Item | Value |
---|---|
geneid | 8529 |
ensemblid | ENSG00000186115.13 |
hgncid | 2645 |
symbol | CYP4F2 |
name | cytochrome P450 family 4 subfamily F member 2 |
refseq_nuc | NM_001082.5 |
refseq_prot | NP_001073.3 |
ensembl_nuc | ENST00000221700.11 |
ensembl_prot | ENSP00000221700.3 |
mane_status | MANE Select |
chr | chr19 |
start | 15878023 |
end | 15898074 |
strand | - |
ver | v1.2 |
region | chr19:15878023-15898074 |
region5000 | chr19:15873023-15903074 |
regionname0 | CYP4F2_chr19_15878023_15898074 |
regionname5000 | CYP4F2_chr19_15873023_15903074 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001 | 1/0 | 520 | 244 | 43 | 57 | 110 | 13 | 20 | 79 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0002 | 0/0 | 520 | 57 | 3 | 12 | 30 | 2 | 10 | 26 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0003 | 0/1 | 520 | 29 | 2 | 7 | 9 | 3 | 7 | 6 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004 | 0/0 | 520 | 21 | 20 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0005 | 0/0 | 520 | 14 | 12 | 1 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0006 | 0/0 | 520 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0007 | 0/0 | 520 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0008 | 0/0 | 520 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0009 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0010 | 0/0 | 520 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0011 | 0/0 | 520 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0012 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0001 | 1/0 | 1563 | 146 | 22 | 30 | 73 | 6 | 14 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0002 | 0/0 | 1563 | 78 | 7 | 24 | 34 | 7 | 6 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0003 | 0/0 | 1563 | 57 | 3 | 12 | 30 | 2 | 10 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0004 | 0/1 | 1563 | 29 | 2 | 7 | 9 | 3 | 7 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0005 | 0/0 | 1563 | 14 | 12 | 1 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0006 | 0/0 | 1563 | 12 | 12 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0007 | 0/0 | 1563 | 10 | 10 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0008 | 0/0 | 1563 | 9 | 8 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0009 | 0/0 | 1563 | 7 | 6 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0010 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0011 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0012 | 0/0 | 1563 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0013 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0014 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0015 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0016 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0017 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0018 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0019 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0020 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0021 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0022 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
c0023 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0001 | 1/1 | 798 | 126 | 39 | 24 | 38 | 5 | 18 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0002 | 0/0 | 798 | 95 | 1 | 17 | 74 | 0 | 3 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0003 | 0/0 | 798 | 77 | 7 | 23 | 34 | 7 | 6 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0004 | 0/0 | 798 | 52 | 20 | 15 | 1 | 6 | 10 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0005 | 0/0 | 798 | 15 | 13 | 1 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0006 | 0/0 | 798 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0007 | 0/0 | 798 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0008 | 0/0 | 798 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0009 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0010 | 0/0 | 798 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0011 | 0/0 | 798 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0012 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
t0013 | 0/0 | 798 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0000 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0001 | 0/0 | 29 | 1 | 6 | 18 | 2 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0002 | 0/0 | 26 | 0 | 6 | 20 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0003 | 0/0 | 20 | 1 | 4 | 14 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0004 | 0/0 | 11 | 0 | 3 | 6 | 0 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0005 | 0/1 | 9 | 2 | 2 | 1 | 1 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0007 | 0/0 | 9 | 0 | 7 | 0 | 2 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0008 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0009 | 0/0 | 6 | 0 | 2 | 0 | 0 | 4 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0011 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0012 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0014 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0017 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0025 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0026 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0028 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0029 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0001 | 1/0 | 1563 | 146 | 22 | 30 | 73 | 6 | 14 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0002 | 0/0 | 1563 | 78 | 7 | 24 | 34 | 7 | 6 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0006 | 0/0 | 1563 | 12 | 12 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0012 | 0/0 | 1563 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0014 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0017 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0018 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0020 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0021 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0023 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0002c0003 | 0/0 | 1563 | 57 | 3 | 12 | 30 | 2 | 10 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0003c0004 | 0/1 | 1563 | 29 | 2 | 7 | 9 | 3 | 7 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004c0007 | 0/0 | 1563 | 10 | 10 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004c0008 | 0/0 | 1563 | 9 | 8 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004c0010 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0005c0005 | 0/0 | 1563 | 14 | 12 | 1 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0006c0009 | 0/0 | 1563 | 7 | 6 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0007c0011 | 0/0 | 1563 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0008c0022 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0009c0015 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0010c0016 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0011c0019 | 0/0 | 1563 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0012c0013 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0000t0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0001t0001 | 1/0 | 2360 | 5 | 3 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0001t0002 | 0/0 | 2360 | 88 | 1 | 14 | 71 | 0 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0001t0004 | 0/0 | 2360 | 50 | 18 | 15 | 1 | 6 | 10 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0001t0010 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0001t0012 | 0/0 | 2360 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0001t0013 | 0/0 | 2360 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0002t0002 | 0/0 | 2360 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0002t0003 | 0/0 | 2360 | 72 | 3 | 22 | 34 | 7 | 6 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0002t0006 | 0/0 | 2360 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0006t0001 | 0/0 | 2360 | 12 | 12 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0012t0001 | 0/0 | 2360 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0014t0003 | 0/0 | 2360 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0017t0002 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0018t0005 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0020t0002 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0021t0003 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0001c0023t0002 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0002c0003t0001 | 0/0 | 2360 | 56 | 3 | 12 | 29 | 2 | 10 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0002c0003t0009 | 0/0 | 2360 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0003c0004t0001 | 0/1 | 2360 | 29 | 2 | 7 | 9 | 3 | 7 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004c0007t0001 | 0/0 | 2360 | 8 | 8 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004c0007t0003 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004c0008t0001 | 0/0 | 2360 | 6 | 5 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004c0008t0007 | 0/0 | 2360 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0004c0010t0001 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0005c0005t0005 | 0/0 | 2360 | 14 | 12 | 1 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0006c0009t0001 | 0/0 | 2360 | 5 | 4 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0006c0009t0008 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0007c0011t0004 | 0/0 | 2360 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0008c0022t0002 | 0/0 | 2360 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0009c0015t0003 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0010c0016t0001 | 0/0 | 2360 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0011c0019t0002 | 0/0 | 2360 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
a0012c0013t0011 | 0/0 | 2360 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | copy fasta | chr19 | 15873023 | 15903074 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0000t0000g0000 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0001g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0002 | 0/0 | 26 | 0 | 6 | 20 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0008 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0011 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0016 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0014 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0024 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0025 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0028 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0010g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0012g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0001t0013g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0001 | 0/0 | 29 | 1 | 6 | 18 | 2 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0007 | 0/0 | 9 | 0 | 7 | 0 | 2 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0012 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0029 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0006g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0002t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0006t0001g0010 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0006t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0006t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0006t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0012t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0014t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0017t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0018t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0020t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0021t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0001c0023t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0003 | 0/0 | 20 | 1 | 4 | 14 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0004 | 0/0 | 11 | 0 | 3 | 6 | 0 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0018 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0026 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0002c0003t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0005 | 0/1 | 9 | 2 | 2 | 1 | 1 | 2 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0009 | 0/0 | 6 | 0 | 2 | 0 | 0 | 4 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0003c0004t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0007t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0008t0001g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0008t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0008t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0008t0007g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0008t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0010t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0004c0010t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0017 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0005c0005t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0006c0009t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0006c0009t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0006c0009t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0006c0009t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0006c0009t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0006c0009t0008g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0007c0011t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0008c0022t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0009c0015t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0010c0016t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0011c0019t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
