geneid | 126410 |
---|---|
ensemblid | ENSG00000171954.13 |
hgncid | 26820 |
symbol | CYP4F22 |
name | cytochrome P450 family 4 subfamily F member 22 |
refseq_nuc | NM_173483.4 |
refseq_prot | NP_775754.2 |
ensembl_nuc | ENST00000269703.8 |
ensembl_prot | ENSP00000269703.1 |
mane_status | MANE Select |
chr | chr19 |
start | 15508525 |
end | 15552317 |
strand | + |
ver | v1.2 |
region | chr19:15508525-15552317 |
region5000 | chr19:15503525-15557317 |
regionname0 | CYP4F22_chr19_15508525_15552317 |
regionname5000 | CYP4F22_chr19_15503525_15557317 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 531 | 349 | 72 | 74 | 135 | 18 | 48 | 98 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0002 | 0/0 | 531 | 17 | 17 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0003 | 0/0 | 531 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0004 | 0/0 | 531 | 3 | 1 | 0 | 2 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0005 | 0/0 | 531 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0006 | 0/0 | 531 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0007 | 0/0 | 531 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0008 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0009 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0010 | 0/0 | 531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0011 | 0/0 | 531 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0012 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1596 | 316 | 55 | 70 | 127 | 18 | 44 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0002 | 0/0 | 1596 | 17 | 5 | 2 | 6 | 0 | 4 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0003 | 0/0 | 1596 | 17 | 17 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0004 | 0/0 | 1596 | 9 | 9 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0005 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0006 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0007 | 0/0 | 1596 | 3 | 1 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0008 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0009 | 0/0 | 1596 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0010 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0011 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0012 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0013 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0014 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0015 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0016 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0017 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0018 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0019 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
c0020 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1013 | 136 | 12 | 22 | 64 | 14 | 23 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0002 | 0/0 | 1013 | 125 | 30 | 20 | 56 | 2 | 17 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0003 | 1/0 | 1013 | 58 | 14 | 24 | 13 | 2 | 4 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0004 | 0/0 | 1013 | 39 | 30 | 7 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0005 | 0/0 | 1014 | 8 | 6 | 1 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0006 | 0/0 | 1014 | 6 | 0 | 2 | 3 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0007 | 0/0 | 1013 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0008 | 0/0 | 1014 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0009 | 0/0 | 1033 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0010 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0011 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0012 | 0/0 | 1033 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0013 | 0/0 | 1013 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0014 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
t0015 | 0/0 | 1013 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1596 | 316 | 55 | 70 | 127 | 18 | 44 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0002 | 0/0 | 1596 | 17 | 5 | 2 | 6 | 0 | 4 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0004 | 0/0 | 1596 | 9 | 9 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0005 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0011 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0012 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0013 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0020 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0002c0003 | 0/0 | 1596 | 17 | 17 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0003c0008 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0004c0007 | 0/0 | 1596 | 3 | 1 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0005c0006 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0006c0016 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0006c0017 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0007c0009 | 0/0 | 1596 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0008c0018 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0009c0015 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0010c0010 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0011c0014 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0012c0019 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2608 | 119 | 4 | 20 | 58 | 14 | 22 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0002 | 0/0 | 2608 | 109 | 20 | 18 | 54 | 2 | 15 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0003 | 1/0 | 2608 | 45 | 6 | 23 | 10 | 2 | 3 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0004 | 0/0 | 2608 | 27 | 18 | 7 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0005 | 0/0 | 2609 | 3 | 2 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0006 | 0/0 | 2609 | 6 | 0 | 2 | 3 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0007 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0008 | 0/0 | 2609 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0009 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0012 | 0/0 | 2628 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0013 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0014 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0001t0015 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0002t0001 | 0/0 | 2608 | 4 | 0 | 0 | 3 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0002t0002 | 0/0 | 2608 | 4 | 1 | 1 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0002t0003 | 0/0 | 2608 | 7 | 3 | 1 | 2 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0002t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0002t0010 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0004t0001 | 0/0 | 2608 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0004t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0004t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0004t0007 | 0/0 | 2608 | 3 | 3 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0005t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0005t0004 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0011t0001 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0012t0002 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0013t0001 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0001c0020t0003 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0002c0003t0001 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0002c0003t0002 | 0/0 | 2608 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0002c0003t0003 | 0/0 | 2608 | 5 | 5 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0002c0003t0004 | 0/0 | 2608 | 4 | 4 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0002c0003t0005 | 0/0 | 2609 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0003c0008t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0003c0008t0004 | 0/0 | 2608 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0004c0007t0001 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0004c0007t0002 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0004c0007t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0005c0006t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0005c0006t0005 | 0/0 | 2609 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0006c0016t0005 | 0/0 | 2609 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0006c0017t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0007c0009t0001 | 0/0 | 2608 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0008c0018t0002 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0009c0015t0004 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0010c0010t0002 | 0/0 | 2608 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0011c0014t0011 | 0/0 | 2608 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
a0012c0019t0001 | 0/0 | 2608 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | copy fasta | chr19 | 15503525 | 15557317 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0116 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0001g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0002g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0003g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0004g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0008g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0013g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0014g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0001t0015g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0002t0010g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0004t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0005t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0005t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0005t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0011t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0012t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0013t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0001c0020t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0002c0003t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0003c0008t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0003c0008t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0003c0008t0004g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0004c0007t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0004c0007t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0004c0007t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0005c0006t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0005c0006t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0005c0006t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0006c0016t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0006c0017t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0007c0009t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0007c0009t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0008c0018t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0009c0015t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0010c0010t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0011c0014t0011g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
a0012c0019t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0361 | EUR | GBR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0365 | EUR | GBR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0356 | EUR | GBR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0354 | EUR | GBR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | FIN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0340 | EUR | FIN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | CHS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0150 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0366 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01074 | hp1 | a0001 | c0011 | t0001 | g0313 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0343 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0242 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01109 | hp1 | a0006 | c0016 | t0005 | g0129 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0358 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0256 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0369 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0126 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | PUR | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0319 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0029 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0119 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01361 | hp1 | a0010 | c0010 | t0002 | g0202 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0297 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01496 | hp1 | a0001 | c0013 | t0001 | g0360 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0103 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0338 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0370 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0140 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01891 | hp1 | a0001 | c0002 | t0004 | g0332 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0346 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0125 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0168 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0152 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0333 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0351 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02027 | hp1 | a0001 | c0001 | t0015 | g0159 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02040 | hp2 | a0004 | c0007 | t0002 | g0222 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0347 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02074 | hp1 | a0001 | c0012 | t0002 | g0220 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02083 | hp1 | a0001 | c0002 | t0010 | g0196 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0141 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0247 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02257 | hp1 | a0001 | c0005 | t0002 | g0015 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02257 | hp2 | a0012 | c0019 | t0001 | g0046 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0154 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0136 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0323 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02280 | hp2 | a0003 | c0008 | t0004 | g0233 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02451 | hp1 | a0001 | c0004 | t0001 | g0106 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0322 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0349 | EAS | KHV | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02572 | hp1 | a0005 | c0006 | t0005 | g0302 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02572 | hp2 | a0004 | c0007 | t0004 | g0111 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02615 | hp1 | a0001 | c0004 | t0007 | g0060 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02615 | hp2 | a0002 | c0003 | t0003 | g0363 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02630 | hp1 | a0002 | c0003 | t0002 | g0006 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02647 | hp1 | a0002 | c0003 | t0002 | g0007 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0161 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0355 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02717 | hp2 | a0005 | c0006 | t0002 | g0327 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0377 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02723 | hp2 | a0002 | c0003 | t0004 | g0341 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0172 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0331 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02809 | hp2 | a0006 | c0017 | t0002 | g0368 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02818 | hp1 | a0001 | c0004 | t0002 | g0173 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02818 | hp2 | a0002 | c0003 | t0002 | g0362 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0373 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02895 | hp2 | a0001 | c0004 | t0007 | g0109 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02896 | hp1 | a0002 | c0003 | t0004 | g0329 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02897 | hp1 | a0002 | c0003 | t0004 | g0330 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0091 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02922 | hp1 | a0005 | c0006 | t0005 | g0009 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02922 | hp2 | a0001 | c0002 | t0003 | g0008 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02965 | hp1 | a0003 | c0008 | t0001 | g0025 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02965 | hp2 | a0002 | c0003 | t0005 | g0315 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02970 | hp2 | a0001 | c0004 | t0004 | g0107 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02976 | hp1 | a0002 | c0003 | t0003 | g0004 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02976 | hp2 | a0002 | c0003 | t0004 | g0112 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0334 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0311 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03130 | hp1 | a0002 | c0003 | t0005 | g0328 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0143 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0108 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0286 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0317 