25 | a0001c0002t0001g0332a0001c0002t0001g0337a0001c0002t0001g0346others(22): Show | 25 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(22): Show |
intron_variant | MODIFIER | c.1116-1747_1116-174 others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656469 | |||||
chr19:15656469
|
TTATCTAT others(5): Show |
T | 3 | a0001c0002t0001g0351a0001c0002t0001g0352a0001c0021t0001g0404 | 3 | HG02738.hp2 HG02965.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1116-1751_1116-174 others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656469 | |||||
chr19:15656497
|
CTATCTAT others(20): Show |
C | 3 | a0001c0002t0023g0355a0001c0002t0023g0376a0001c0002t0045g0377 | 3 | HG02572.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1116-1765_1116-173 others(31): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656497 | |||||
chr19:15656501
|
C | G | 1 | a0001c0004t0007g0069 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1116-1763C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656501 | ||||||
chr19:15656505
|
CTATCTAT others(12): Show |
C | 4 | a0001c0001t0009g0215a0002c0003t0003g0095a0002c0003t0003g0132others(1): Show | 4 | HG02040.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1757_1116-173 others(23): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656505 | |||||
chr19:15656509
|
C | G | 4 | a0001c0004t0005g0056a0001c0004t0005g0059a0001c0004t0005g0067others(1): Show | 4 | HG00597.hp1 NA18985.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116-1755C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656509 | ||||||
chr19:15656509
|
CTATCTAT others(8): Show |
C | 43 | a0001c0001t0002g0233a0001c0001t0002g0245a0001c0001t0002g0250others(40): Show | 44 | HG00597.hp2 HG00673.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.1116-1753_1116-173 others(19): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656509 | |||||
chr19:15656513
|
C | G | 3 | a0001c0004t0005g0060a0001c0004t0007g0170a0001c0004t0039g0051 | 3 | HG00558.hp2 HG02080.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1116-1751C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656513 | ||||||
chr19:15656513
|
CTATCTAT others(4): Show |
C | 167 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0167others(164): Show | 169 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1116-1749_1116-173 others(15): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656513 | |||||
chr19:15656517
|
CTATCTAT | C | 26 | a0001c0001t0002g0166a0001c0001t0002g0223a0001c0001t0002g0224others(23): Show | 26 | HG00544.hp1 HG01074.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1116-1745_1116-173 others(11): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656517 | |||||
chr19:15656521
|
C | G | 14 | a0001c0001t0040g0230a0001c0004t0005g0046a0001c0004t0005g0047others(11): Show | 14 | HG00621.hp2 HG00735.hp2 HG02273.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116-1743C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656521 | ||||||
chr19:15656521
|
CTAT | C | 9 | a0001c0001t0002g0257a0001c0001t0002g0262a0001c0001t0002g0263others(6): Show | 9 | HG02451.hp2 NA18945.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.1116-1741_1116-173 others(7): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656521 | |||||
chr19:15656524
|
T | TC | 7 | a0001c0001t0002g0264a0001c0001t0002g0284a0001c0001t0025g0175others(4): Show | 7 | HG00597.hp1 HG02165.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(5): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATC | 3 | a0001c0004t0005g0060a0001c0004t0007g0170a0001c0004t0039g0051 | 3 | HG00558.hp2 HG02080.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(9): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATCTA others(6): Show |
13 | a0001c0001t0040g0230a0001c0004t0005g0046a0001c0004t0005g0047others(10): Show | 13 | HG00621.hp2 HG00735.hp2 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(17): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATCTA others(10): Show |
1 | a0001c0004t0072g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1116-1740_1116-173 others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATCTA others(30): Show |
1 | a0001c0005t0004g0012 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1116-1740_1116-173 others(41): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATCTA others(26): Show |
6 | a0001c0005t0004g0015a0001c0005t0004g0016a0001c0005t0004g0019others(3): Show | 6 | HG00741.hp2 HG03654.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(37): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATCTA others(18): Show |
4 | a0001c0004t0005g0070a0001c0004t0005g0079a0001c0010t0021g0149others(1): Show | 4 | HG01243.hp1 HG01361.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATCTA others(22): Show |
13 | a0001c0005t0004g0014a0001c0005t0004g0017a0001c0005t0004g0025others(10): Show | 13 | HG00639.hp1 HG00642.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(33): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATGTA others(14): Show |
6 | a0001c0004t0005g0004a0001c0004t0005g0055a0001c0004t0005g0065others(3): Show | 6 | HG01256.hp2 HG01258.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(25): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TCTATGTA others(18): Show |
12 | a0001c0004t0074g0040a0001c0004t0075g0038a0001c0005t0004g0002others(9): Show | 14 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(29): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TGTATCTA others(10): Show |
11 | a0001c0004t0005g0063a0001c0004t0005g0072a0001c0004t0005g0076others(8): Show | 11 | HG01175.hp2 HG01516.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.1116-1740_1116-173 others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656524
|
T | TGTATCTA others(14): Show |
1 | a0001c0005t0004g0023 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1116-1740_1116-173 others(25): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656524 | ||||||
chr19:15656550
|
C | G | 1 | a0001c0002t0001g0374 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1116-1714C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656550 | ||||||
chr19:15656570
|
A | T | 1 | a0001c0001t0054g0201 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1116-1694A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656570 | ||||||
chr19:15656582
|
A | G | 242 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(239): Show | 245 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1116-1682A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656582 | ||||||