a0012c0013t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0007 | EUR | GBR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0018 | EUR | GBR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00140 | hp1 | a0002 | c0003 | t0001 | g0128 | EUR | GBR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0001 | EUR | GBR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00280 | hp1 | a0001 | c0002 | t0003 | g0050 | EUR | FIN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0111 | EUR | FIN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00323 | hp1 | a0003 | c0004 | t0001 | g0005 | EUR | FIN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00323 | hp2 | a0001 | c0002 | t0003 | g0001 | EUR | FIN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00438 | hp1 | a0003 | c0004 | t0001 | g0013 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00544 | hp2 | a0003 | c0004 | t0001 | g0031 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00597 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0145 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00639 | hp1 | a0003 | c0004 | t0001 | g0009 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00639 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00735 | hp2 | a0001 | c0002 | t0003 | g0095 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0050 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00738 | hp2 | a0002 | c0003 | t0001 | g0124 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00741 | hp1 | a0003 | c0004 | t0001 | g0009 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01069 | hp2 | a0006 | c0009 | t0001 | g0099 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0154 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01070 | hp2 | a0001 | c0012 | t0001 | g0034 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01071 | hp2 | a0001 | c0012 | t0001 | g0034 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0155 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01074 | hp2 | a0003 | c0004 | t0001 | g0005 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01081 | hp2 | a0001 | c0002 | t0003 | g0049 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01109 | hp1 | a0004 | c0008 | t0001 | g0019 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01109 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01167 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01168 | hp1 | a0002 | c0003 | t0001 | g0003 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01168 | hp2 | a0003 | c0004 | t0001 | g0056 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01192 | hp2 | a0001 | c0002 | t0003 | g0029 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PUR | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0007 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01255 | hp2 | a0002 | c0003 | t0001 | g0160 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01257 | hp2 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0024 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01258 | hp2 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01261 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0076 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01346 | hp2 | a0005 | c0005 | t0005 | g0017 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01433 | hp2 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01515 | hp1 | a0003 | c0004 | t0001 | g0030 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0168 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0028 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0025 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0025 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01517 | hp2 | a0003 | c0004 | t0001 | g0030 | EUR | IBS | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01891 | hp1 | a0001 | c0006 | t0001 | g0033 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01891 | hp2 | a0012 | c0013 | t0011 | g0062 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01928 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01928 | hp2 | a0008 | c0022 | t0002 | g0119 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01934 | hp1 | a0003 | c0004 | t0001 | g0005 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01975 | hp2 | a0003 | c0004 | t0001 | g0057 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01978 | hp1 | a0003 | c0004 | t0001 | g0058 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0003 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01981 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0148 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0007 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02027 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02040 | hp2 | a0001 | c0002 | t0003 | g0151 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02055 | hp1 | a0005 | c0005 | t0005 | g0142 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02071 | hp2 | a0001 | c0020 | t0002 | g0069 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02074 | hp1 | a0001 | c0002 | t0003 | g0147 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02083 | hp1 | a0001 | c0002 | t0003 | g0163 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0122 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0102 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02145 | hp2 | a0001 | c0006 | t0001 | g0010 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02257 | hp2 | a0004 | c0010 | t0001 | g0174 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02258 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02258 | hp2 | a0005 | c0005 | t0005 | g0017 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0149 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02293 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02300 | hp1 | a0001 | c0002 | t0003 | g0012 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PEL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02451 | hp2 | a0001 | c0002 | t0006 | g0043 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02523 | hp1 | a0003 | c0004 | t0001 | g0031 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02523 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02572 | hp1 | a0001 | c0002 | t0006 | g0068 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02630 | hp1 | a0005 | c0005 | t0005 | g0123 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02647 | hp1 | a0009 | c0015 | t0003 | g0067 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02647 | hp2 | a0004 | c0008 | t0001 | g0032 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02698 | hp1 | a0003 | c0004 | t0001 | g0005 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02698 | hp2 | a0001 | c0001 | t0012 | g0161 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02717 | hp1 | a0004 | c0008 | t0007 | g0179 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02717 | hp2 | a0005 | c0005 | t0005 | g0017 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02735 | hp1 | a0001 | c0002 | t0003 | g0167 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0101 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02738 | hp2 | a0010 | c0016 | t0001 | g0132 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02809 | hp1 | a0005 | c0005 | t0005 | g0138 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02809 | hp2 | a0005 | c0005 | t0005 | g0027 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02818 | hp1 | a0004 | c0008 | t0001 | g0032 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02818 | hp2 | a0004 | c0007 | t0001 | g0171 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02886 | hp1 | a0001 | c0006 | t0001 | g0063 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02886 | hp2 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02895 | hp1 | a0006 | c0009 | t0001 | g0097 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02896 | hp1 | a0006 | c0009 | t0008 | g0046 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02896 | hp2 | a0005 | c0005 | t0005 | g0136 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02897 | hp1 | a0006 | c0009 | t0008 | g0046 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02922 | hp2 | a0004 | c0010 | t0001 | g0178 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02965 | hp1 | a0004 | c0007 | t0001 | g0170 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02970 | hp1 | a0005 | c0005 | t0005 | g0027 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02976 | hp1 | a0001 | c0006 | t0001 | g0010 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02976 | hp2 | a0001 | c0006 | t0001 | g0066 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03017 | hp1 | a0003 | c0004 | t0001 | g0059 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0094 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03041 | hp1 | a0001 | c0006 | t0001 | g0010 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03041 | hp2 | a0001 | c0021 | t0003 | g0143 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03098 | hp1 | a0004 | c0007 | t0003 | g0172 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03098 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03130 | hp1 | a0004 | c0007 | t0003 | g0169 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03130 | hp2 | a0004 | c0007 | t0001 | g0175 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03139 | hp2 | a0001 | c0006 | t0001 | g0064 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03209 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03209 | hp2 | a0004 | c0008 | t0001 | g0019 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03225 | hp1 | a0006 | c0009 | t0001 | g0098 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03225 | hp2 | a0006 | c0009 | t0001 | g0100 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03453 | hp1 | a0007 | c0011 | t0004 | g0035 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03453 | hp2 | a0004 | c0007 | t0001 | g0176 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03486 | hp1 | a0004 | c0008 | t0007 | g0054 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03486 | hp2 | a0007 | c0011 | t0004 | g0035 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03490 | hp1 | a0011 | c0019 | t0002 | g0109 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03490 | hp2 | a0003 | c0004 | t0001 | g0009 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0125 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03491 | hp2 | a0002 | c0003 | t0001 | g0026 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03492 | hp1 | a0003 | c0004 | t0001 | g0009 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03492 | hp2 | a0002 | c0003 | t0001 | g0026 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0105 | AFR | ESN | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03540 | hp1 | a0001 | c0002 | t0006 | g0115 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03579 | hp2 | a0001 | c0006 | t0001 | g0065 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03669 | hp2 | a0002 | c0003 | t0001 | g0004 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0153 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0159 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03704 | hp1 | a0002 | c0003 | t0001 | g0131 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0028 | SAS | PJL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03831 | hp1 | a0001 | c0001 | t0013 | g0085 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03831 | hp2 | a0001 | c0002 | t0003 | g0157 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03834 | hp1 | a0002 | c0003 | t0001 | g0004 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03834 | hp2 | a0002 | c0003 | t0001 | g0141 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03927 | hp1 | a0001 | c0002 | t0003 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03927 | hp2 | a0003 | c0004 | t0001 | g0005 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0134 