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03225 | hp2 | a0008 | c0018 | t0002 | g0379 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0380 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03486 | hp1 | a0002 | c0003 | t0002 | g0189 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03516 | hp1 | a0001 | c0005 | t0004 | g0017 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0371 | AFR | ESN | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0010 | AFR | GWD | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0062 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0339 | SAS | PJL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0359 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0292 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04115 | hp1 | a0001 | c0002 | t0003 | g0248 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0251 | SAS | BEB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0353 | SAS | STU | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18522 | hp1 | a0001 | c0005 | t0004 | g0018 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0375 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | CHB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18747 | hp2 | a0001 | c0002 | t0003 | g0240 | EAS | CHB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18906 | hp1 | a0009 | c0015 | t0004 | g0221 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0289 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18952 | hp2 | a0001 | c0001 | t0014 | g0274 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0270 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0276 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18980 | hp1 | a0011 | c0014 | t0011 | g0288 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18983 | hp2 | a0001 | c0020 | t0003 | g0097 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18991 | hp1 | a0004 | c0007 | t0001 | g0285 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19011 | hp1 | a0007 | c0009 | t0001 | g0198 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19043 | hp1 | a0002 | c0003 | t0003 | g0167 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19043 | hp2 | a0002 | c0003 | t0003 | g0004 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19062 | hp2 | a0007 | c0009 | t0001 | g0197 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | YRI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0374 | AFR | ASW | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | ASW | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | TSI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0246 | EUR | TSI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0357 | EUR | TSI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | TSI | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | GIH | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | GIH | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0372 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | CLM | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0376 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02109 | hp2 | a0003 | c0008 | t0004 | g0378 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02486 | hp1 | a0001 | c0004 | t0007 | g0105 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0303 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0011 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | ACB | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | USA | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0065 | AFR | USA | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20300 | hp1 | a0002 | c0003 | t0003 | g0324 | AFR | USA | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0027 | AFR | USA | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0123 | AFR | LWK | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0138 | REF | REF | CYP4F22_chr19_15503525_15557317 | CYP4F22 | chr19 | 15503525 | 15557317 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15537576
|
C | T | 1 | a0012 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.463C>T | p.His155Tyr | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 6/14 | 630/2609 | 463/1596 | 155/531 | chr19 | 15537576 | ||
chr19:15537645
|
A | T | 3 | a0002a0006a0008 | 20 | HG01109.hp1 HG02280.hp1 HG02615.hp2 others(17): Show |
missense_variant | MODERATE | c.532A>T | p.Ser178Cys | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 6/14 | 699/2609 | 532/1596 | 178/531 | chr19 | 15537645 | ||
chr19:15537909
|
C | G | 2 | a0003a0008 | 4 | HG02109.hp2 HG02280.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.587C>G | p.Ser196Cys | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/14 | 754/2609 | 587/1596 | 196/531 | chr19 | 15537909 | ||
chr19:15540512
|
A | G | 1 | a0009 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.734A>G | p.Tyr245Cys | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 901/2609 | 734/1596 | 245/531 | chr19 | 15540512 | ||
chr19:15540514
|
C | T | 1 | a0004 | 3 | HG02040.hp2 HG02572.hp2 NA18991.hp1 |
missense_variant | MODERATE | c.736C>T | p.Arg246Cys | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 903/2609 | 736/1596 | 246/531 | chr19 | 15540514 | ||
chr19:15540554
|
C | G | 1 | a0011 | 1 | NA18980.hp1 | missense_variant | MODERATE | c.776C>G | p.Ala259Gly | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 943/2609 | 776/1596 | 259/531 | chr19 | 15540554 | ||
chr19:15540563
|
G | A | 1 | a0010 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.785G>A | p.Arg262Gln | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 952/2609 | 785/1596 | 262/531 | chr19 | 15540563 | ||
chr19:15540628
|
C | T | 1 | a0007 | 2 | NA19011.hp1 NA19062.hp2 |
missense_variant | MODERATE | c.850C>T | p.Arg284Trp | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 1017/2609 | 850/1596 | 284/531 | chr19 | 15540628 | ||
chr19:15551388
|
A | C | 2 | a0005a0006 | 5 | HG01109.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
missense_variant | MODERATE | c.1513A>C | p.Lys505Gln | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 1680/2609 | 1513/1596 | 505/531 | chr19 | 15551388 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15525354
|
C | T | 1 | a0001c0020 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.18C>T | p.Asp6Asp | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/14 | 185/2609 | 18/1596 | 6/531 | chr19 | 15525354 | ||
chr19:15537560
|
T | C | 1 | a0001c0004 | 9 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
synonymous_variant | LOW | c.447T>C | p.Gly149Gly | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 6/14 | 614/2609 | 447/1596 | 149/531 | chr19 | 15537560 | ||
chr19:15537904
|
G | A | 1 | a0001c0002 | 17 | HG01243.hp1 HG01256.hp2 HG01891.hp1 others(14): Show |
synonymous_variant | LOW | c.582G>A | p.Ala194Ala | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/14 | 749/2609 | 582/1596 | 194/531 | chr19 | 15537904 | ||
chr19:15540471
|
C | T | 1 | a0006c0017 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.693C>T | p.Ser231Ser | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 860/2609 | 693/1596 | 231/531 | chr19 | 15540471 | ||
chr19:15540555
|
G | A | 1 | a0001c0005 | 3 | HG02257.hp1 HG03516.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.777G>A | p.Ala259Ala | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 944/2609 | 777/1596 | 259/531 | chr19 | 15540555 | ||
chr19:15540624
|
G | A | 1 | a0001c0011 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.846G>A | p.Arg282Arg | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/14 | 1013/2609 | 846/1596 | 282/531 | chr19 | 15540624 | ||
chr19:15548111
|
C | T | 1 | a0001c0013 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.1140C>T | p.Asp380Asp | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/14 | 1307/2609 | 1140/1596 | 380/531 | chr19 | 15548111 | ||
chr19:15551309
|
G | A | 1 | a0001c0012 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.1434G>A | p.Gln478Gln | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 1601/2609 | 1434/1596 | 478/531 | chr19 | 15551309 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15551519
|
A | C | 1 | a0001c0001t0015 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*48A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 48 | chr19 | 15551519 | |||||
chr19:15551561
|
C | A | 3 | a0001c0001t0007a0001c0001t0008a0001c0004t0007 | 5 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*90C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 90 | chr19 | 15551561 | |||||
chr19:15551566
|
C | G | 1 | a0001c0001t0014 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 95 | chr19 | 15551566 | |||||
chr19:15551615
|
G | A | 1 | a0001c0001t0009 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*144G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 144 | chr19 | 15551615 | |||||
chr19:15551654
|
T | G | 44 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(41): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*183T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 183 | chr19 | 15551654 | |||||
chr19:15551662
|
G | T | 1 | a0001c0001t0013 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 191 | chr19 | 15551662 | |||||
chr19:15551733
|
C | A | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(22): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*262C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 262 | chr19 | 15551733 | |||||
chr19:15551758
|
C | CTCAGGCC others(13): Show |
2 | a0001c0001t0009a0001c0001t0012 | 2 | HG02258.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*300_*301insTTCTGG others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 301 | INFO_REALIGN_3_PRIME | chr19 | 15551758 | ||||
chr19:15551893
|
A | AC | 6 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(3): Show | 15 | HG00735.hp2 HG01109.hp1 HG01257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*431dupC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 432 | INFO_REALIGN_3_PRIME | chr19 | 15551893 | ||||
chr19:15551893
|
A | C | 1 | a0001c0002t0010 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*422A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 422 | chr19 | 15551893 | |||||
chr19:15551921
|
C | A | 16 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(13): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 450 | chr19 | 15551921 | |||||
chr19:15552083
|
C | A | 1 | a0011c0014t0011 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*612C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 14/14 | 612 | chr19 | 15552083 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:15508598
|
G | GGTGAGGG others(7): Show |
8 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0373others(5): Show | 8 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+16_-109+29dup others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15508598 | |||||
chr19:15508726
|
AC | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(17): Show | 20 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+150delC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15508726 | |||||
chr19:15508800
|
A | T | 63 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0334others(60): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.-109+217A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508800 | ||||||
chr19:15508827
|
C | T | 1 | a0001c0001t0001g0310 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+244C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508827 | ||||||
chr19:15508840
|
T | C | 2 | a0001c0005t0004g0017a0001c0005t0004g0018 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+257T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508840 | ||||||
chr19:15508883
|
T | G | 9 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0020others(6): Show | 9 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+300T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508883 | ||||||
chr19:15508992
|
C | T | 6 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0309others(3): Show | 6 | NA18969.hp2 NA18980.hp2 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+409C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15508992 | ||||||
chr19:15509069
|
T | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0376others(26): Show | 29 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-109+486T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509069 | ||||||
chr19:15509398
|
G | T | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+815G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509398 | ||||||
chr19:15509505
|
G | T | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+922G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509505 | ||||||
chr19:15509623
|
G | T | 9 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0020others(6): Show | 9 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1040G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509623 | ||||||
chr19:15509709
|
C | T | 8 | a0001c0001t0002g0293a0001c0001t0002g0294a0001c0001t0002g0295others(5): Show | 8 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+1126C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509709 | ||||||
chr19:15509718
|
C | T | 2 | a0001c0001t0002g0290a0001c0001t0003g0291 | 2 | HG02735.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-109+1135C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509718 | ||||||
chr19:15509765
|
C | T | 20 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(17): Show | 20 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+1182C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509765 | ||||||
chr19:15509802
|
C | A | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1219C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509802 | ||||||
chr19:15509854
|
C | CTCCT | 52 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0052others(49): Show | 52 | HG00323.hp1 HG00408.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.-109+1321_-109+132 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | |||||
chr19:15509854
|
C | CTCCTTCC others(1): Show |
34 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(31): Show | 35 | HG00642.hp1 HG01109.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-109+1317_-109+132 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | |||||
chr19:15509854
|
C | CTCCTTCC others(5): Show |
9 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0002g0312others(6): Show | 9 | HG01074.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1313_-109+132 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | |||||
chr19:15509854
|
C | CTCCTTCC others(9): Show |
1 | a0001c0002t0002g0311 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-109+1309_-109+132 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | |||||
chr19:15509854
|
CTCCT | C | 31 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(28): Show | 31 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-109+1321_-109+132 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | |||||
chr19:15509854
|
CTCCTTCC others(1): Show |
C | 6 | a0001c0001t0001g0170a0001c0001t0002g0169a0001c0001t0002g0370others(3): Show | 6 | HG00738.hp1 HG01884.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+1317_-109+132 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | |||||
chr19:15509854
|
CTCCTTCC others(5): Show |
C | 2 | a0001c0001t0001g0183a0001c0001t0004g0371 | 2 | HG02683.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-109+1313_-109+132 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509854 | |||||
chr19:15509889
|
C | CTTTCT | 9 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(6): Show | 9 | HG02015.hp2 HG03209.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1308_-109+130 others(9): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509889 | |||||
chr19:15509889
|
C | CTTTCTTT others(2): Show |
25 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0001g0265others(22): Show | 26 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.-109+1308_-109+130 others(13): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509889 | |||||
chr19:15509889
|
C | CTTTCTTT others(6): Show |
13 | a0001c0001t0001g0245a0001c0001t0001g0253a0001c0001t0002g0244others(10): Show | 13 | HG00558.hp2 HG01081.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-109+1308_-109+130 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509889 | |||||
chr19:15509889
|
C | T | 1 | a0001c0002t0003g0289 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-109+1306C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509889 | ||||||
chr19:15509892
|
C | CCTTTCTT others(25): Show |
1 | a0001c0001t0004g0186 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-109+1312_-109+131 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509892 | |||||
chr19:15509892
|
C | CCTTTCTT others(29): Show |
1 | a0001c0001t0004g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-109+1312_-109+131 others(40): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509892 | |||||
chr19:15509892
|
C | T | 1 | a0001c0001t0003g0287 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-109+1309C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509892 | ||||||
chr19:15509893
|
C | CTTCCTTT others(10): Show |
2 | a0001c0001t0001g0175a0001c0001t0003g0174 | 2 | HG03834.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.-109+1316_-109+131 others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509893 | |||||
chr19:15509893
|
C | CTTTCTTT others(6): Show |