chr19:15656598
|
ATCTG | A | 18 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.1116-1662_1116-165 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656598 | |||||
chr19:15656602
|
GTCTA | G | 74 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(71): Show | 76 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1116-1651_1116-164 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656602 | |||||
chr19:15656626
|
T | A | 4 | a0001c0001t0035g0084a0001c0001t0036g0085a0001c0001t0082g0081others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1638T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656626 | ||||||
chr19:15656728
|
T | C | 77 | a0001c0001t0002g0237a0001c0001t0040g0230a0001c0004t0005g0004others(74): Show | 79 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.1116-1536T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656728 | ||||||
chr19:15656728
|
T | TTATC | 26 | a0001c0001t0002g0277a0001c0002t0001g0332a0001c0002t0001g0338others(23): Show | 26 | HG00323.hp1 HG00609.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.1116-1499_1116-149 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656728 | |||||
chr19:15656728
|
T | TTATCTAT others(1): Show |
48 | a0001c0002t0001g0151a0001c0002t0001g0320a0001c0002t0001g0328others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(45): Show |
intron_variant | MODIFIER | c.1116-1503_1116-149 others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656728 | |||||
chr19:15656728
|
T | TTATCTAT others(5): Show |
12 | a0001c0001t0002g0301a0001c0002t0001g0327a0001c0002t0001g0330others(9): Show | 12 | HG00558.hp1 HG01261.hp2 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1116-1507_1116-149 others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656728 | |||||
chr19:15656728
|
TTATC | T | 4 | a0001c0001t0016g0184a0001c0001t0016g0209a0001c0002t0001g0337others(1): Show | 4 | HG02735.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1499_1116-149 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656728 | |||||
chr19:15656760
|
CT | C | 6 | a0001c0001t0015g0172a0001c0001t0020g0164a0001c0001t0020g0207others(3): Show | 6 | HG01081.hp1 HG01175.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-1503delT | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656760 | ||||||
chr19:15656764
|
CTAT | C | 8 | a0001c0001t0015g0172a0001c0001t0020g0164a0001c0001t0020g0207others(5): Show | 8 | HG01081.hp1 HG01175.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116-1499_1116-149 others(7): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656764 | ||||||
chr19:15656765
|
T | A | 40 | a0001c0001t0002g0274a0001c0001t0008g0008a0001c0001t0008g0193others(37): Show | 42 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1116-1499T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656765 | ||||||
chr19:15656766
|
A | T | 40 | a0001c0001t0002g0274a0001c0001t0008g0008a0001c0001t0008g0193others(37): Show | 42 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1116-1498A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656766 | ||||||
chr19:15656767
|
T | C | 40 | a0001c0001t0002g0274a0001c0001t0008g0008a0001c0001t0008g0193others(37): Show | 42 | HG00597.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1116-1497T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656767 | ||||||
chr19:15656767
|
T | TCTATCAT others(1): Show |
79 | a0001c0001t0002g0009a0001c0001t0002g0166a0001c0001t0002g0167others(76): Show | 81 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1116-1496_1116-149 others(12): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656767 | |||||
chr19:15656767
|
T | TCTATCTA others(5): Show |
111 | a0001c0001t0002g0001a0001c0001t0002g0168a0001c0001t0002g0225others(108): Show | 112 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.1116-1496_1116-149 others(16): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656767 | |||||
chr19:15656767
|
T | TCTATCTA others(9): Show |
14 | a0001c0001t0002g0218a0001c0001t0002g0249a0001c0001t0002g0262others(11): Show | 14 | HG01891.hp1 HG01981.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.1116-1496_1116-149 others(20): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656767 | |||||
chr19:15656780
|
C | A | 257 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(254): Show | 262 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.1116-1484C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656780 | ||||||
chr19:15656780
|
C | CATCA | 61 | a0001c0001t0002g0237a0001c0001t0002g0247a0001c0001t0002g0270others(58): Show | 61 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1116-1482_1116-148 others(8): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15656780 | |||||
chr19:15656797
|
C | T | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-1467C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656797 | ||||||
chr19:15656826
|
A | G | 161 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(158): Show | 162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1116-1438A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656826 | ||||||
chr19:15656841
|
T | A | 3 | a0001c0001t0018g0194a0001c0001t0018g0211a0001c0001t0020g0174 | 3 | HG01109.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1116-1423T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15656841 | ||||||
chr19:15657000
|
C | A | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-1264C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657000 | ||||||
chr19:15657001
|
A | G | 321 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(318): Show | 326 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.1116-1263A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657001 | ||||||
chr19:15657059
|
T | C | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-1205T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657059 | ||||||
chr19:15657096
|
G | T | 2 | a0001c0001t0082g0081a0001c0001t0083g0082 | 2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1116-1168G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657096 | ||||||
chr19:15657099
|
A | G | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-1165A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657099 | ||||||
chr19:15657149
|
A | G | 33 | a0001c0004t0072g0039a0001c0004t0074g0040a0001c0004t0075g0038others(30): Show | 35 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1116-1115A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657149 | ||||||
chr19:15657150
|