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04115 | hp1 | a0002 | c0003 | t0001 | g0003 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04115 | hp2 | a0002 | c0003 | t0001 | g0140 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04184 | hp1 | a0003 | c0004 | t0001 | g0009 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0001 | SAS | BEB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04204 | hp2 | a0005 | c0005 | t0005 | g0017 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0091 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG04228 | hp2 | a0001 | c0002 | t0003 | g0152 | SAS | STU | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18522 | hp1 | a0004 | c0007 | t0001 | g0173 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18522 | hp2 | a0004 | c0007 | t0001 | g0053 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | CHB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | CHB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18906 | hp2 | a0001 | c0006 | t0001 | g0010 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18941 | hp1 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18944 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18949 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18951 | hp2 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18960 | hp1 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18960 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18963 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18963 | hp2 | a0001 | c0001 | t0010 | g0072 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18964 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18966 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18968 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18968 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18974 | hp2 | a0002 | c0003 | t0009 | g0130 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18975 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18979 | hp2 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18985 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18986 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18987 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18989 | hp1 | a0001 | c0017 | t0002 | g0086 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18989 | hp2 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18990 | hp1 | a0001 | c0023 | t0002 | g0120 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18990 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18991 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18991 | hp2 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18994 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18997 | hp1 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18997 | hp2 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19002 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19002 | hp2 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19003 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19005 | hp2 | a0003 | c0004 | t0001 | g0060 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19006 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19006 | hp2 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19007 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19009 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19043 | hp1 | a0001 | c0006 | t0001 | g0010 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19043 | hp2 | a0005 | c0005 | t0005 | g0027 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19054 | hp2 | a0000 | c0000 | t0000 | g0000 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19056 | hp1 | a0001 | c0002 | t0003 | g0158 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19058 | hp1 | a0002 | c0003 | t0001 | g0135 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19068 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19070 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19075 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19077 | hp2 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19080 | hp2 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19082 | hp2 | a0003 | c0004 | t0001 | g0013 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19083 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19085 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19085 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19086 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19088 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19090 | hp2 | a0002 | c0003 | t0001 | g0133 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19240 | hp1 | a0001 | c0006 | t0001 | g0033 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA19240 | hp2 | a0005 | c0005 | t0005 | g0144 | AFR | YRI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20129 | hp1 | a0001 | c0018 | t0005 | g0121 | AFR | ASW | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20129 | hp2 | a0001 | c0002 | t0006 | g0043 | AFR | ASW | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | TSI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0049 | EUR | TSI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0024 | EUR | TSI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0007 | EUR | TSI | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0092 | SAS | GIH | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20905 | hp2 | a0003 | c0004 | t0001 | g0009 | SAS | GIH | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG01123 | hp2 | a0001 | c0014 | t0003 | g0146 | AMR | CLM | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02109 | hp1 | a0004 | c0008 | t0001 | g0019 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02109 | hp2 | a0005 | c0005 | t0005 | g0139 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02486 | hp1 | a0005 | c0005 | t0005 | g0137 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02486 | hp2 | a0004 | c0008 | t0007 | g0054 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0104 | AFR | ACB | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0127 | AFR | USA | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
HG06807 | hp2 | a0004 | c0007 | t0001 | g0177 | AFR | USA | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0150 | EAS | JPT | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0010 | AFR | USA | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA20300 | hp2 | a0004 | c0008 | t0001 | g0061 | AFR | USA | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA21309 | hp1 | a0004 | c0007 | t0001 | g0053 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
NA21309 | hp2 | a0006 | c0009 | t0001 | g0116 | AFR | LWK | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
homoSapiens_chm13v2 | hp1 | a0003 | c0004 | t0001 | g0005 | REF | REF | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0112 | REF | REF | CYP4F2_chr19_15873023_15903074 | CYP4F2 | chr19 | 15873023 | 15903074 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15878779
|
G | T | 1 | a0005 | 14 | HG01346.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
missense_variant | MODERATE | c.1555C>A | p.Leu519Met | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 1605/2361 | 1555/1563 | 519/520 | chr19 | 15878779 | ||
chr19:15879621
|
C | T | 3 | a0002a0003a0010 | 87 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(84): Show |
missense_variant | MODERATE | c.1297G>A | p.Val433Met | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 11/13 | 1347/2361 | 1297/1563 | 433/520 | chr19 | 15879621 | ||
chr19:15879844
|
C | T | 1 | a0010 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1169G>A | p.Arg390Gln | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 10/13 | 1219/2361 | 1169/1563 | 390/520 | chr19 | 15879844 | ||
chr19:15886018
|
G | C | 1 | a0011 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1021C>G | p.Leu341Val | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/13 | 1071/2361 | 1021/1563 | 341/520 | chr19 | 15886018 | ||
chr19:15890405
|
C | A | 1 | a0006 | 7 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
missense_variant | MODERATE | c.554G>T | p.Gly185Val | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/13 | 604/2361 | 554/1563 | 185/520 | chr19 | 15890405 | ||
chr19:15897475
|
C | T | 1 | a0009 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.137G>A | p.Arg46His | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 187/2361 | 137/1563 | 46/520 | chr19 | 15897475 | ||
chr19:15897476
|
G | A | 1 | a0008 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.136C>T | p.Arg46Cys | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 186/2361 | 136/1563 | 46/520 | chr19 | 15897476 | ||
chr19:15897566
|
C | G | 1 | a0007 | 2 | HG03453.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.46G>C | p.Ala16Pro | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 96/2361 | 46/1563 | 16/520 | chr19 | 15897566 | ||
chr19:15897578
|
A | C | 2 | a0003a0004 | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
missense_variant | MODERATE | c.34T>G | p.Trp12Gly | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 84/2361 | 34/1563 | 12/520 | chr19 | 15897578 | ||
chr19:15897592
|
G | T | 1 | a0012 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.20C>A | p.Ser7Tyr | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 70/2361 | 20/1563 | 7/520 | chr19 | 15897592 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15878813
|
G | A | 1 | a0001c0017 | 1 | NA18989.hp1 | synonymous_variant | LOW | c.1521C>T | p.Arg507Arg | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 1571/2361 | 1521/1563 | 507/520 | chr19 | 15878813 | ||
chr19:15885947
|
G | A | 1 | a0001c0018 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1092C>T | p.Asp364Asp | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/13 | 1142/2361 | 1092/1563 | 364/520 | chr19 | 15885947 | ||
chr19:15886010
|
G | A | 3 | a0001c0002a0001c0014a0009c0015 | 80 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
synonymous_variant | LOW | c.1029C>T | p.His343His | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/13 | 1079/2361 | 1029/1563 | 343/520 | chr19 | 15886010 | ||
chr19:15889510
|
A | G | 1 | a0004c0010 | 2 | HG02257.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.831T>C | p.Thr277Thr | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/13 | 881/2361 | 831/1563 | 277/520 | chr19 | 15889510 | ||
chr19:15889516
|
G | A | 2 | a0001c0012a0001c0020 | 3 | HG01070.hp2 HG01071.hp2 HG02071.hp2 |
synonymous_variant | LOW | c.825C>T | p.Arg275Arg | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/13 | 875/2361 | 825/1563 | 275/520 | chr19 | 15889516 | ||
chr19:15889549
|
G | A | 1 | a0001c0021 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.792C>T | p.His264His | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/13 | 842/2361 | 792/1563 | 264/520 | chr19 | 15889549 | ||
chr19:15892578
|
G | C | 1 | a0004c0010 | 2 | HG02257.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.348C>G | p.Ala116Ala | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 4/13 | 398/2361 | 348/1563 | 116/520 | chr19 | 15892578 | ||
chr19:15895513
|
G | A | 2 | a0004c0007a0004c0010 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
synonymous_variant | LOW | c.336C>T | p.Asn112Asn | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/13 | 386/2361 | 336/1563 | 112/520 | chr19 | 15895513 | ||
chr19:15895570
|
T | G | 2 | a0004c0007a0004c0010 | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
synonymous_variant | LOW | c.279A>C | p.Gly93Gly | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/13 | 329/2361 | 279/1563 | 93/520 | chr19 | 15895570 | ||
chr19:15895603
|
G | A | 2 | a0003c0004a0004c0008 | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
synonymous_variant | LOW | c.246C>T | p.Ala82Ala | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/13 | 296/2361 | 246/1563 | 82/520 | chr19 | 15895603 | ||
chr19:15897447
|
T | C | 7 | a0001c0006a0001c0012a0003c0004others(4): Show | 65 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(62): Show |
synonymous_variant | LOW | c.165A>G | p.Pro55Pro | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 215/2361 | 165/1563 | 55/520 | chr19 | 15897447 | ||
chr19:15897513
|
A | G | 1 | a0001c0014 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.99T>C | p.His33His | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 149/2361 | 99/1563 | 33/520 | chr19 | 15897513 | ||
chr19:15897537
|
G | A | 1 | a0001c0023 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.75C>T | p.Val25Val | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/13 | 125/2361 | 75/1563 | 25/520 | chr19 | 15897537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15878230