26 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0193others(23): Show | 26 | HG00323.hp2 HG00621.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.-109+1312_-109+131 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509893 | |||||
chr19:15509893
|
C | T | 35 | a0001c0001t0001g0259a0001c0001t0001g0261a0001c0001t0001g0265others(32): Show | 36 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.-109+1310C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509893 | ||||||
chr19:15509896
|
C | T | 43 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0212others(40): Show | 44 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.-109+1313C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509896 | ||||||
chr19:15509897
|
C | T | 9 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(6): Show | 9 | HG02015.hp2 HG03209.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1314C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509897 | ||||||
chr19:15509900
|
C | CCTTTCTT others(9): Show |
3 | a0001c0001t0001g0147a0001c0001t0003g0148a0001c0001t0003g0149 | 3 | HG02004.hp2 HG03654.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-109+1320_-109+132 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509900 | |||||
chr19:15509900
|
C | CCTTTCTT others(13): Show |
2 | a0001c0001t0002g0146a0001c0001t0006g0145 | 2 | HG04228.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-109+1320_-109+132 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509900 | |||||
chr19:15509900
|
C | CCTTTCTT others(17): Show |
1 | a0001c0001t0003g0144 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-109+1320_-109+132 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509900 | |||||
chr19:15509900
|
C | CTTCTTTC others(7): Show |
1 | a0001c0001t0002g0246 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-109+1317_-109+131 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509900 | ||||||
chr19:15509900
|
C | CTTT | 7 | a0001c0001t0001g0253a0001c0001t0002g0249a0001c0001t0002g0252others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+1317_-109+131 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509900 | ||||||
chr19:15509900
|
C | CTTTCTTT others(4): Show |
2 | a0001c0001t0003g0247a0001c0002t0003g0248 | 2 | HG02148.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-109+1317_-109+131 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509900 | ||||||
chr19:15509900
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0178a0001c0001t0001g0182others(54): Show | 58 | HG00544.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.-109+1317C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509900 | ||||||
chr19:15509902
|
T | TTTCTTTC others(5): Show |
3 | a0001c0001t0001g0151a0001c0001t0003g0152a0001c0001t0006g0150 | 3 | HG00735.hp2 HG01978.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-109+1320_-109+132 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509902 | |||||
chr19:15509903
|
TC | T | 28 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0201others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.-109+1322delC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509903 | |||||
chr19:15509904
|
C | CCTTCCTT others(25): Show |
2 | a0001c0001t0001g0035a0001c0001t0004g0034 | 2 | HG03017.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.-109+1324_-109+132 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CCTTCCTT others(25): Show |
1 | a0001c0001t0002g0039 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-109+1324_-109+132 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CCTTCCTT others(25): Show |
1 | a0001c0001t0005g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-109+1324_-109+132 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CCTTT | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1331_-109+133 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CCTTTCCT others(5): Show |
1 | a0001c0001t0001g0113 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-109+1326_-109+132 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CCTTTCTT others(9): Show |
3 | a0001c0001t0001g0122a0001c0001t0003g0001a0001c0001t0004g0123 | 4 | HG01978.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CCTTTCTT others(17): Show |
1 | a0001c0001t0001g0121 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-109+1330_-109+133 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CCTTTCTT others(21): Show |
3 | a0001c0001t0001g0118a0001c0001t0004g0119a0001c0001t0004g0120 | 3 | HG01256.hp1 HG01258.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(32): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CCTTTCTT others(25): Show |
3 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0002g0117 | 3 | HG00280.hp2 HG02273.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509904 | |||||
chr19:15509904
|
C | CTTT | 22 | a0001c0001t0001g0175a0001c0001t0001g0190a0001c0001t0001g0191others(19): Show | 23 | HG00544.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.-109+1321_-109+132 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509904 | ||||||
chr19:15509904
|
C | CTTTCTTT others(4): Show |
2 | a0001c0001t0003g0188a0001c0001t0005g0187 | 2 | HG01257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-109+1321_-109+132 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509904 | ||||||
chr19:15509904
|
C | CTTTCTTT others(8): Show |
1 | a0001c0001t0001g0372 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-109+1321_-109+132 others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509904 | ||||||
chr19:15509904
|
C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0147a0001c0001t0001g0151others(83): Show | 87 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.-109+1321C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509904 | ||||||
chr19:15509905
|
CT | C | 10 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(7): Show | 10 | HG02015.hp2 HG02976.hp2 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.-109+1325delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509905 | |||||
chr19:15509906
|
T | C | 1 | a0001c0001t0003g0287 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-109+1323T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509906 | ||||||
chr19:15509906
|
T | TTCCTTCC others(25): Show |
1 | a0001c0001t0002g0028 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-109+1324_-109+132 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | |||||
chr19:15509906
|
T | TTCCTTCC others(17): Show |
2 | a0001c0001t0002g0031a0001c0001t0002g0032 | 2 | HG02735.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-109+1324_-109+132 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | |||||
chr19:15509906
|
T | TTCCTTCC others(21): Show |
2 | a0001c0001t0001g0030a0001c0001t0006g0029 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-109+1324_-109+132 others(32): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | |||||
chr19:15509906
|
T | TTCCTTCC others(13): Show |
7 | a0001c0001t0001g0040a0001c0001t0002g0041a0001c0001t0002g0042others(4): Show | 7 | HG01070.hp1 HG01496.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+1324_-109+132 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | |||||
chr19:15509906
|
T | TTTCC | 15 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(12): Show | 15 | HG00544.hp2 HG00609.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-109+1326_-109+132 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | |||||
chr19:15509906
|
T | TTTCCTTC others(1): Show |
19 | a0001c0001t0001g0002a0001c0001t0001g0210a0001c0001t0001g0212others(16): Show | 20 | HG00609.hp1 HG00741.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.-109+1326_-109+132 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | |||||
chr19:15509906
|
T | TTTCTTTC others(5): Show |
7 | a0001c0001t0001g0178a0001c0001t0002g0124a0001c0001t0002g0176others(4): Show | 7 | HG01934.hp1 HG02056.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509906 | |||||
chr19:15509908
|
T | C | 42 | a0001c0001t0001g0033a0001c0001t0001g0047a0001c0001t0001g0051others(39): Show | 42 | HG00408.hp2 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.-109+1325T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509908 | ||||||
chr19:15509910
|
T | C | 30 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(27): Show | 30 | HG00544.hp2 HG00609.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.-109+1327T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509910 | ||||||
chr19:15509910
|
T | TTTCCTTC others(1): Show |
3 | a0001c0001t0001g0182a0001c0001t0002g0180a0001c0001t0003g0181 | 3 | HG01168.hp1 HG03579.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.-109+1330_-109+133 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509910 | |||||
chr19:15509914
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0114a0001c0001t0001g0183others(25): Show | 28 | HG00741.hp1 HG01074.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.-109+1331T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509914 | ||||||
chr19:15509914
|
T | TTTCC | 9 | a0001c0001t0002g0380a0001c0001t0004g0090a0001c0001t0004g0091others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1339_-109+134 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509914 | |||||
chr19:15509918
|
C | CTTCT | 3 | a0001c0001t0002g0127a0001c0001t0004g0128a0001c0002t0002g0126 | 3 | HG01243.hp1 HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-109+1338_-109+133 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509918 | |||||
chr19:15509918
|
C | T | 182 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(179): Show | 185 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.-109+1335C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509918 | ||||||
chr19:15509922
|
C | CTCTTCTT others(11): Show |
1 | a0001c0001t0002g0166 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-109+1340_-109+134 others(22): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCCTTC others(5): Show |
5 | a0001c0001t0002g0013a0001c0001t0004g0010a0001c0001t0004g0012others(2): Show | 5 | HG02622.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+1342_-109+134 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCTTTC others(1): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0055others(3): Show | 6 | HG01975.hp2 HG03471.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+1358_-109+136 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCTTTC others(5): Show |
20 | a0001c0001t0001g0047a0001c0001t0001g0051a0001c0001t0001g0052others(17): Show | 20 | HG00408.hp2 HG00673.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+1354_-109+136 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCTTTC others(9): Show |
6 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG02055.hp2 HG02602.hp2 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+1350_-109+136 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCTTTC others(13): Show |
3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0002g0073 | 3 | HG01515.hp1 HG01517.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-109+1346_-109+136 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCTTTC others(17): Show |
5 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0068others(2): Show | 5 | HG00642.hp2 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-109+1342_-109+136 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCTTTC others(21): Show |
1 | a0001c0001t0003g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-109+1365_-109+136 others(32): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCTTTC others(25): Show |
3 | a0001c0001t0002g0064a0001c0001t0002g0290a0001c0001t0002g0370 | 3 | HG01884.hp1 HG02735.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-109+1365_-109+136 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | CTTCTTTC others(33): Show |
2 | a0001c0001t0001g0114a0006c0016t0005g0129 | 2 | HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-109+1365_-109+136 others(44): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509922 | |||||
chr19:15509922
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0035others(177): Show | 183 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-109+1339C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509922 | ||||||
chr19:15509926
|
T | C | 14 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0020others(11): Show | 14 | HG00621.hp2 HG01891.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.-109+1343T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509926 | ||||||
chr19:15509930
|
T | C | 2 | a0002c0003t0002g0006a0002c0003t0002g0007 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-109+1347T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509930 | ||||||
chr19:15509946
|
T | TTTCTTTC others(12): Show |
1 | a0001c0001t0002g0063 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-109+1365_-109+136 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509946 | |||||
chr19:15509947
|
T | TTCTTTCT others(27): Show |
1 | a0001c0001t0002g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-109+1365_-109+136 others(38): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509947 | |||||
chr19:15509954
|
G | GTC | 141 | a0001c0001t0001g0002a0001c0001t0001g0175a0001c0001t0001g0178others(138): Show | 143 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-109+1381_-109+138 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509954 | |||||
chr19:15509962
|
C | CTCTT | 3 | a0001c0001t0002g0312a0001c0002t0003g0331a0001c0002t0004g0332 | 3 | HG01891.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-109+1397_-109+140 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15509962 | |||||
chr19:15509962
|
C | T | 9 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0020others(6): Show | 9 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+1379C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509962 | ||||||
chr19:15509988
|
G | T | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1405G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15509988 | ||||||
chr19:15510187
|
G | T | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1604G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510187 | ||||||
chr19:15510197
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-109+1614G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510197 | ||||||
chr19:15510228
|
C | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(15): Show | 18 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.-109+1645C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510228 | ||||||
chr19:15510285
|
C | T | 2 | a0002c0003t0002g0006a0002c0003t0002g0007 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-109+1702C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510285 | ||||||
chr19:15510318
|
C | T | 1 | a0001c0001t0002g0117 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-109+1735C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510318 | ||||||
chr19:15510369
|
G | A | 326 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(323): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-109+1786G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510369 | ||||||
chr19:15510506
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-109+1923C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510506 | ||||||
chr19:15510507
|
G | A | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+1924G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510507 | ||||||
chr19:15510522
|
A | G | 81 | a0001c0001t0001g0005a0001c0001t0001g0320a0001c0001t0001g0321others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(79): Show |
intron_variant | MODIFIER | c.-109+1939A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510522 | ||||||
chr19:15510572
|
T | C | 1 | a0002c0003t0002g0362 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-109+1989T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510572 | ||||||
chr19:15510575
|
G | T | 8 | a0001c0001t0001g0223a0001c0001t0002g0224a0001c0001t0002g0225others(5): Show | 8 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+1992G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510575 | ||||||
chr19:15510598
|
A | G | 1 | a0001c0002t0002g0311 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-109+2015A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510598 | ||||||
chr19:15510606
|
A | T | 1 | a0001c0001t0004g0010 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-109+2023A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510606 | ||||||
chr19:15510637
|
C | G | 2 | a0001c0002t0003g0008a0005c0006t0005g0009 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-109+2054C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510637 | ||||||
chr19:15510692
|
T | C | 88 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(85): Show | 89 | HG00280.hp2 HG00408.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.-109+2109T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510692 | ||||||
chr19:15510797
|
AATTTAG | A | 7 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(4): Show | 7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+2216_-109+222 others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510797 | |||||
chr19:15510935
|
A | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(18): Show | 21 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+2352A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510935 | ||||||
chr19:15510945
|