T | A | 4 | a0001c0001t0035g0084a0001c0001t0036g0085a0001c0001t0082g0081others(1): Show | 4 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1114T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657150 | ||||||
chr19:15657160
|
G | T | 4 | a0001c0001t0012g0160a0001c0001t0012g0161a0001c0001t0012g0163others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116-1104G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657160 | ||||||
chr19:15657188
|
A | T | 1 | a0011c0016t0043g0052 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1116-1076A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657188 | ||||||
chr19:15657189
|
C | G | 74 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(71): Show | 76 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1116-1075C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657189 | ||||||
chr19:15657197
|
T | A | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-1067T>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657197 | ||||||
chr19:15657363
|
C | A | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-901C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657363 | ||||||
chr19:15657377
|
G | A | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-887G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657377 | ||||||
chr19:15657399
|
C | A | 2 | a0001c0001t0035g0084a0001c0001t0036g0085 | 2 | HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1116-865C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657399 | ||||||
chr19:15657445
|
C | G | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-819C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657445 | ||||||
chr19:15657504
|
G | C | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-760G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657504 | ||||||
chr19:15657573
|
G | A | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-691G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657573 | ||||||
chr19:15657593
|
C | T | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-671C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657593 | ||||||
chr19:15657624
|
C | T | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-640C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657624 | ||||||
chr19:15657660
|
GTAT | G | 242 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(239): Show | 245 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1116-599_1116-597d others(5): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr19 | 15657660 | |||||
chr19:15657689
|
T | C | 76 | a0001c0001t0040g0230a0001c0004t0005g0004a0001c0004t0005g0046others(73): Show | 78 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1116-575T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657689 | ||||||
chr19:15657754
|
G | T | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1116-510G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657754 | ||||||
chr19:15657862
|
T | G | 6 | a0001c0002t0001g0338a0001c0002t0001g0347a0001c0002t0001g0350others(3): Show | 6 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116-402T>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657862 | ||||||
chr19:15657981
|
A | C | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-283A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657981 | ||||||
chr19:15657983
|
C | T | 318 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(315): Show | 323 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.1116-281C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15657983 | ||||||
chr19:15658214
|
G | A | 1 | a0001c0001t0002g0280 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1116-50G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 9/12 | chr19 | 15658214 | ||||||
chr19:15658429
|
G | T | 1 | a0001c0005t0004g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1249+32G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/12 | chr19 | 15658429 | ||||||
chr19:15658443
|
C | A | 242 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(239): Show | 245 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.1249+46C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/12 | chr19 | 15658443 | ||||||
chr19:15658460
|
A | C | 244 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(241): Show | 247 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.1250-31A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 10/12 | chr19 | 15658460 | ||||||
chr19:15658569
|
G | C | 244 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(241): Show | 247 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.1314+14G>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658569 | ||||||
chr19:15658639
|
A | G | 246 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(243): Show | 249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1314+84A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658639 | ||||||
chr19:15658668
|
C | T | 161 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(158): Show | 162 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1315-59C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658668 | ||||||
chr19:15658719
|
G | T | 245 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(242): Show | 248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
splice_region_variant&intron_variant | LOW | c.1315-8G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658719 | ||||||
chr19:15658720
|
C | T | 245 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(242): Show | 248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
splice_region_variant&intron_variant | LOW | c.1315-7C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 11/12 | chr19 | 15658720 | ||||||
chr19:15658815
|
A | G | 321 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(318): Show | 326 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(323): Show |
splice_region_variant&intron_variant | LOW | c.1397+6A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658815 | ||||||
chr19:15658854
|
A | G | 51 | a0001c0001t0008g0008a0001c0001t0008g0192a0001c0001t0008g0193others(48): Show | 51 | HG00323.hp2 HG01081.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.1397+45A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658854 | ||||||
chr19:15658881
|
A | G | 1 | a0001c0001t0006g0273 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1397+72A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658881 | ||||||
chr19:15658897
|