|
C | G | 3 | a0001c0001t0004a0001c0001t0012a0007c0011t0004 | 53 | HG00280.hp2 HG00733.hp2 HG01099.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*541G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 541 | chr19 | 15878230 | |||||
chr19:15878310
|
C | T | 1 | a0001c0001t0010 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*461G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 461 | chr19 | 15878310 | |||||
chr19:15878357
|
C | T | 2 | a0001c0018t0005a0005c0005t0005 | 15 | HG01346.hp2 HG02055.hp1 HG02109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 414 | chr19 | 15878357 | |||||
chr19:15878374
|
G | A | 6 | a0001c0002t0003a0001c0002t0006a0001c0014t0003others(3): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*397C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 397 | chr19 | 15878374 | |||||
chr19:15878595
|
C | T | 16 | a0001c0001t0002a0001c0001t0010a0001c0001t0013others(13): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*176G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 176 | chr19 | 15878595 | |||||
chr19:15878644
|
A | G | 1 | a0001c0002t0006 | 4 | HG02451.hp2 HG02572.hp1 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*127T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 127 | chr19 | 15878644 | |||||
chr19:15878699
|
G | T | 1 | a0002c0003t0009 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*72C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 72 | chr19 | 15878699 | |||||
chr19:15878713
|
T | C | 3 | a0001c0001t0012a0006c0009t0008a0012c0013t0011 | 4 | HG01891.hp2 HG02698.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*58A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 58 | chr19 | 15878713 | |||||
chr19:15878744
|
T | C | 1 | a0001c0001t0013 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*27A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 13/13 | 27 | chr19 | 15878744 | |||||
chr19:15898051
|
G | A | 1 | a0004c0008t0007 | 3 | HG02486.hp2 HG02717.hp1 HG03486.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-27C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/13 | chr19 | 15898051 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15879061
|
T | A | 43 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0002t0003g0153others(40): Show | 100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1398-125A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 12/12 | chr19 | 15879061 | ||||||
chr19:15879238
|
A | G | 114 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0002g0002others(111): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1397+108T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 12/12 | chr19 | 15879238 | ||||||
chr19:15879454
|
T | C | 1 | a0001c0001t0004g0111 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1315-26A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 11/12 | chr19 | 15879454 | ||||||
chr19:15879455
|
T | C | 1 | a0001c0001t0004g0111 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1315-27A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 11/12 | chr19 | 15879455 | ||||||
chr19:15879700
|
G | T | 3 | a0001c0001t0004g0020a0001c0001t0004g0071a0001c0001t0004g0102 | 5 | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250-32C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 10/12 | chr19 | 15879700 | ||||||
chr19:15879747
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1249+17G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 10/12 | chr19 | 15879747 | ||||||
chr19:15880200
|
G | GA | 3 | a0003c0004t0001g0013a0003c0004t0001g0031a0003c0004t0001g0060 | 8 | HG00438.hp1 HG00544.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1116-304dupT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880200 | ||||||
chr19:15880327
|
G | GA | 4 | a0001c0002t0003g0012a0001c0002t0003g0052a0001c0002t0003g0149others(1): Show | 10 | HG00741.hp2 HG01515.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1116-431dupT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880327 | ||||||
chr19:15880623
|
C | T | 31 | a0001c0002t0003g0001a0001c0002t0003g0007a0001c0002t0003g0012others(28): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1116-726G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880623 | ||||||
chr19:15880623
|
CA | C | 29 | a0001c0001t0002g0044a0001c0001t0004g0079a0001c0006t0001g0010others(26): Show | 44 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.1116-727delT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880623 | ||||||
chr19:15880866
|
C | T | 30 | a0001c0002t0003g0001a0001c0002t0003g0007a0001c0002t0003g0012others(27): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1116-969G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880866 | ||||||
chr19:15880968
|
G | A | 1 | a0002c0003t0001g0128 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1116-1071C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15880968 | ||||||
chr19:15881002
|
T | TG | 2 | a0001c0001t0002g0040a0001c0001t0002g0108 | 3 | NA18986.hp2 NA18992.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1116-1106_1116-110 others(5): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881002 | ||||||
chr19:15881007
|
GTGCACAC others(1): Show |
G | 2 | a0001c0001t0002g0040a0001c0001t0002g0108 | 3 | NA18986.hp2 NA18992.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1116-1118_1116-111 others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881007 | ||||||
chr19:15881104
|
C | G | 39 | a0002c0003t0001g0003a0002c0003t0001g0004a0002c0003t0001g0018others(36): Show | 96 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.1116-1207G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881104 | ||||||
chr19:15881382
|
A | T | 1 | a0001c0018t0005g0121 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1116-1485T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881382 | ||||||
chr19:15881509
|
G | A | 6 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(3): Show | 12 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1116-1612C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881509 | ||||||
chr19:15881543
|
T | C | 5 | a0001c0001t0004g0028a0001c0001t0004g0159a0001c0001t0004g0164others(2): Show | 7 | HG01192.hp1 HG01255.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116-1646A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881543 | ||||||
chr19:15881565
|
G | GGATA | 59 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0036others(56): Show | 118 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.1116-1672_1116-166 others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | ||||||
chr19:15881565
|
G | GGATAGAT others(1): Show |
10 | a0001c0001t0002g0008a0001c0001t0002g0023a0001c0001t0002g0083others(7): Show | 20 | HG00408.hp1 HG00673.hp2 HG02040.hp1 others(17): Show |
intron_variant | MODIFIER | c.1116-1676_1116-166 others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | ||||||
chr19:15881565
|
G | GGATAGAT others(5): Show |
2 | a0001c0001t0002g0087a0001c0001t0002g0107 | 2 | NA19081.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1116-1680_1116-166 others(16): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | ||||||
chr19:15881565
|
GGATA | G | 3 | a0001c0001t0004g0103a0004c0007t0001g0173a0004c0010t0001g0174 | 3 | HG02257.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1116-1672_1116-166 others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | ||||||
chr19:15881565
|
GGATAGAT others(13): Show |
G | 74 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0002t0003g0001others(71): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1116-1688_1116-166 others(24): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881565 | ||||||
chr19:15881569
|
A | G | 1 | a0001c0001t0001g0045 | 2 | HG01361.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1116-1672T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881569 | ||||||
chr19:15881712
|
G | A | 1 | a0003c0004t0001g0060 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1116-1815C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881712 | ||||||
chr19:15881743
|
A | G | 74 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0002t0003g0001others(71): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1116-1846T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881743 | ||||||
chr19:15881801
|
TA | T | 6 | a0001c0001t0002g0084a0001c0002t0003g0155a0002c0003t0001g0135others(3): Show | 6 | HG01074.hp1 HG01168.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116-1905delT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881801 | ||||||
chr19:15881808
|
A | T | 1 | a0004c0010t0001g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1116-1911T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881808 | ||||||
chr19:15881970
|
C | T | 8 | a0002c0003t0001g0004a0002c0003t0001g0018a0002c0003t0001g0048others(5): Show | 22 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1116-2073G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881970 | ||||||
chr19:15881972
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1116-2075G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15881972 | ||||||
chr19:15882008
|
G | T | 1 | a0001c0001t0002g0039 | 2 | HG00597.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1116-2111C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882008 | ||||||
chr19:15882184
|
G | A | 2 | a0006c0009t0001g0098a0006c0009t0008g0046 | 3 | HG02896.hp1 HG02897.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1116-2287C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882184 | ||||||
chr19:15882214
|
C | T | 1 | a0001c0020t0002g0069 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1116-2317G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882214 | ||||||
chr19:15882231
|
C | T | 40 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(37): Show | 98 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1116-2334G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882231 | ||||||
chr19:15882251
|
G | GAA | 33 | a0001c0002t0003g0001a0001c0002t0003g0007a0001c0002t0003g0012others(30): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1116-2356_1116-235 others(6): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882251 | ||||||
chr19:15882273
|
A | G | 2 | a0001c0001t0002g0083a0001c0001t0002g0106 | 2 | HG00408.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1116-2376T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882273 | ||||||
chr19:15882312
|
C | T | 1 | a0002c0003t0001g0133 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1116-2415G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882312 | ||||||
chr19:15882375
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1116-2478G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882375 | ||||||
chr19:15882463
|
AATGTTCT others(111): Show |
A | 105 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0002t0003g0001others(102): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1116-2684_1116-256 others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882463 | ||||||
chr19:15882725
|
A | G | 1 | a0010c0016t0001g0132 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1116-2828T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882725 | ||||||
chr19:15882756
|
G | T | 1 | a0002c0003t0001g0048 | 2 | NA18991.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1116-2859C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882756 | ||||||
chr19:15882795
|
A | G | 1 | a0002c0003t0001g0131 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1116-2898T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15882795 | ||||||
chr19:15883016
|
C | T | 1 | a0001c0001t0004g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1115+2908G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883016 | ||||||
chr19:15883179
|
A | G | 1 | a0006c0009t0001g0099 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1115+2745T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883179 | ||||||
chr19:15883301
|
T | TAAAAATG others(312): Show |
1 | a0001c0012t0001g0034 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1115+2622_1115+262 others(323): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883301 | ||||||
chr19:15883301
|
T | TAAAAATG others(313): Show |
1 | a0001c0006t0001g0065 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1115+2622_1115+262 others(324): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883301 | ||||||
chr19:15883301
|
T | TAAAAATG others(325): Show |
1 | a0012c0013t0011g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1115+2622_1115+262 others(336): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883301 | ||||||
chr19:15883301
|
T | TAAAAATG others(325): Show |
1 | a0001c0006t0001g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1115+2622_1115+262 others(336): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883301 | ||||||