C | CAT | 26 | a0001c0001t0001g0147a0001c0001t0001g0226a0001c0001t0001g0227others(23): Show | 26 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-109+2383_-109+238 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | |||||
chr19:15510945
|
C | CATAT | 10 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0130others(7): Show | 10 | HG00673.hp1 HG00738.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-109+2381_-109+238 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | |||||
chr19:15510945
|
C | CATATAT | 3 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0006g0029 | 3 | HG01257.hp2 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-109+2379_-109+238 others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | |||||
chr19:15510945
|
C | CATATATA others(3): Show |
1 | a0001c0001t0005g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-109+2375_-109+238 others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | |||||
chr19:15510945
|
CAT | C | 12 | a0001c0001t0001g0344a0001c0001t0001g0361a0001c0001t0002g0342others(9): Show | 12 | HG00099.hp1 HG01081.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.-109+2383_-109+238 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510945 | |||||
chr19:15510958
|
A | T | 6 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0004g0010others(3): Show | 6 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+2375A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510958 | ||||||
chr19:15510964
|
A | AT | 4 | a0001c0001t0001g0277a0001c0001t0002g0263a0001c0001t0006g0276others(1): Show | 4 | HG01167.hp2 NA18906.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+2382dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510964 | |||||
chr19:15510964
|
A | ATT | 9 | a0001c0001t0001g0209a0001c0001t0001g0223a0001c0001t0002g0225others(6): Show | 9 | HG00609.hp2 HG02040.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+2382_-109+238 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510964 | |||||
chr19:15510964
|
A | T | 7 | a0001c0004t0001g0106a0001c0004t0001g0108a0001c0004t0001g0110others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+2381A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510964 | ||||||
chr19:15510966
|
A | AT | 9 | a0001c0001t0001g0088a0001c0001t0001g0165a0001c0001t0001g0193others(6): Show | 9 | HG01361.hp1 HG02040.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-109+2400dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATAT | 7 | a0001c0001t0001g0265a0001c0001t0001g0279a0001c0001t0002g0177others(4): Show | 7 | HG00280.hp1 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0005 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0004g0012a0001c0001t0004g0016 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(36): Show |
1 | a0001c0001t0002g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(47): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(32): Show |
1 | a0001c0001t0002g0022 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(43): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(25): Show |
1 | a0001c0002t0003g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(36): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(28): Show |
1 | a0001c0001t0003g0023 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(39): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(26): Show |
1 | a0001c0001t0002g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(37): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0002g0013a0001c0001t0004g0010 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0004g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(8): Show |
1 | a0001c0002t0003g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0009g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATAT others(10): Show |
1 | a0003c0008t0001g0025 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATTT others(4): Show |
1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATATTT others(6): Show |
1 | a0001c0005t0002g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATT | 11 | a0001c0001t0001g0191a0001c0001t0001g0268a0001c0001t0001g0269others(8): Show | 11 | HG02080.hp2 HG04184.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATTTTT others(4): Show |
2 | a0002c0003t0002g0006a0002c0003t0002g0007 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATATTTTT others(7): Show |
1 | a0008c0018t0002g0379 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-109+2384_-109+238 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATT | 59 | a0001c0001t0001g0002a0001c0001t0001g0175a0001c0001t0001g0178others(56): Show | 60 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-109+2399_-109+240 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | ATTT | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0002g0003others(3): Show | 7 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-109+2398_-109+240 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
A | T | 30 | a0001c0001t0001g0078a0001c0001t0001g0209a0001c0001t0001g0223others(27): Show | 30 | HG00609.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.-109+2383A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510966 | ||||||
chr19:15510966
|
AT | A | 19 | a0001c0001t0001g0026a0001c0001t0001g0071a0001c0001t0001g0170others(16): Show | 20 | HG01515.hp1 HG02004.hp1 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.-109+2400delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510966
|
ATT | A | 31 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0335others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(28): Show |
intron_variant | MODIFIER | c.-109+2399_-109+240 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15510966 | |||||
chr19:15510967
|
T | TA | 7 | a0001c0001t0001g0135a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG00642.hp2 HG01243.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510967 | ||||||
chr19:15510967
|
T | TATATATA others(26): Show |
2 | a0001c0001t0002g0019a0001c0001t0002g0020 | 2 | HG01891.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-109+2384_-109+238 others(37): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510967 | ||||||
chr19:15510968
|
T | A | 93 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0040others(90): Show | 94 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.-109+2385T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510968 | ||||||
chr19:15510969
|
T | A | 5 | a0001c0001t0001g0071a0001c0001t0002g0063a0001c0001t0002g0290others(2): Show | 5 | HG01515.hp1 HG02071.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+2386T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510969 | ||||||
chr19:15510970
|
T | A | 24 | a0001c0001t0001g0047a0001c0001t0001g0122a0001c0001t0001g0156others(21): Show | 24 | HG01070.hp1 HG01255.hp1 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.-109+2387T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510970 | ||||||
chr19:15510972
|
T | A | 1 | a0001c0001t0001g0047 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-109+2389T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15510972 | ||||||
chr19:15511028
|
G | A | 1 | a0002c0003t0004g0112 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-109+2445G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511028 | ||||||
chr19:15511059
|
C | T | 1 | a0001c0005t0002g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-109+2476C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511059 | ||||||
chr19:15511062
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0170 | 3 | HG02004.hp1 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.-109+2479G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511062 | ||||||
chr19:15511075
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-109+2492T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511075 | ||||||
chr19:15511183
|
C | A | 8 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0020others(5): Show | 8 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-109+2600C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511183 | ||||||
chr19:15511208
|
C | A | 149 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.-109+2625C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511208 | ||||||
chr19:15511324
|
T | C | 3 | a0001c0001t0001g0376a0001c0001t0004g0375a0002c0003t0001g0377 | 3 | HG02109.hp1 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-109+2741T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511324 | ||||||
chr19:15511331
|
C | T | 1 | a0001c0001t0002g0278 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-109+2748C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511331 | ||||||
chr19:15511378
|
A | G | 1 | a0001c0001t0004g0242 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-109+2795A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511378 | ||||||
chr19:15511542
|
T | G | 1 | a0001c0001t0003g0349 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-109+2959T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511542 | ||||||
chr19:15511693
|
G | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0055others(6): Show | 9 | HG01257.hp2 HG01258.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.-109+3110G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511693 | ||||||
chr19:15511717
|
C | T | 2 | a0001c0005t0004g0017a0001c0005t0004g0018 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-109+3134C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511717 | ||||||
chr19:15511847
|
C | T | 3 | a0001c0001t0004g0090a0001c0001t0004g0091a0001c0001t0015g0159 | 3 | HG02027.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-109+3264C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511847 | ||||||
chr19:15511908
|
G | A | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-109+3325G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511908 | ||||||
chr19:15511954
|
G | A | 1 | a0001c0001t0004g0373 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-109+3371G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15511954 | ||||||
chr19:15512071
|
TATCAAAT others(12): Show |
T | 1 | a0001c0001t0001g0310 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+3490_-109+350 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15512071 | |||||
chr19:15512298
|
C | T | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+3715C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512298 | ||||||
chr19:15512314
|
T | C | 322 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(319): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-109+3731T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512314 | ||||||
chr19:15512324
|
A | G | 1 | a0001c0001t0001g0195 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-109+3741A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512324 | ||||||
chr19:15512395
|
G | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0175a0001c0001t0001g0178others(132): Show | 137 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-109+3812G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512395 | ||||||
chr19:15512719
|
G | T | 1 | a0001c0001t0002g0290 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-109+4136G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512719 | ||||||
chr19:15512819
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-109+4236A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512819 | ||||||
chr19:15512829
|
T | C | 6 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+4246T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15512829 | ||||||
chr19:15512992
|
T | TTC | 145 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(142): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-109+4429_-109+443 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15512992 | |||||
chr19:15512992
|
TTCTCTCT others(1): Show |
T | 21 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(18): Show | 21 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+4423_-109+443 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15512992 | |||||
chr19:15513091
|
G | A | 322 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(319): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-109+4508G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513091 | ||||||
chr19:15513129
|
G | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0207a0001c0001t0001g0235 | 3 | NA18967.hp1 NA19005.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-109+4546G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513129 | ||||||
chr19:15513240
|
T | A | 177 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0030others(174): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.-109+4657T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513240 | ||||||
chr19:15513274
|
C | G | 4 | a0001c0001t0002g0155a0001c0001t0004g0128a0001c0001t0004g0168others(1): Show | 4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+4691C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513274 | ||||||
chr19:15513333
|
G | T | 2 | a0001c0002t0003g0008a0005c0006t0005g0009 | 2 | HG02922.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-109+4750G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513333 | ||||||
chr19:15513349
|
G | GTA | 74 | a0001c0001t0001g0030a0001c0001t0001g0035a0001c0001t0001g0040others(71): Show | 75 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.-109+4778_-109+477 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15513349 | |||||
chr19:15513349
|
G | GTATA | 18 | a0001c0001t0001g0081a0001c0001t0001g0115a0001c0001t0001g0116others(15): Show | 19 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-109+4776_-109+477 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15513349 | |||||
chr19:15513361
|
AT | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0155others(14): Show | 17 | HG00733.hp2 HG01169.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.-109+4799delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15513361 | |||||
chr19:15513362
|
T | TA | 67 | a0001c0001t0001g0026a0001c0001t0001g0182a0001c0001t0001g0259others(64): Show | 67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-109+4779_-109+478 others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513362 | ||||||
chr19:15513362
|
T | TATA | 13 | a0001c0001t0001g0033a0001c0001t0001g0047a0001c0001t0001g0074others(10): Show | 13 | HG01891.hp2 HG02132.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-109+4779_-109+478 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513362 | ||||||
chr19:15513363
|
T | A | 239 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0035others(236): Show | 243 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-109+4780T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513363 | ||||||
chr19:15513364
|
T | A | 81 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0074others(78): Show | 81 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.-109+4781T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513364 | ||||||
chr19:15513365
|
T | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0035others(180): Show | 187 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.-109+4782T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513365 | ||||||
chr19:15513366
|
T | A | 35 | a0001c0001t0001g0047a0001c0001t0001g0245a0001c0001t0001g0259others(32): Show | 35 | HG00544.hp1 HG00558.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.-109+4783T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513366 | ||||||
chr19:15513367
|
T | A | 32 | a0001c0001t0001g0151a0001c0001t0001g0175a0001c0001t0001g0178others(29): Show | 32 | HG00323.hp2 HG00738.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-109+4784T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513367 | ||||||
chr19:15513368
|
T | A | 8 | a0001c0001t0001g0259a0001c0001t0001g0376a0001c0001t0002g0155others(5): Show | 8 | HG00544.hp1 HG02109.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-109+4785T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513368 | ||||||
chr19:15513369
|
T | A | 7 | a0001c0001t0001g0190a0001c0001t0001g0199a0001c0001t0001g0200others(4): Show | 7 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.-109+4786T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513369 | ||||||
chr19:15513371
|
T | A | 1 | a0001c0001t0009g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+4788T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513371 | ||||||
chr19:15513384
|
A | T | 1 | a0001c0001t0001g0310 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+4801A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513384 | ||||||
chr19:15513406
|
C | T | 1 | a0006c0017t0002g0368 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-109+4823C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513406 | ||||||
chr19:15513407
|
G | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(18): Show | 21 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+4824G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513407 | ||||||
chr19:15513409
|
G | T | 1 | a0001c0001t0001g0310 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+4826G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513409 | ||||||
chr19:15513457
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-109+4874C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513457 | ||||||
chr19:15513490
|
G | A | 9 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(6): Show | 9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-109+4907G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513490 | ||||||
chr19:15513538
|
T | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(18): Show | 21 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-109+4955T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513538 | ||||||
chr19:15513540
|
A | T | 1 | a0001c0001t0001g0310 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-109+4957A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513540 | ||||||
chr19:15513565
|
C | G | 139 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0147others(136): Show | 141 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.-109+4982C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513565 | ||||||
chr19:15513616
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-109+5033G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513616 | ||||||
chr19:15513743
|
C | T | 4 | a0001c0001t0002g0153a0001c0001t0004g0123a0001c0001t0013g0154others(1): Show | 4 | HG02258.hp1 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+5160C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513743 | ||||||
chr19:15513754
|
C | T | 1 | a0001c0001t0003g0303 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-109+5171C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513754 | ||||||
chr19:15513768
|
G | T | 1 | a0005c0006t0002g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-109+5185G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513768 | ||||||
chr19:15513912
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-109+5329G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15513912 | ||||||
chr19:15514074
|
T | G | 1 | a0001c0001t0002g0050 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-109+5491T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514074 | ||||||
chr19:15514237
|
T | G | 1 | a0001c0001t0001g0335 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-109+5654T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514237 | ||||||
chr19:15514361
|
T | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-109+5778T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514361 | ||||||
chr19:15514458
|
C | T | 2 | a0001c0001t0001g0340a0001c0001t0001g0357 | 2 | HG00323.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-109+5875C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514458 | ||||||
chr19:15514469
|
C | T | 146 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.-109+5886C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514469 | ||||||
chr19:15514488
|
C | T | 2 | a0002c0003t0002g0006a0002c0003t0002g0007 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-109+5905C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514488 | ||||||
chr19:15514844
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-109+6261C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514844 | ||||||
chr19:15514930
|
C | G | 1 | a0001c0001t0009g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+6347C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15514930 | ||||||
chr19:15515298
|
G | C | 1 | a0001c0001t0009g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-109+6715G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515298 | ||||||
chr19:15515315
|
A | G | 1 | a0001c0001t0005g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-109+6732A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515315 | ||||||
chr19:15515423
|
T | C | 1 | a0002c0003t0002g0362 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-109+6840T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515423 | ||||||
chr19:15515606
|
A | C | 4 | a0001c0001t0002g0325a0002c0003t0001g0323a0002c0003t0003g0004others(1): Show | 5 | HG02280.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-109+7023A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515606 | ||||||
chr19:15515705
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(21): Show | 24 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-109+7122A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515705 | ||||||
chr19:15515787
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0147others(133): Show | 138 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.-109+7204G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515787 | ||||||
chr19:15515792
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-109+7209C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515792 | ||||||
chr19:15515793
|
G | A | 2 | a0001c0001t0004g0090a0001c0001t0004g0091 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-109+7210G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515793 | ||||||
chr19:15515798
|
A | G | 1 | a0001c0001t0003g0001 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-109+7215A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515798 | ||||||
chr19:15515872
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-109+7289C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515872 | ||||||
chr19:15515875
|
C | T | 6 | a0001c0001t0001g0335a0001c0001t0001g0372a0001c0001t0002g0337others(3): Show | 6 | HG01123.hp1 HG01516.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.-109+7292C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515875 | ||||||
chr19:15515885
|
G | T | 1 | a0001c0002t0003g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-109+7302G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515885 | ||||||
chr19:15515913
|
T | C | 2 | a0001c0001t0002g0249a0001c0002t0003g0027 | 2 | HG01175.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-109+7330T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15515913 | ||||||
chr19:15516013
|
G | A | 20 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(17): Show | 20 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-109+7430G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516013 | ||||||
chr19:15516019
|
G | A | 3 | a0001c0001t0002g0098a0001c0001t0002g0104a0001c0001t0002g0132 | 3 | HG00408.hp1 NA18959.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-109+7436G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516019 | ||||||
chr19:15516047
|
A | C | 1 | a0001c0001t0001g0230 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-109+7464A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516047 | ||||||
chr19:15516135
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-109+7552G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516135 | ||||||
chr19:15516218
|
C | T | 2 | a0001c0001t0009g0011a0001c0005t0002g0015 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-108-7475C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516218 | ||||||
chr19:15516280
|
C | T | 2 | a0001c0001t0009g0011a0001c0005t0002g0015 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-108-7413C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516280 | ||||||
chr19:15516351
|
C | T | 3 | a0001c0001t0002g0177a0001c0001t0003g0174a0001c0001t0003g0291 | 3 | NA18990.hp2 NA18999.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-108-7342C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516351 | ||||||
chr19:15516397
|
A | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-108-7296A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516397 | ||||||
chr19:15516491
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0006g0172 | 2 | HG02738.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-108-7202C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516491 | ||||||
chr19:15516674
|
G | A | 1 | a0001c0001t0003g0133 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-108-7019G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516674 | ||||||
chr19:15516814
|
G | A | 1 | a0001c0001t0002g0003 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-108-6879G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516814 | ||||||
chr19:15516835
|
C | CT | 141 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0113others(138): Show | 143 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.-108-6839dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15516835 | |||||
chr19:15516835
|
CT | C | 6 | a0001c0001t0002g0050a0001c0001t0004g0090a0001c0001t0004g0091others(3): Show | 6 | HG02071.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-108-6839delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15516835 | |||||
chr19:15516858
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-108-6835A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516858 | ||||||
chr19:15516859
|
C | T | 157 | a0001c0001t0001g0002a0001c0001t0001g0113a0001c0001t0001g0147others(154): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-108-6834C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516859 | ||||||
chr19:15516950
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0004g0010others(3): Show | 6 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-6743C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15516950 | ||||||
chr19:15517012
|
G | A | 48 | a0001c0001t0001g0320a0001c0001t0001g0321a0001c0001t0001g0334others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.-108-6681G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517012 | ||||||
chr19:15517019
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-108-6674C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517019 | ||||||
chr19:15517064
|
G | A | 1 | a0002c0003t0003g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-108-6629G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517064 | ||||||
chr19:15517103
|
G | T | 1 | a0005c0006t0002g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-108-6590G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517103 | ||||||
chr19:15517116
|
C | T | 2 | a0002c0003t0002g0189a0006c0016t0005g0129 | 2 | HG01109.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-108-6577C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517116 | ||||||
chr19:15517161
|
A | AT | 179 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(176): Show | 181 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(178): Show |
intron_variant | MODIFIER | c.-108-6523dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15517161 | |||||
chr19:15517245
|
A | G | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-108-6448A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517245 | ||||||
chr19:15517250
|
C | A | 9 | a0001c0004t0001g0106a0001c0004t0001g0108a0001c0004t0001g0110others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-6443C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517250 | ||||||
chr19:15517260
|
T | C | 3 | a0001c0001t0002g0177a0001c0001t0003g0174a0001c0001t0003g0291 | 3 | NA18990.hp2 NA18999.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-108-6433T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517260 | ||||||
chr19:15517276
|
A | T | 1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-6417A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517276 | ||||||
chr19:15517402
|
C | T | 1 | a0001c0001t0004g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-108-6291C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517402 | ||||||
chr19:15517638
|
G | A | 8 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0020others(5): Show | 8 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-6055G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517638 | ||||||
chr19:15517641
|
T | C | 1 | a0001c0002t0002g0311 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-108-6052T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517641 | ||||||
chr19:15517908
|
C | T | 1 | a0002c0003t0002g0189 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-108-5785C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517908 | ||||||
chr19:15517974
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(134): Show | 139 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.-108-5719G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15517974 | ||||||
chr19:15518156
|
GCCAGACC others(9): Show |
G | 2 | a0001c0001t0001g0051a0001c0001t0001g0077 | 2 | NA18943.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.-108-5533_-108-551 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518156 | |||||
chr19:15518484
|
C | CA | 265 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0035others(262): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-108-5194dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518484 | |||||
chr19:15518484
|
C | CAA | 19 | a0001c0001t0001g0033a0001c0001t0001g0074a0001c0001t0001g0088others(16): Show | 19 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-108-5195_-108-519 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518484 | |||||
chr19:15518496
|
A | ATAT | 9 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(6): Show | 9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-5197_-108-519 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518496 | ||||||
chr19:15518498
|
A | AAAT | 9 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0020others(6): Show | 9 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-5194_-108-519 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518498 | |||||
chr19:15518498
|
A | ATAT | 8 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0004g0010others(5): Show | 8 | HG02622.hp1 HG02922.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108-5195_-108-519 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518498 | ||||||
chr19:15518498
|
A | T | 9 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(6): Show | 9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-5195A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518498 | ||||||
chr19:15518603
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0376a0001c0001t0002g0013others(14): Show | 17 | HG02109.hp1 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.-108-5090C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518603 | ||||||
chr19:15518647
|
C | CA | 45 | a0001c0001t0001g0122a0001c0001t0001g0165a0001c0001t0001g0170others(42): Show | 46 | HG00621.hp1 HG00741.hp1 HG01358.hp1 others(43): Show |
intron_variant | MODIFIER | c.-108-5024dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | |||||
chr19:15518647
|
C | CAA | 12 | a0001c0001t0002g0068a0001c0001t0002g0127a0001c0001t0003g0300others(9): Show | 12 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108-5025_-108-502 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | |||||
chr19:15518647
|
C | CAAA | 8 | a0001c0004t0001g0108a0001c0004t0001g0110a0001c0004t0001g0140others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-5026_-108-502 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | |||||
chr19:15518647
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-108-5046C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518647 | ||||||
chr19:15518647
|
CA | C | 10 | a0001c0001t0001g0058a0001c0001t0002g0013a0001c0001t0002g0155others(7): Show | 10 | HG01099.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-5024delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | |||||
chr19:15518647
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-108-5033_-108-502 others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518647 | |||||
chr19:15518688
|
GA | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0165others(33): Show | 36 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-108-4991delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518688 | |||||
chr19:15518698
|
A | G | 4 | a0001c0001t0002g0155a0001c0001t0004g0128a0001c0001t0004g0168others(1): Show | 4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-4995A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518698 | ||||||
chr19:15518718
|
CAA | C | 8 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0020others(5): Show | 8 | HG00621.hp2 HG01891.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-108-4972_-108-497 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15518718 | |||||
chr19:15518782
|
G | T | 1 | a0001c0001t0002g0271 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-108-4911G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518782 | ||||||
chr19:15518858
|
T | C | 328 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(325): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-108-4835T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15518858 | ||||||
chr19:15519008
|
G | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0002g0013others(29): Show | 32 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-108-4685G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519008 | ||||||
chr19:15519019
|
G | C | 7 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(4): Show | 7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-4674G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519019 | ||||||
chr19:15519141
|
C | T | 1 | a0002c0003t0003g0167 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-108-4552C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519141 | ||||||
chr19:15519172
|
C | T | 4 | a0001c0001t0002g0155a0001c0001t0004g0128a0001c0001t0004g0168others(1): Show | 4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-4521C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519172 | ||||||
chr19:15519181
|
G | C | 3 | a0001c0001t0001g0365a0001c0001t0003g0366a0001c0001t0003g0369 | 3 | HG00099.hp2 HG01069.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-108-4512G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519181 | ||||||
chr19:15519211
|
A | G | 2 | a0001c0001t0009g0011a0001c0005t0002g0015 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-108-4482A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519211 | ||||||