C | G | 3 | a0001c0004t0072g0039a0001c0004t0074g0040a0001c0004t0075g0038 | 3 | HG02630.hp1 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1397+88C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658897 | ||||||
chr19:15658903
|
G | A | 4 | a0001c0001t0008g0192a0001c0001t0012g0191a0001c0001t0016g0184others(1): Show | 4 | HG02647.hp1 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1397+94G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658903 | ||||||
chr19:15658955
|
A | G | 1 | a0001c0005t0076g0031 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1397+146A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658955 | ||||||
chr19:15658956
|
C | T | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1397+147C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658956 | ||||||
chr19:15658965
|
A | G | 246 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(243): Show | 249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1397+156A>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658965 | ||||||
chr19:15658968
|
G | A | 1 | a0001c0004t0081g0044 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1397+159G>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658968 | ||||||
chr19:15658976
|
C | T | 3 | a0001c0004t0007g0062a0001c0004t0038g0073a0011c0016t0043g0052 | 3 | HG01175.hp2 HG01516.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1397+167C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658976 | ||||||
chr19:15658995
|
A | T | 246 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(243): Show | 249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1397+186A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15658995 | ||||||
chr19:15659017
|
C | G | 34 | a0001c0001t0054g0201a0001c0004t0072g0039a0001c0004t0074g0040others(31): Show | 36 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1398-203C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659017 | ||||||
chr19:15659025
|
T | TCTAGGCT others(12): Show |
5 | a0001c0002t0017g0334a0001c0002t0017g0335a0001c0002t0030g0333others(2): Show | 5 | HG02451.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1398-192_1398-174d others(21): Show |
CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 15659025 | |||||
chr19:15659032
|
TG | T | 247 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(244): Show | 250 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1398-182delG | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | 15659032 | |||||
chr19:15659039
|
T | C | 246 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(243): Show | 249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1398-181T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659039 | ||||||
chr19:15659044
|
G | T | 246 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(243): Show | 249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1398-176G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659044 | ||||||
chr19:15659047
|
C | G | 246 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(243): Show | 249 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.1398-173C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659047 | ||||||
chr19:15659062
|
G | T | 245 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(242): Show | 248 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.1398-158G>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659062 | ||||||
chr19:15659092
|
C | T | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1398-128C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659092 | ||||||
chr19:15659100
|
C | G | 2 | a0001c0001t0013g0152a0001c0001t0013g0153 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1398-120C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659100 | ||||||
chr19:15659101
|
C | G | 1 | a0001c0005t0004g0028 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1398-119C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659101 | ||||||
chr19:15659107
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1398-113C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659107 | ||||||
chr19:15659155
|
A | C | 144 | a0001c0001t0003g0234a0001c0001t0003g0236a0001c0001t0035g0084others(141): Show | 148 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1398-65A>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659155 | ||||||
chr19:15659157
|
C | T | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1398-63C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659157 | ||||||
chr19:15659182
|
A | T | 411 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(408): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.1398-38A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659182 | ||||||
chr19:15659183
|
C | T | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1398-37C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659183 | ||||||
chr19:15659202
|
T | C | 278 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(275): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.1398-18T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659202 | ||||||
chr19:15659204
|
C | T | 2 | a0001c0010t0021g0149a0001c0010t0021g0150 | 2 | HG01361.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1398-16C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659204 | ||||||
chr19:15659208
|
T | C | 131 | a0001c0001t0040g0230a0001c0002t0001g0011a0001c0002t0001g0151others(128): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1398-12T>C | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659208 | ||||||
chr19:15659209
|
C | A | 1 | a0001c0002t0023g0355 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1398-11C>A | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659209 | ||||||
chr19:15659210
|
C | T | 131 | a0001c0001t0040g0230a0001c0002t0001g0011a0001c0002t0001g0151others(128): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1398-10C>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659210 | ||||||
chr19:15659216
|
C | G | 16 | a0001c0001t0009g0155a0001c0001t0009g0156a0001c0001t0009g0157others(13): Show | 16 | HG02572.hp1 HG02723.hp1 HG02818.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.1398-4C>G | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659216 | ||||||
chr19:15659217
|
A | T | 278 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0166others(275): Show | 283 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(280): Show |
splice_region_variant&intron_variant | LOW | c.1398-3A>T | CYP4F3 | ENSG00000186529.16 | transcript | ENST00000221307.13 | protein_coding | 12/12 | chr19 | 15659217 |