chr19:15883622
|
C | T | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+2302G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883622 | ||||||
chr19:15883668
|
A | T | 176 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0114others(173): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1115+2256T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883668 | ||||||
chr19:15883683
|
T | C | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+2241A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883683 | ||||||
chr19:15883733
|
AATCAACC others(9): Show |
A | 1 | a0003c0004t0001g0057 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1115+2175_1115+219 others(20): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883733 | ||||||
chr19:15883861
|
C | T | 4 | a0001c0006t0001g0065a0001c0006t0001g0066a0001c0012t0001g0034others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1115+2063G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883861 | ||||||
chr19:15883920
|
A | G | 107 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0002t0002g0148others(104): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1115+2004T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883920 | ||||||
chr19:15883931
|
C | G | 2 | a0001c0001t0004g0078a0001c0001t0004g0079 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1115+1993G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883931 | ||||||
chr19:15883936
|
A | G | 6 | a0001c0006t0001g0065a0001c0006t0001g0066a0001c0012t0001g0034others(3): Show | 7 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115+1988T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883936 | ||||||
chr19:15883988
|
G | A | 1 | a0001c0002t0003g0051 | 2 | NA18994.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1115+1936C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15883988 | ||||||
chr19:15884114
|
G | A | 79 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0002t0002g0148others(76): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.1115+1810C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884114 | ||||||
chr19:15884223
|
G | A | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+1701C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884223 | ||||||
chr19:15884338
|
G | A | 14 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(11): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1115+1586C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884338 | ||||||
chr19:15884426
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1115+1498C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884426 | ||||||
chr19:15884429
|
T | A | 2 | a0004c0010t0001g0174a0004c0010t0001g0178 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1115+1495A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884429 | ||||||
chr19:15884485
|
A | T | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0006t0001g0065others(5): Show | 10 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1115+1439T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884485 | ||||||
chr19:15884599
|
C | A | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1115+1325G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884599 | ||||||
chr19:15884678
|
A | C | 1 | a0006c0009t0001g0097 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1115+1246T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884678 | ||||||
chr19:15884711
|
G | C | 2 | a0001c0002t0003g0165a0001c0002t0003g0166 | 2 | NA18979.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1115+1213C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884711 | ||||||
chr19:15884741
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1115+1183G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884741 | ||||||
chr19:15884751
|
G | A | 1 | a0002c0003t0001g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1115+1173C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884751 | ||||||
chr19:15884755
|
A | G | 1 | a0001c0006t0001g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1115+1169T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884755 | ||||||
chr19:15884852
|
C | T | 1 | a0003c0004t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1115+1072G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884852 | ||||||
chr19:15884944
|
C | T | 4 | a0001c0001t0004g0020a0001c0001t0004g0071a0001c0001t0004g0075others(1): Show | 6 | HG02145.hp1 HG02559.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115+980G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884944 | ||||||
chr19:15884978
|
C | T | 14 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(11): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1115+946G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884978 | ||||||
chr19:15884992
|
G | GCCTTGCT others(1): Show |
11 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(8): Show | 30 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1115+931_1115+932i others(10): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884992 | ||||||
chr19:15884996
|
G | T | 11 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(8): Show | 30 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1115+928C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884996 | ||||||
chr19:15884997
|
C | CT | 11 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(8): Show | 30 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1115+926_1115+927i others(3): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15884997 | ||||||
chr19:15885039
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1115+885C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885039 | ||||||
chr19:15885053
|
C | G | 1 | a0001c0001t0002g0081 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1115+871G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885053 | ||||||
chr19:15885092
|
T | C | 4 | a0002c0003t0001g0018a0002c0003t0001g0124a0002c0003t0001g0127others(1): Show | 7 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115+832A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885092 | ||||||
chr19:15885118
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1115+806C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885118 | ||||||
chr19:15885164
|
C | A | 65 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(62): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1115+760G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885164 | ||||||
chr19:15885168
|
G | A | 1 | a0001c0001t0002g0087 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1115+756C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885168 | ||||||
chr19:15885198
|
C | G | 4 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(1): Show | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115+726G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885198 | ||||||
chr19:15885198
|
C | T | 11 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(8): Show | 30 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1115+726G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885198 | ||||||
chr19:15885211
|
T | A | 1 | a0001c0001t0002g0108 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1115+713A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885211 | ||||||
chr19:15885435
|
A | G | 93 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(90): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1115+489T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885435 | ||||||
chr19:15885482
|
A | G | 14 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(11): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.1115+442T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885482 | ||||||
chr19:15885539
|
A | T | 101 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0002t0002g0148others(98): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1115+385T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885539 | ||||||
chr19:15885672
|
T | TA | 10 | a0001c0006t0001g0065a0001c0006t0001g0066a0001c0012t0001g0034others(7): Show | 12 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1115+251_1115+252i others(3): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885672 | ||||||
chr19:15885672
|
T | TG | 97 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0002t0002g0148others(94): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1115+251_1115+252i others(3): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885672 | ||||||
chr19:15885687
|
C | T | 12 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0006t0001g0065others(9): Show | 14 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1115+237G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885687 | ||||||
chr19:15885775
|
G | T | 3 | a0001c0002t0003g0050a0001c0002t0003g0152a0001c0002t0003g0153 | 4 | HG00280.hp1 HG00738.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115+149C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885775 | ||||||
chr19:15885870
|
G | A | 2 | a0001c0001t0004g0103a0001c0001t0004g0104 | 2 | HG02559.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1115+54C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885870 | ||||||
chr19:15885914
|
C | T | 6 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(3): Show | 7 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115+10G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 9/12 | chr19 | 15885914 | ||||||
chr19:15886097
|
C | T | 11 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(8): Show | 30 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.986-44G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 8/12 | chr19 | 15886097 | ||||||
chr19:15886207
|
C | T | 1 | a0001c0002t0006g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.985+35G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 8/12 | chr19 | 15886207 | ||||||
chr19:15886326
|
A | AC | 63 | a0001c0001t0004g0077a0001c0001t0004g0093a0001c0002t0002g0148others(60): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.919-19dupG | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886326 | ||||||
chr19:15886332
|
C | A | 4 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-24G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886332 | ||||||
chr19:15886506
|
C | T | 1 | a0006c0009t0001g0099 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.919-198G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886506 | ||||||
chr19:15886587
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.919-279A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886587 | ||||||
chr19:15886612
|
A | C | 14 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(11): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.919-304T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886612 | ||||||
chr19:15886711
|
C | T | 1 | a0001c0006t0001g0066 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.919-403G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886711 | ||||||
chr19:15886726
|
G | C | 14 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(11): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.919-418C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886726 | ||||||
chr19:15886754
|
G | A | 65 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(62): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.919-446C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886754 | ||||||
chr19:15886891
|
T | C | 1 | a0004c0007t0003g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.919-583A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15886891 | ||||||
chr19:15887101
|
A | T | 1 | a0004c0010t0001g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.919-793T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887101 | ||||||
chr19:15887112
|
C | T | 65 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(62): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.919-804G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887112 | ||||||
chr19:15887131
|
T | A | 1 | a0002c0003t0001g0140 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.919-823A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887131 | ||||||
chr19:15887193
|
G | GAC | 14 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(11): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.919-887_919-886dup others(2): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887193 | ||||||
chr19:15887209
|
G | T | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.919-901C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887209 | ||||||
chr19:15887327
|
T | A | 6 | a0001c0006t0001g0065a0001c0006t0001g0066a0001c0012t0001g0034others(3): Show | 8 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.919-1019A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887327 | ||||||