chr19:15519262
|
G | GA | 3 | a0001c0001t0001g0310a0001c0001t0002g0045a0001c0001t0006g0145 | 3 | HG02080.hp1 NA18991.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.-108-4430dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15519262 | |||||
chr19:15519263
|
A | AT | 17 | a0001c0001t0001g0094a0001c0001t0001g0135a0001c0001t0001g0165others(14): Show | 17 | HG01109.hp1 HG01192.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-108-4413dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15519263 | |||||
chr19:15519264
|
T | A | 164 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0030others(161): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-108-4429T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519264 | ||||||
chr19:15519302
|
A | G | 331 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(328): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-108-4391A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519302 | ||||||
chr19:15519407
|
C | T | 144 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(141): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.-108-4286C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519407 | ||||||
chr19:15519465
|
G | T | 2 | a0001c0001t0002g0103a0001c0001t0003g0171 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-108-4228G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519465 | ||||||
chr19:15519475
|
C | G | 1 | a0001c0001t0002g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-108-4218C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519475 | ||||||
chr19:15519493
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0002g0020others(6): Show | 9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-4200C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519493 | ||||||
chr19:15519578
|
T | C | 143 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.-108-4115T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519578 | ||||||
chr19:15519642
|
G | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(130): Show | 135 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.-108-4051G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519642 | ||||||
chr19:15519787
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-108-3906A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519787 | ||||||
chr19:15519864
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-108-3829C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519864 | ||||||
chr19:15519872
|
T | C | 3 | a0001c0001t0004g0231a0001c0001t0009g0011a0001c0005t0002g0015 | 3 | HG02257.hp1 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-108-3821T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15519872 | ||||||
chr19:15520071
|
G | T | 2 | a0001c0001t0004g0090a0001c0001t0004g0091 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-108-3622G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520071 | ||||||
chr19:15520115
|
C | T | 1 | a0001c0001t0002g0326 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-108-3578C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520115 | ||||||
chr19:15520218
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0204 | 2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.-108-3475C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520218 | ||||||
chr19:15520219
|
G | A | 10 | a0001c0001t0001g0151a0001c0001t0002g0066a0001c0001t0002g0068others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-3474G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520219 | ||||||
chr19:15520310
|
T | C | 1 | a0001c0012t0002g0220 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-108-3383T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520310 | ||||||
chr19:15520325
|
G | A | 1 | a0001c0012t0002g0220 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-108-3368G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520325 | ||||||
chr19:15520327
|
C | T | 1 | a0001c0012t0002g0220 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-108-3366C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520327 | ||||||
chr19:15520336
|
C | A | 1 | a0001c0012t0002g0220 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-108-3357C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520336 | ||||||
chr19:15520345
|
C | CA | 71 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0001g0130others(68): Show | 71 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.-108-3332dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520345 | |||||
chr19:15520356
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-108-3337A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520356 | ||||||
chr19:15520362
|
C | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(150): Show | 155 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.-108-3331C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520362 | ||||||
chr19:15520402
|
G | GT | 138 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(135): Show | 140 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.-108-3280dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520402 | |||||
chr19:15520402
|
G | GTT | 7 | a0001c0001t0001g0269a0001c0001t0001g0279a0001c0001t0001g0280others(4): Show | 7 | HG02074.hp1 NA18945.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-3281_-108-328 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520402 | |||||
chr19:15520552
|
G | A | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-108-3141G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520552 | ||||||
chr19:15520681
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0002g0020others(6): Show | 9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-3012A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520681 | ||||||
chr19:15520687
|
A | G | 1 | a0001c0001t0002g0316 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-108-3006A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520687 | ||||||
chr19:15520719
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-108-2974C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520719 | ||||||
chr19:15520727
|
A | G | 15 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-2966A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520727 | ||||||
chr19:15520761
|
G | GT | 5 | a0001c0001t0001g0057a0001c0001t0002g0258a0001c0001t0004g0090others(2): Show | 5 | HG02074.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-2928dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520761 | |||||
chr19:15520763
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-108-2930T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520763 | ||||||
chr19:15520766
|
G | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(132): Show | 137 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.-108-2927G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520766 | ||||||
chr19:15520774
|
G | GT | 12 | a0001c0001t0001g0074a0001c0001t0001g0094a0001c0001t0001g0134others(9): Show | 12 | HG00621.hp1 HG00741.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.-108-2907dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520774 | |||||
chr19:15520774
|
GT | G | 17 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(14): Show | 17 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-108-2907delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15520774 | |||||
chr19:15520957
|
C | T | 2 | a0002c0003t0002g0006a0002c0003t0002g0007 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-108-2736C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15520957 | ||||||
chr19:15521052
|
C | T | 1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-2641C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521052 | ||||||
chr19:15521231
|
C | CT | 23 | a0001c0001t0001g0026a0001c0001t0001g0135a0001c0001t0001g0210others(20): Show | 23 | HG00621.hp2 HG00741.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.-108-2444dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15521231 | |||||
chr19:15521231
|
CT | C | 168 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0033others(165): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.-108-2444delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15521231 | |||||
chr19:15521262
|
C | T | 143 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.-108-2431C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521262 | ||||||
chr19:15521421
|
C | T | 2 | a0001c0001t0009g0011a0001c0005t0002g0015 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-108-2272C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521421 | ||||||
chr19:15521524
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0002g0020others(6): Show | 9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-108-2169G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521524 | ||||||
chr19:15521755
|
C | T | 1 | a0001c0001t0005g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-108-1938C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521755 | ||||||
chr19:15521824
|
C | G | 6 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0004g0010others(3): Show | 6 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-108-1869C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521824 | ||||||
chr19:15521834
|
C | A | 130 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-108-1859C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521834 | ||||||
chr19:15521878
|
C | T | 1 | a0003c0008t0004g0378 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-108-1815C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521878 | ||||||
chr19:15521882
|
C | T | 10 | a0001c0001t0001g0151a0001c0001t0002g0066a0001c0001t0002g0068others(7): Show | 10 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-1811C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521882 | ||||||
chr19:15521942
|
C | T | 1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-1751C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521942 | ||||||
chr19:15521961
|
A | G | 10 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-108-1732A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15521961 | ||||||
chr19:15522022
|
A | G | 4 | a0001c0001t0002g0155a0001c0001t0004g0128a0001c0001t0004g0168others(1): Show | 4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-1671A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522022 | ||||||
chr19:15522147
|
GA | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(128): Show | 133 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.-108-1527delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 15522147 | |||||
chr19:15522573
|
G | A | 1 | a0001c0001t0005g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-108-1120G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522573 | ||||||
chr19:15522625
|
G | A | 141 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-108-1068G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522625 | ||||||
chr19:15522666
|
G | A | 8 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(5): Show | 8 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108-1027G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522666 | ||||||
chr19:15522724
|
G | T | 2 | a0001c0001t0001g0156a0001c0001t0002g0169 | 2 | NA18977.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-108-969G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522724 | ||||||
chr19:15522734
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-108-959G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522734 | ||||||
chr19:15522745
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-108-948C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522745 | ||||||
chr19:15522773
|
C | T | 15 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(12): Show | 15 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-108-920C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522773 | ||||||
chr19:15522872
|
G | A | 1 | a0001c0002t0003g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-108-821G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522872 | ||||||
chr19:15522934
|
C | T | 1 | a0006c0017t0002g0368 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-108-759C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522934 | ||||||
chr19:15522962
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-108-731C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15522962 | ||||||
chr19:15523130
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-108-563G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523130 | ||||||
chr19:15523314
|
C | T | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-379C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523314 | ||||||
chr19:15523534
|
G | A | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-108-159G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523534 | ||||||
chr19:15523653
|
A | G | 1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-40A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523653 | ||||||
chr19:15523654
|
A | G | 8 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(5): Show | 8 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.-108-39A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523654 | ||||||
chr19:15523671
|
C | A | 1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-108-22C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 1/13 | chr19 | 15523671 | ||||||
chr19:15524064
|
G | GA | 134 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(131): Show | 136 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.-2+279dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524064 | |||||
chr19:15524064
|
GA | G | 8 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(5): Show | 8 | HG00621.hp2 HG02965.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2+279delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524064 | |||||
chr19:15524208
|
G | T | 2 | a0001c0005t0004g0017a0001c0005t0004g0018 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-2+409G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524208 | ||||||
chr19:15524372
|
G | A | 2 | a0001c0001t0002g0066a0001c0001t0003g0065 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-2+573G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524372 | ||||||
chr19:15524409
|
G | A | 2 | a0001c0001t0009g0011a0001c0005t0002g0015 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-2+610G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524409 | ||||||
chr19:15524640
|
C | A | 1 | a0001c0001t0002g0380 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-1-696C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524640 | ||||||
chr19:15524669
|
G | GGA | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-654_-1-653dupGA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524669 | |||||
chr19:15524680
|
G | GAGAA | 148 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0033others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-1-636_-1-633dupAA others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524680 | |||||
chr19:15524680
|
GAGAA | G | 10 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0002g0020others(7): Show | 10 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-636_-1-633delAA others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr19 | 15524680 | |||||
chr19:15524700
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0002g0020others(6): Show | 9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-636A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524700 | ||||||
chr19:15524708
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0002g0020others(6): Show | 9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-628G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15524708 | ||||||
chr19:15525148
|
C | T | 2 | a0001c0001t0004g0090a0001c0001t0004g0091 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-1-188C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15525148 | ||||||
chr19:15525283
|
A | G | 4 | a0001c0001t0002g0155a0001c0001t0004g0128a0001c0001t0004g0168others(1): Show | 4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-53A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15525283 | ||||||
chr19:15525307
|
A | G | 13 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(10): Show | 13 | HG02109.hp1 HG02109.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-1-29A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15525307 | ||||||
chr19:15525310
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-1-26G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 2/13 | chr19 | 15525310 | ||||||
chr19:15525626
|
T | C | 7 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(4): Show | 7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+68T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15525626 | ||||||
chr19:15525694
|
G | C | 1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.222+136G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15525694 | ||||||
chr19:15525871
|
T | A | 177 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0030others(174): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.222+313T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15525871 | ||||||
chr19:15525959
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0234a0001c0001t0003g0238 | 3 | NA18950.hp2 NA18957.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.222+401C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15525959 | ||||||
chr19:15526127
|
C | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(126): Show | 131 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.222+569C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526127 | ||||||
chr19:15526240
|
T | A | 5 | a0001c0001t0001g0047a0001c0001t0002g0028a0001c0001t0002g0036others(2): Show | 5 | NA18612.hp1 NA18946.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+682T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526240 | ||||||
chr19:15526295
|
T | C | 7 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(4): Show | 7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+737T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526295 | ||||||
chr19:15526347
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0002g0101 | 2 | HG02083.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.222+789C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526347 | ||||||
chr19:15526520
|
C | A | 8 | a0001c0001t0001g0151a0001c0001t0002g0066a0001c0001t0002g0068others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+962C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526520 | ||||||
chr19:15526565
|
GC | G | 8 | a0001c0001t0001g0151a0001c0001t0002g0066a0001c0001t0002g0068others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+1008delC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526565 | ||||||
chr19:15526747
|
C | CT | 10 | a0001c0001t0001g0207a0001c0001t0001g0376a0001c0001t0002g0380others(7): Show | 10 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+1205dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15526747 | |||||
chr19:15526765
|
G | A | 1 | a0001c0001t0001g0281 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.222+1207G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526765 | ||||||
chr19:15526783
|
T | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0376others(25): Show | 28 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.222+1225T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526783 | ||||||
chr19:15526906
|
C | T | 9 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(6): Show | 9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+1348C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15526906 | ||||||
chr19:15527008
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.222+1450C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527008 | ||||||
chr19:15527111
|
C | T | 1 | a0001c0001t0008g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.222+1553C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527111 | ||||||
chr19:15527195
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0002g0020others(6): Show | 9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.222+1637G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527195 | ||||||
chr19:15527218
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.222+1660G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527218 | ||||||
chr19:15527266
|
G | A | 1 | a0012c0019t0001g0046 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.222+1708G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527266 | ||||||
chr19:15527327
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.222+1769T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527327 | ||||||
chr19:15527331
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.222+1773C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527331 | ||||||
chr19:15527454
|
A | G | 1 | a0001c0001t0002g0254 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.222+1896A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527454 | ||||||
chr19:15527676
|
A | G | 28 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0376others(25): Show | 28 | HG00621.hp2 HG01891.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.223-2033A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527676 | ||||||
chr19:15527689
|
C | T | 19 | a0001c0001t0001g0078a0001c0001t0001g0087a0001c0001t0001g0310others(16): Show | 19 | HG00408.hp2 HG00673.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.223-2020C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527689 | ||||||
chr19:15527726
|
G | T | 9 | a0001c0001t0001g0005a0001c0001t0002g0013a0001c0001t0002g0020others(6): Show | 9 | HG01891.hp2 HG02622.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.223-1983G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527726 | ||||||
chr19:15527747
|
T | A | 7 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(4): Show | 7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.223-1962T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527747 | ||||||
chr19:15527863
|
C | T | 1 | a0001c0001t0004g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223-1846C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527863 | ||||||
chr19:15527951
|
C | A | 1 | a0001c0001t0002g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.223-1758C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15527951 | ||||||
chr19:15528172
|
GCTGGGCA others(8): Show |
G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | NA18948.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.223-1535_223-1521d others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15528172 | |||||
chr19:15528207
|
C | T | 8 | a0001c0001t0001g0151a0001c0001t0002g0066a0001c0001t0002g0068others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-1502C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528207 | ||||||
chr19:15528263
|
G | A | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.223-1446G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528263 | ||||||
chr19:15528422
|
T | C | 1 | a0001c0002t0002g0311 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223-1287T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528422 | ||||||
chr19:15528457
|
T | C | 1 | a0001c0001t0002g0306 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.223-1252T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528457 | ||||||
chr19:15528484
|
A | G | 8 | a0001c0001t0001g0151a0001c0001t0002g0066a0001c0001t0002g0068others(5): Show | 8 | HG02055.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.223-1225A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528484 | ||||||
chr19:15528530
|
T | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(138): Show | 143 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.223-1179T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528530 | ||||||
chr19:15528569
|
GTCT | G | 132 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.223-1134_223-1132d others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15528569 | |||||
chr19:15528788
|
A | T | 1 | a0001c0002t0003g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.223-921A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528788 | ||||||
chr19:15528904
|
A | G | 153 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0033others(150): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.223-805A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528904 | ||||||
chr19:15528930
|
T | C | 1 | a0001c0002t0002g0311 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223-779T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15528930 | ||||||
chr19:15529117
|
C | T | 1 | a0002c0003t0002g0362 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.223-592C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529117 | ||||||
chr19:15529133
|
A | AT | 26 | a0001c0001t0001g0376a0001c0001t0002g0066a0001c0001t0002g0068others(23): Show | 26 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.223-564dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15529133 | |||||
chr19:15529133
|
A | ATT | 161 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(158): Show | 163 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.223-565_223-564dup others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15529133 | |||||
chr19:15529133
|
A | ATTT | 7 | a0001c0001t0001g0203a0001c0001t0003g0300a0001c0001t0003g0301others(4): Show | 7 | HG00621.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-566_223-564dup others(3): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15529133 | |||||
chr19:15529136
|
T | TTA | 141 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(138): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.223-572_223-571ins others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr19 | 15529136 | |||||
chr19:15529185
|
A | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0058others(139): Show | 144 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.223-524A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529185 | ||||||
chr19:15529197
|
C | T | 1 | a0001c0001t0002g0244 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.223-512C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529197 | ||||||
chr19:15529349
|
G | A | 2 | a0002c0003t0002g0006a0002c0003t0002g0007 | 2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.223-360G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529349 | ||||||
chr19:15529477
|
G | T | 134 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.223-232G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529477 | ||||||
chr19:15529596
|
C | T | 1 | a0011c0014t0011g0288 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.223-113C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 3/13 | chr19 | 15529596 | ||||||
chr19:15529858
|
G | A | 7 | a0001c0001t0001g0026a0001c0001t0002g0019a0001c0001t0002g0021others(4): Show | 7 | HG00621.hp2 HG02965.hp1 HG03491.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.367+5G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15529858 | ||||||
chr19:15530161
|
G | A | 183 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0033others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.367+308G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530161 | ||||||
chr19:15530167
|
C | T | 1 | a0009c0015t0004g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.367+314C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530167 | ||||||
chr19:15530219
|
C | T | 137 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0035others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.367+366C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530219 | ||||||
chr19:15530314
|
C | T | 1 | a0001c0001t0009g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.367+461C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530314 | ||||||
chr19:15530384
|
C | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0030others(290): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.367+531C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530384 | ||||||
chr19:15530386
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.367+533C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530386 | ||||||
chr19:15530531
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.367+678T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530531 | ||||||
chr19:15530578
|
T | C | 1 | a0001c0001t0003g0148 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.367+725T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530578 | ||||||
chr19:15530643
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0006g0145 | 2 | NA18945.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.367+790C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530643 | ||||||
chr19:15530653
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.367+800G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530653 | ||||||
chr19:15530705
|
C | A | 1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.367+852C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530705 | ||||||
chr19:15530938
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0006g0029 | 3 | HG01257.hp2 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.367+1085A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15530938 | ||||||
chr19:15531025
|
T | C | 1 | a0002c0003t0005g0328 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.367+1172T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531025 | ||||||
chr19:15531126
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0277a0001c0001t0001g0350 | 3 | HG00673.hp2 HG02080.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.367+1273C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531126 | ||||||
chr19:15531202
|
C | T | 19 | a0001c0001t0001g0035a0001c0001t0001g0121a0001c0001t0001g0122others(16): Show | 20 | HG00639.hp2 HG00642.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.367+1349C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531202 | ||||||
chr19:15531206
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.367+1353A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531206 | ||||||
chr19:15531283
|
G | C | 1 | a0005c0006t0002g0327 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.367+1430G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531283 | ||||||
chr19:15531308
|
A | C | 2 | a0001c0001t0001g0002a0001c0001t0002g0217 | 3 | NA18948.hp2 NA19010.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.367+1455A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531308 | ||||||
chr19:15531321
|
A | T | 1 | a0001c0002t0003g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.367+1468A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531321 | ||||||
chr19:15531378
|
G | T | 5 | a0001c0001t0001g0340a0001c0001t0001g0356a0001c0001t0001g0357others(2): Show | 5 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(2): Show |
intron_variant | MODIFIER | c.367+1525G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531378 | ||||||
chr19:15531384
|
T | TA | 72 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0033others(69): Show | 72 | HG00408.hp2 HG00673.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.367+1546dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15531384 | |||||
chr19:15531384
|
T | TAA | 225 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0057others(222): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.367+1545_367+1546d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15531384 | |||||
chr19:15531384
|
T | TAAA | 38 | a0001c0001t0001g0035a0001c0001t0001g0121a0001c0001t0001g0122others(35): Show | 39 | HG00639.hp2 HG00642.hp2 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.367+1544_367+1546d others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15531384 | |||||
chr19:15531433
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.367+1580C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531433 | ||||||
chr19:15531455
|
G | A | 2 | a0001c0001t0003g0162a0001c0005t0002g0015 | 2 | HG01175.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.367+1602G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531455 | ||||||
chr19:15531483
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.367+1630A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531483 | ||||||
chr19:15531663
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.367+1810A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531663 | ||||||
chr19:15531764
|
G | A | 4 | a0001c0001t0002g0155a0001c0001t0004g0128a0001c0001t0004g0168others(1): Show | 4 | HG01934.hp2 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+1911G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15531764 | ||||||
chr19:15532114
|
T | TA | 14 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0151others(11): Show | 14 | HG01934.hp1 HG01934.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.367+2271dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15532114 | |||||
chr19:15532463
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.367+2610C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532463 | ||||||
chr19:15532497
|
C | T | 39 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0121others(36): Show | 40 | HG00639.hp2 HG00642.hp2 HG01934.hp2 others(37): Show |
intron_variant | MODIFIER | c.367+2644C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532497 | ||||||
chr19:15532549
|
AT | A | 19 | a0001c0001t0001g0035a0001c0001t0001g0121a0001c0001t0001g0122others(16): Show | 20 | HG00639.hp2 HG00642.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.367+2707delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15532549 | |||||
chr19:15532571
|
G | A | 2 | a0001c0001t0002g0103a0001c0001t0003g0171 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.367+2718G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532571 | ||||||
chr19:15532679
|
GTC | G | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+2832_367+2833d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15532679 | |||||
chr19:15532714
|
C | T | 4 | a0001c0001t0003g0296a0001c0001t0003g0297a0001c0001t0003g0298others(1): Show | 4 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+2861C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532714 | ||||||
chr19:15532718
|
C | G | 9 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(6): Show | 9 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+2865C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532718 | ||||||
chr19:15532779
|
G | A | 126 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0055others(123): Show | 127 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.367+2926G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532779 | ||||||
chr19:15532780
|
A | C | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.367+2927A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532780 | ||||||
chr19:15532859
|
A | G | 49 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0121others(46): Show | 50 | HG00639.hp2 HG00642.hp2 HG01934.hp2 others(47): Show |