chr19:15887333
|
T | G | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.919-1025A>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887333 | ||||||
chr19:15887372
|
G | A | 145 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0114others(142): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.919-1064C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887372 | ||||||
chr19:15887385
|
AAAACACA others(7): Show |
A | 2 | a0001c0001t0002g0022a0001c0001t0002g0041 | 5 | NA18965.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-1091_919-1078d others(16): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887385 | ||||||
chr19:15887388
|
A | T | 99 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(96): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.919-1080T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887388 | ||||||
chr19:15887492
|
ATAGACAT others(81): Show |
A | 4 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-1272_919-1185d others(90): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887492 | ||||||
chr19:15887519
|
GAC | G | 14 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(11): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.919-1213_919-1212d others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887519 | ||||||
chr19:15887573
|
C | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0041 | 5 | NA18965.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.919-1265G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887573 | ||||||
chr19:15887574
|
G | A | 2 | a0002c0003t0001g0125a0002c0003t0001g0141 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.919-1266C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887574 | ||||||
chr19:15887601
|
G | C | 1 | a0005c0005t0005g0142 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.919-1293C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887601 | ||||||
chr19:15887822
|
A | G | 1 | a0006c0009t0001g0099 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.919-1514T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887822 | ||||||
chr19:15887867
|
C | T | 2 | a0004c0010t0001g0174a0004c0010t0001g0178 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.918+1556G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887867 | ||||||
chr19:15887898
|
G | A | 1 | a0004c0010t0001g0178 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.918+1525C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887898 | ||||||
chr19:15887931
|
C | T | 65 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(62): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.918+1492G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15887931 | ||||||
chr19:15888001
|
C | T | 4 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(1): Show | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.918+1422G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888001 | ||||||
chr19:15888021
|
CAGATAT | C | 99 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(96): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.918+1396_918+1401d others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888021 | ||||||
chr19:15888194
|
A | T | 4 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.918+1229T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888194 | ||||||
chr19:15888285
|
C | T | 6 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(3): Show | 7 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+1138G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888285 | ||||||
chr19:15888369
|
T | C | 1 | a0006c0009t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.918+1054A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888369 | ||||||
chr19:15888447
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.918+976G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888447 | ||||||
chr19:15888614
|
G | T | 5 | a0006c0009t0001g0097a0006c0009t0001g0098a0006c0009t0001g0099others(2): Show | 6 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.918+809C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888614 | ||||||
chr19:15888647
|
AAC | A | 5 | a0001c0001t0002g0080a0001c0001t0004g0015a0001c0001t0004g0073others(2): Show | 8 | HG02055.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.918+774_918+775del others(2): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888647 | ||||||
chr19:15888668
|
A | G | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+755T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888668 | ||||||
chr19:15888778
|
T | C | 1 | a0009c0015t0003g0067 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.918+645A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888778 | ||||||
chr19:15888788
|
A | G | 6 | a0006c0009t0001g0097a0006c0009t0001g0098a0006c0009t0001g0099others(3): Show | 7 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.918+635T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888788 | ||||||
chr19:15888817
|
C | T | 14 | a0002c0003t0001g0105a0003c0004t0001g0005a0003c0004t0001g0009others(11): Show | 36 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.918+606G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15888817 | ||||||
chr19:15889075
|
T | C | 1 | a0001c0002t0003g0157 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.918+348A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15889075 | ||||||
chr19:15889091
|
A | G | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+332T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15889091 | ||||||
chr19:15889134
|
A | G | 1 | a0001c0002t0003g0095 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.918+289T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15889134 | ||||||
chr19:15889356
|
C | T | 93 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(90): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.918+67G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 7/12 | chr19 | 15889356 | ||||||
chr19:15889700
|
G | T | 1 | a0001c0001t0004g0076 | 1 | HG01346.hp1 | splice_region_variant&intron_variant | LOW | c.648-7C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889700 | ||||||
chr19:15889758
|
C | A | 1 | a0004c0007t0003g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.648-65G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889758 | ||||||
chr19:15889799
|
T | A | 65 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(62): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.648-106A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889799 | ||||||
chr19:15889906
|
G | A | 1 | a0001c0002t0003g0158 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.648-213C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889906 | ||||||
chr19:15889929
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0002g0041 | 5 | NA18965.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.648-236C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15889929 | ||||||
chr19:15890118
|
C | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0088 | 4 | HG00408.hp2 HG02056.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.647+194G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15890118 | ||||||
chr19:15890230
|
GT | G | 2 | a0004c0008t0007g0054a0004c0008t0007g0179 | 3 | HG02486.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.647+81delA | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 6/12 | chr19 | 15890230 | ||||||
chr19:15890465
|
G | T | 1 | a0001c0002t0003g0165 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.526-32C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890465 | ||||||
chr19:15890574
|
A | C | 1 | a0001c0002t0003g0050 | 2 | HG00280.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.526-141T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890574 | ||||||
chr19:15890782
|
C | T | 1 | a0001c0018t0005g0121 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.526-349G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890782 | ||||||
chr19:15890789
|
G | A | 4 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(1): Show | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.526-356C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890789 | ||||||
chr19:15890819
|
G | A | 6 | a0006c0009t0001g0097a0006c0009t0001g0098a0006c0009t0001g0099others(3): Show | 7 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.526-386C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890819 | ||||||
chr19:15890924
|
A | G | 2 | a0004c0010t0001g0174a0004c0010t0001g0178 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.526-491T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890924 | ||||||
chr19:15890930
|
G | A | 64 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(61): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.526-497C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890930 | ||||||
chr19:15890934
|
C | T | 1 | a0001c0002t0003g0147 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.526-501G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890934 | ||||||
chr19:15890980
|
A | G | 1 | a0001c0001t0004g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.526-547T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15890980 | ||||||
chr19:15891000
|
G | A | 4 | a0001c0006t0001g0065a0001c0006t0001g0066a0001c0012t0001g0034others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.526-567C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891000 | ||||||
chr19:15891010
|
T | C | 1 | a0004c0007t0003g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.526-577A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891010 | ||||||
chr19:15891038
|
T | A | 4 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.526-605A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891038 | ||||||
chr19:15891042
|
G | T | 65 | a0001c0002t0002g0148a0001c0002t0002g0154a0001c0002t0003g0001others(62): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.526-609C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891042 | ||||||
chr19:15891378
|
C | T | 4 | a0006c0009t0001g0097a0006c0009t0001g0098a0006c0009t0001g0100others(1): Show | 5 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+931G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891378 | ||||||
chr19:15891487
|
C | T | 32 | a0001c0018t0005g0121a0001c0021t0003g0143a0002c0003t0001g0003others(29): Show | 72 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.525+822G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891487 | ||||||
chr19:15891552
|
A | G | 4 | a0001c0006t0001g0065a0001c0006t0001g0066a0001c0012t0001g0034others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+757T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891552 | ||||||
chr19:15891583
|
T | C | 8 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(5): Show | 9 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.525+726A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891583 | ||||||
chr19:15891694
|
G | A | 2 | a0004c0010t0001g0174a0004c0010t0001g0178 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.525+615C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891694 | ||||||
chr19:15891711
|
G | A | 15 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(12): Show | 22 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.525+598C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891711 | ||||||
chr19:15891727
|
C | A | 4 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(1): Show | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.525+582G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891727 | ||||||
chr19:15891792
|
C | T | 4 | a0001c0006t0001g0065a0001c0006t0001g0066a0001c0012t0001g0034others(1): Show | 5 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.525+517G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891792 | ||||||
chr19:15891846
|
G | C | 3 | a0004c0008t0001g0019a0004c0008t0001g0032a0004c0008t0001g0061 | 6 | HG01109.hp1 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+463C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891846 | ||||||
chr19:15891951
|
C | G | 1 | a0012c0013t0011g0062 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.525+358G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15891951 | ||||||
chr19:15892163
|
C | T | 1 | a0001c0001t0004g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.525+146G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 5/12 | chr19 | 15892163 | ||||||
chr19:15892600
|
A | T | 1 | a0001c0001t0001g0045 | 2 | HG01361.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.344-18T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892600 | ||||||
chr19:15892833
|
C | T | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.344-251G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892833 | ||||||
chr19:15892841
|
T | C | 31 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(28): Show | 61 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.344-259A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892841 | ||||||
chr19:15892885
|
C | T | 32 | a0001c0018t0005g0121a0001c0021t0003g0143a0002c0003t0001g0003others(29): Show | 72 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.344-303G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892885 | ||||||
chr19:15892908
|
A | C | 2 | a0004c0010t0001g0174a0004c0010t0001g0178 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.344-326T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892908 | ||||||
chr19:15892942
|
T | C | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0006c0009t0001g0097others(5): Show | 9 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.344-360A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15892942 | ||||||
chr19:15893046
|
A | G | 2 | a0004c0010t0001g0174a0004c0010t0001g0178 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.344-464T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893046 | ||||||
chr19:15893053
|
A | G | 1 | a0002c0003t0009g0130 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.344-471T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893053 | ||||||
chr19:15893061
|
T | C | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.344-479A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893061 | ||||||
chr19:15893110
|
G | A | 1 | a0004c0008t0001g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.344-528C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893110 | ||||||
chr19:15893129
|
T | C | 15 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(12): Show | 22 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.344-547A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893129 | ||||||
chr19:15893270
|
G | A | 1 | a0001c0002t0003g0162 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.344-688C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893270 | ||||||
chr19:15893280
|
T | TCCCAGAC others(11): Show |
2 | a0001c0006t0001g0065a0001c0012t0001g0034 | 3 | HG01070.hp2 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.344-716_344-699dup others(18): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893280 | ||||||
chr19:15893323
|
T | C | 3 | a0001c0002t0003g0147a0001c0002t0003g0150a0001c0002t0003g0163 | 3 | HG02074.hp1 HG02083.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.344-741A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893323 | ||||||
chr19:15893561
|
A | T | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.344-979T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893561 | ||||||
chr19:15893586
|
C | G | 26 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(23): Show | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.344-1004G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893586 | ||||||
chr19:15893672
|
G | A | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.344-1090C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893672 | ||||||
chr19:15893728
|
G | A | 148 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0114others(145): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.344-1146C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893728 | ||||||
chr19:15893771
|
G | A | 1 | a0001c0001t0002g0089 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.344-1189C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893771 | ||||||
chr19:15893955
|
C | G | 8 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(5): Show | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.344-1373G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893955 | ||||||
chr19:15893990
|
C | A | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.344-1408G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15893990 | ||||||
chr19:15894042
|
G | A | 1 | a0001c0001t0002g0090 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.344-1460C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894042 | ||||||
chr19:15894170
|
C | T | 1 | a0001c0002t0003g0095 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.343+1336G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894170 | ||||||
chr19:15894179
|
A | C | 4 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+1327T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894179 | ||||||
chr19:15894180
|
C | T | 4 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(1): Show | 5 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.343+1326G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894180 | ||||||
chr19:15894193
|
C | T | 26 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(23): Show | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.343+1313G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894193 | ||||||
chr19:15894206
|
G | A | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+1300C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894206 | ||||||
chr19:15894209
|
T | C | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+1297A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894209 | ||||||
chr19:15894271
|
C | T | 5 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(2): Show | 6 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.343+1235G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894271 | ||||||
chr19:15894294
|
C | T | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+1212G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894294 | ||||||
chr19:15894344
|
TGGTCCTG others(7): Show |
T | 1 | a0002c0003t0001g0129 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.343+1148_343+1161d others(16): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894344 | ||||||
chr19:15894350
|
T | C | 8 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(5): Show | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.343+1156A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894350 | ||||||
chr19:15894375
|
C | T | 167 | a0001c0001t0001g0045a0001c0001t0001g0113a0001c0001t0001g0114others(164): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.343+1131G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894375 | ||||||
chr19:15894386
|
T | A | 1 | a0001c0002t0006g0115 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.343+1120A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894386 | ||||||
chr19:15894422
|
A | G | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+1084T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894422 | ||||||
chr19:15894427
|
C | T | 1 | a0004c0007t0003g0169 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.343+1079G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894427 | ||||||
chr19:15894432
|
C | G | 2 | a0004c0008t0007g0054a0004c0008t0007g0179 | 3 | HG02486.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.343+1074G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894432 | ||||||
chr19:15894466
|
G | C | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+1040C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894466 | ||||||
chr19:15894467
|
G | T | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+1039C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894467 | ||||||
chr19:15894486
|
C | T | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+1020G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894486 | ||||||
chr19:15894490
|
A | G | 19 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(16): Show | 27 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.343+1016T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894490 | ||||||
chr19:15894593
|
C | A | 1 | a0004c0008t0001g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.343+913G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894593 | ||||||
chr19:15894711
|
G | T | 8 | a0001c0001t0001g0113a0001c0001t0001g0114a0006c0009t0001g0097others(5): Show | 9 | HG01069.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.343+795C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894711 | ||||||
chr19:15894764
|
C | T | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+742G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894764 | ||||||
chr19:15894775
|
C | T | 1 | a0004c0010t0001g0174 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.343+731G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894775 | ||||||
chr19:15894805
|
A | T | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.343+701T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894805 | ||||||
chr19:15894835
|
G | A | 4 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+671C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894835 | ||||||
chr19:15894865
|
G | T | 2 | a0001c0006t0001g0065a0001c0012t0001g0034 | 3 | HG01070.hp2 HG01071.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.343+641C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894865 | ||||||
chr19:15894931
|
G | A | 1 | a0001c0006t0001g0064 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.343+575C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894931 | ||||||
chr19:15894972
|
C | T | 2 | a0003c0004t0001g0009a0003c0004t0001g0030 | 8 | HG00639.hp1 HG00741.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.343+534G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894972 | ||||||
chr19:15894984
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.343+522G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15894984 | ||||||
chr19:15895010
|
G | T | 4 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+496C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895010 | ||||||
chr19:15895049
|
C | T | 1 | a0001c0001t0004g0073 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.343+457G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895049 | ||||||
chr19:15895166
|
G | A | 1 | a0004c0008t0001g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.343+340C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895166 | ||||||
chr19:15895211
|
G | C | 8 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(5): Show | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.343+295C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895211 | ||||||
chr19:15895264
|
T | A | 42 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0006t0001g0010others(39): Show | 74 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.343+242A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895264 | ||||||
chr19:15895288
|
G | A | 1 | a0005c0005t0005g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.343+218C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895288 | ||||||
chr19:15895291
|
T | C | 26 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(23): Show | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.343+215A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895291 | ||||||
chr19:15895335
|
A | G | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.343+171T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895335 | ||||||
chr19:15895358
|
A | G | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.343+148T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895358 | ||||||
chr19:15895368
|
A | G | 26 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(23): Show | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.343+138T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895368 | ||||||
chr19:15895425
|
T | C | 2 | a0004c0010t0001g0174a0004c0010t0001g0178 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.343+81A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895425 | ||||||
chr19:15895430
|
G | A | 1 | a0001c0001t0004g0092 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.343+76C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895430 | ||||||
chr19:15895438
|
C | A | 1 | a0001c0001t0004g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.343+68G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895438 | ||||||
chr19:15895455
|
C | T | 2 | a0006c0009t0001g0097a0006c0009t0001g0100 | 2 | HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.343+51G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895455 | ||||||
chr19:15895459
|
A | G | 4 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03130.hp2 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.343+47T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895459 | ||||||
chr19:15895484
|
C | CA | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.343+21dupT | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 3/12 | chr19 | 15895484 | ||||||
chr19:15895735
|
T | C | 8 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(5): Show | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-85A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895735 | ||||||
chr19:15895801
|
T | C | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.199-151A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895801 | ||||||
chr19:15895838
|
T | A | 1 | a0001c0001t0004g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.199-188A>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895838 | ||||||
chr19:15895867
|
ATCTG | A | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.199-221_199-218del others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895867 | ||||||
chr19:15895907
|
C | CATCT | 23 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(20): Show | 47 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.199-258_199-257ins others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895907 | ||||||
chr19:15895908
|
G | A | 4 | a0001c0001t0004g0094a0004c0007t0001g0175a0004c0007t0001g0176others(1): Show | 4 | HG03017.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-258C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15895908 | ||||||
chr19:15896011
|
C | A | 5 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(2): Show | 6 | HG02818.hp2 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.199-361G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896011 | ||||||
chr19:15896044
|
A | C | 26 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(23): Show | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.199-394T>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896044 | ||||||
chr19:15896058
|
GTCTA | G | 2 | a0001c0002t0003g0151a0001c0002t0006g0043 | 3 | HG02040.hp2 HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.199-412_199-409del others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896058 | ||||||
chr19:15896065
|
T | TATCC | 8 | a0001c0001t0004g0164a0001c0002t0003g0150a0001c0002t0003g0167others(5): Show | 9 | HG01069.hp2 HG01981.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.199-416_199-415ins others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | ||||||
chr19:15896065
|
T | TATCCATC others(1): Show |
5 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(2): Show | 11 | HG01891.hp1 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-416_199-415ins others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | ||||||
chr19:15896065
|
T | TATCCATC others(5): Show |
3 | a0001c0006t0001g0065a0001c0006t0001g0066a0001c0012t0001g0034 | 4 | HG01070.hp2 HG01071.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-416_199-415ins others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | ||||||
chr19:15896065
|
TATCTATC others(1): Show |
T | 7 | a0004c0007t0001g0173a0004c0007t0001g0175a0004c0007t0001g0176others(4): Show | 7 | HG02257.hp2 HG02922.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-423_199-416del others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | ||||||
chr19:15896065
|
TATCTATC others(5): Show |
T | 6 | a0001c0002t0003g0147a0004c0007t0001g0053a0004c0007t0001g0170others(3): Show | 7 | HG02074.hp1 HG02818.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-427_199-416del others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896065 | ||||||
chr19:15896069
|
T | C | 48 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0004g0028others(45): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.199-419A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896069 | ||||||
chr19:15896069
|
T | TATCC | 37 | a0001c0001t0001g0045a0001c0001t0002g0096a0001c0018t0005g0121others(34): Show | 78 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.199-423_199-420dup others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896069 | ||||||
chr19:15896069
|
T | TATCCATC others(1): Show |
2 | a0004c0008t0007g0054a0004c0008t0007g0179 | 3 | HG02486.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.199-427_199-420dup others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896069 | ||||||
chr19:15896069
|
TATCC | T | 6 | a0001c0001t0004g0037a0001c0001t0004g0070a0001c0001t0004g0101others(3): Show | 10 | HG01109.hp1 HG01123.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-423_199-420del others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896069 | ||||||
chr19:15896182
|
C | T | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.199-532G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896182 | ||||||
chr19:15896233
|
G | GCTAT | 84 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0008others(81): Show | 195 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.199-587_199-584dup others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | ||||||
chr19:15896233
|
G | GCTATCTA others(1): Show |
9 | a0001c0001t0002g0036a0001c0001t0004g0070a0001c0001t0004g0071others(6): Show | 11 | HG01081.hp2 HG01993.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.199-591_199-584dup others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | ||||||
chr19:15896233
|
G | GCTATCTA others(5): Show |
1 | a0001c0020t0002g0069 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.199-595_199-584dup others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | ||||||
chr19:15896233
|
GCTAT | G | 15 | a0001c0002t0003g0029a0001c0002t0006g0068a0001c0014t0003g0146others(12): Show | 27 | HG00140.hp1 HG00438.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.199-587_199-584del others(4): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | ||||||
chr19:15896233
|
GCTATCTA others(1): Show |
G | 25 | a0001c0001t0002g0055a0001c0021t0003g0143a0002c0003t0001g0003others(22): Show | 67 | HG00099.hp2 HG00544.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.199-591_199-584del others(8): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | ||||||
chr19:15896233
|
GCTATCTA others(5): Show |
G | 2 | a0002c0003t0001g0145a0006c0009t0001g0116 | 2 | HG00621.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.199-595_199-584del others(12): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896233 | ||||||
chr19:15896335
|
G | A | 1 | a0004c0008t0007g0054 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.199-685C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896335 | ||||||
chr19:15896380
|
G | A | 1 | a0002c0003t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.199-730C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896380 | ||||||
chr19:15896407
|
G | T | 4 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(1): Show | 10 | HG01891.hp1 HG02145.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-757C>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896407 | ||||||
chr19:15896508
|
C | T | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.199-858G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896508 | ||||||
chr19:15896543
|
T | C | 1 | a0001c0002t0003g0168 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.198+871A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896543 | ||||||
chr19:15896647
|
G | A | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+767C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896647 | ||||||
chr19:15896652
|
T | G | 2 | a0004c0010t0001g0174a0004c0010t0001g0178 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.198+762A>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896652 | ||||||
chr19:15896723
|
C | T | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+691G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896723 | ||||||
chr19:15896743
|
T | C | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+671A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896743 | ||||||
chr19:15896830
|
G | A | 1 | a0004c0008t0001g0019 | 3 | HG01109.hp1 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+584C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896830 | ||||||
chr19:15896840
|
C | T | 1 | a0001c0002t0006g0068 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.198+574G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896840 | ||||||
chr19:15896877
|
G | A | 3 | a0004c0008t0001g0019a0004c0008t0001g0032a0004c0008t0001g0061 | 6 | HG01109.hp1 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+537C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896877 | ||||||
chr19:15896960
|
G | A | 8 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(5): Show | 15 | HG01070.hp2 HG01071.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+454C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896960 | ||||||
chr19:15896974
|
A | G | 26 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(23): Show | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.198+440T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896974 | ||||||
chr19:15896990
|
G | A | 1 | a0001c0001t0002g0047 | 2 | NA18943.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.198+424C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15896990 | ||||||
chr19:15897012
|
C | T | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+402G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897012 | ||||||
chr19:15897072
|
T | G | 2 | a0001c0001t0002g0117a0001c0001t0002g0118 | 2 | HG02040.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.198+342A>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897072 | ||||||
chr19:15897094
|
T | C | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+320A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897094 | ||||||
chr19:15897225
|
A | T | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+189T>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897225 | ||||||
chr19:15897289
|
T | C | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.198+125A>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897289 | ||||||
chr19:15897359
|
C | T | 1 | a0002c0003t0001g0122 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.198+55G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 2/12 | chr19 | 15897359 | ||||||
chr19:15897624
|
A | G | 15 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(12): Show | 38 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.-1-12T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897624 | ||||||
chr19:15897634
|
C | T | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1-22G>A | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897634 | ||||||
chr19:15897654
|
G | A | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1-42C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897654 | ||||||
chr19:15897659
|
C | G | 26 | a0003c0004t0001g0005a0003c0004t0001g0009a0003c0004t0001g0013others(23): Show | 50 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.-1-47G>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897659 | ||||||
chr19:15897668
|
G | C | 3 | a0004c0007t0001g0175a0004c0007t0001g0176a0004c0007t0001g0177 | 3 | HG03130.hp2 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-1-56C>G | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897668 | ||||||
chr19:15897688
|
A | G | 11 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(8): Show | 12 | HG02257.hp2 HG02818.hp2 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.-1-76T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897688 | ||||||
chr19:15897702
|
A | G | 34 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(31): Show | 65 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-1-90T>C | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897702 | ||||||
chr19:15897829
|
G | A | 1 | a0001c0018t0005g0121 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-2+197C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897829 | ||||||
chr19:15897831
|
A | AAGAG | 34 | a0001c0006t0001g0010a0001c0006t0001g0033a0001c0006t0001g0063others(31): Show | 65 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.-2+191_-2+194dupCT others(2): Show |
CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897831 | ||||||
chr19:15897833
|
G | A | 31 | a0001c0021t0003g0143a0002c0003t0001g0003a0002c0003t0001g0004others(28): Show | 71 | HG00099.hp2 HG00140.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-2+193C>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897833 | ||||||
chr19:15897879
|
CTG | C | 32 | a0001c0001t0004g0028a0001c0001t0004g0159a0001c0001t0004g0164others(29): Show | 81 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.-2+145_-2+146delCA | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897879 | ||||||
chr19:15897992
|
A | AC | 13 | a0001c0001t0002g0055a0004c0007t0001g0053a0004c0007t0001g0170others(10): Show | 15 | HG02257.hp2 HG02486.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+33dupG | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15897992 | ||||||
chr19:15898012
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C | A | 13 | a0004c0007t0001g0053a0004c0007t0001g0170a0004c0007t0001g0171others(10): Show | 15 | HG02257.hp2 HG02486.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2+14G>T | CYP4F2 | ENSG00000186115.13 | transcript | ENST00000221700.11 | protein_coding | 1/12 | chr19 | 15898012 |