intron_variant | MODIFIER | c.367+3006A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532859 | ||||||
chr19:15532869
|
C | T | 40 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0121others(37): Show | 41 | HG00639.hp2 HG00642.hp2 HG01934.hp2 others(38): Show |
intron_variant | MODIFIER | c.367+3016C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15532869 | ||||||
chr19:15533043
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0002g0013others(19): Show | 22 | HG01934.hp2 HG02257.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.367+3190G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533043 | ||||||
chr19:15533187
|
A | G | 1 | a0001c0001t0004g0371 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.367+3334A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533187 | ||||||
chr19:15533372
|
TA | T | 9 | a0001c0004t0001g0106a0001c0004t0001g0108a0001c0004t0001g0110others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+3526delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533372 | |||||
chr19:15533379
|
A | T | 9 | a0001c0004t0001g0106a0001c0004t0001g0108a0001c0004t0001g0110others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+3526A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533379 | ||||||
chr19:15533428
|
C | T | 1 | a0001c0001t0004g0355 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.367+3575C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533428 | ||||||
chr19:15533591
|
C | CT | 113 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0033others(110): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.368-3748dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533591 | |||||
chr19:15533591
|
C | CTT | 23 | a0001c0001t0001g0035a0001c0001t0001g0121a0001c0001t0001g0367others(20): Show | 24 | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.368-3749_368-3748d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533591 | |||||
chr19:15533591
|
C | CTTT | 13 | a0001c0001t0001g0005a0001c0001t0001g0122a0001c0001t0001g0151others(10): Show | 13 | HG00642.hp2 HG01978.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.368-3750_368-3748d others(5): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533591 | |||||
chr19:15533591
|
CT | C | 6 | a0001c0001t0001g0235a0001c0001t0002g0061a0001c0001t0002g0099others(3): Show | 6 | HG01168.hp1 HG02897.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-3748delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 15533591 | |||||
chr19:15533618
|
C | T | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368-3743C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533618 | ||||||
chr19:15533622
|
G | T | 1 | a0001c0001t0003g0023 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.368-3739G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533622 | ||||||
chr19:15533648
|
A | G | 4 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-3713A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533648 | ||||||
chr19:15533725
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.368-3636C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15533725 | ||||||
chr19:15534018
|
G | A | 6 | a0001c0001t0009g0011a0001c0002t0003g0008a0001c0005t0002g0015others(3): Show | 6 | HG02257.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-3343G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534018 | ||||||
chr19:15534045
|
G | A | 2 | a0001c0001t0002g0103a0001c0001t0002g0295 | 2 | HG01358.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.368-3316G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534045 | ||||||
chr19:15534128
|
T | C | 11 | a0001c0001t0001g0035a0001c0001t0001g0121a0001c0001t0001g0122others(8): Show | 12 | HG00639.hp2 HG00642.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-3233T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534128 | ||||||
chr19:15534250
|
T | C | 2 | a0001c0001t0002g0306a0001c0001t0002g0307 | 2 | NA19064.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.368-3111T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534250 | ||||||
chr19:15534454
|
A | G | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368-2907A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534454 | ||||||
chr19:15534605
|
T | C | 205 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0035others(202): Show | 207 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.368-2756T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534605 | ||||||
chr19:15534656
|
G | A | 330 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(327): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.368-2705G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534656 | ||||||
chr19:15534809
|
C | T | 335 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.368-2552C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534809 | ||||||
chr19:15534958
|
G | A | 10 | a0001c0004t0001g0106a0001c0004t0001g0108a0001c0004t0001g0110others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.368-2403G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15534958 | ||||||
chr19:15535045
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.368-2316C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535045 | ||||||
chr19:15535098
|
G | T | 1 | a0001c0005t0002g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.368-2263G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535098 | ||||||
chr19:15535154
|
A | G | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368-2207A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535154 | ||||||
chr19:15535213
|
A | T | 2 | a0001c0001t0001g0309a0001c0001t0003g0308 | 2 | NA18980.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.368-2148A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535213 | ||||||
chr19:15535240
|
G | A | 19 | a0001c0001t0001g0035a0001c0001t0001g0121a0001c0001t0001g0122others(16): Show | 20 | HG00639.hp2 HG00642.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.368-2121G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535240 | ||||||
chr19:15535384
|
A | T | 1 | a0001c0002t0003g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.368-1977A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535384 | ||||||
chr19:15535434
|
G | T | 340 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(337): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.368-1927G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535434 | ||||||
chr19:15535557
|
T | C | 1 | a0001c0001t0002g0314 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.368-1804T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535557 | ||||||
chr19:15535671
|
T | C | 162 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0055others(159): Show | 163 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.368-1690T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535671 | ||||||
chr19:15535860
|
G | A | 2 | a0001c0001t0004g0185a0001c0001t0004g0186 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.368-1501G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15535860 | ||||||
chr19:15536041
|
A | C | 1 | a0001c0002t0003g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.368-1320A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536041 | ||||||
chr19:15536159
|
C | T | 49 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0033others(46): Show | 50 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.368-1202C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536159 | ||||||
chr19:15536361
|
A | C | 6 | a0001c0001t0002g0127a0001c0001t0002g0326a0001c0001t0004g0089others(3): Show | 6 | HG01934.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-1000A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536361 | ||||||
chr19:15536381
|
C | T | 52 | a0001c0001t0001g0193a0001c0001t0001g0216a0001c0001t0001g0261others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.368-980C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536381 | ||||||
chr19:15536391
|
G | C | 163 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0055others(160): Show | 164 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(161): Show |
intron_variant | MODIFIER | c.368-970G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536391 | ||||||
chr19:15536483
|
G | C | 13 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0003g0303others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.368-878G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536483 | ||||||
chr19:15536500
|
C | T | 1 | a0001c0001t0004g0371 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.368-861C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536500 | ||||||
chr19:15536559
|
G | A | 2 | a0001c0001t0002g0127a0001c0001t0004g0089 | 2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.368-802G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536559 | ||||||
chr19:15536578
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.368-783G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536578 | ||||||
chr19:15536824
|
T | G | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.368-537T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536824 | ||||||
chr19:15536831
|
A | G | 11 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(8): Show | 11 | HG02109.hp1 HG02109.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.368-530A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536831 | ||||||
chr19:15536848
|
T | G | 2 | a0001c0005t0004g0017a0001c0005t0004g0018 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.368-513T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536848 | ||||||
chr19:15536968
|
G | A | 1 | a0001c0001t0002g0031 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.368-393G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15536968 | ||||||
chr19:15537035
|
G | A | 10 | a0001c0001t0007g0322a0002c0003t0001g0323a0002c0003t0002g0362others(7): Show | 11 | HG02280.hp1 HG02451.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-326G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537035 | ||||||
chr19:15537072
|
G | A | 41 | a0001c0001t0001g0122a0001c0001t0001g0216a0001c0001t0001g0261others(38): Show | 41 | HG00099.hp2 HG00280.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.368-289G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537072 | ||||||
chr19:15537144
|
C | G | 1 | a0001c0001t0004g0016 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.368-217C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537144 | ||||||
chr19:15537162
|
A | G | 2 | a0001c0001t0002g0155a0001c0001t0004g0128 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.368-199A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537162 | ||||||
chr19:15537176
|
C | T | 1 | a0001c0001t0005g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.368-185C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537176 | ||||||
chr19:15537185
|
C | T | 77 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0047others(74): Show | 77 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.368-176C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537185 | ||||||
chr19:15537279
|
T | C | 2 | a0001c0001t0009g0011a0001c0004t0002g0173 | 2 | HG02559.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.368-82T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537279 | ||||||
chr19:15537314
|
C | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0002g0013others(5): Show | 8 | HG02559.hp1 HG02622.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.368-47C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537314 | ||||||
chr19:15537337
|
C | T | 149 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0052others(146): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.368-24C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537337 | ||||||
chr19:15537352
|
C | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0002g0013others(4): Show | 7 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.368-9C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 4/13 | chr19 | 15537352 | ||||||
chr19:15537490
|
T | A | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.422-45T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 5/13 | chr19 | 15537490 | ||||||
chr19:15537807
|
G | T | 1 | a0001c0001t0003g0266 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.550-65G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 6/13 | chr19 | 15537807 | ||||||
chr19:15538056
|
G | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0230others(23): Show | 27 | HG00621.hp2 HG00639.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.671+63G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538056 | ||||||
chr19:15538158
|
T | C | 6 | a0001c0001t0001g0147a0001c0001t0001g0207a0001c0001t0001g0235others(3): Show | 6 | HG00735.hp2 HG02004.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.671+165T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538158 | ||||||
chr19:15538192
|
C | T | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.671+199C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538192 | ||||||
chr19:15538336
|
G | A | 2 | a0001c0001t0003g0162a0001c0001t0003g0358 | 2 | HG01167.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.671+343G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538336 | ||||||
chr19:15538392
|
A | T | 7 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.671+399A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538392 | ||||||
chr19:15538473
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.671+480A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538473 | ||||||
chr19:15538482
|
G | A | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.671+489G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538482 | ||||||
chr19:15538635
|
G | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0086others(53): Show | 57 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.671+642G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538635 | ||||||
chr19:15538698
|
G | A | 267 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(264): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.671+705G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538698 | ||||||
chr19:15538723
|
G | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0230others(24): Show | 28 | HG00621.hp2 HG00639.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.671+730G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15538723 | ||||||
chr19:15539301
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.672-1149T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539301 | ||||||
chr19:15539354
|
G | A | 331 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(328): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.672-1096G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539354 | ||||||
chr19:15539451
|
C | T | 355 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(352): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.672-999C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539451 | ||||||
chr19:15539465
|
C | T | 2 | a0002c0003t0004g0329a0002c0003t0004g0330 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.672-985C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539465 | ||||||
chr19:15539502
|
A | G | 1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.672-948A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539502 | ||||||
chr19:15539543
|
A | G | 1 | a0001c0004t0004g0107 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.672-907A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539543 | ||||||
chr19:15539574
|
C | T | 323 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(320): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.672-876C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15539574 | ||||||
chr19:15540150
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.672-300G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15540150 | ||||||
chr19:15540281
|
G | A | 7 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.672-169G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15540281 | ||||||
chr19:15540403
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0074 | 3 | HG01515.hp1 HG01517.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.672-47A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 7/13 | chr19 | 15540403 | ||||||
chr19:15540728
|
GCC | G | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+15_939+16delCC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15540728 | |||||
chr19:15540737
|
A | AG | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+20_939+21insG | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540737 | ||||||
chr19:15540738
|
A | G | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+21A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540738 | ||||||
chr19:15540739
|
T | G | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+22T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540739 | ||||||
chr19:15540742
|
C | G | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+25C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540742 | ||||||
chr19:15540743
|
T | A | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+26T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540743 | ||||||
chr19:15540745
|
G | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+28G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540745 | ||||||
chr19:15540749
|
C | G | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+32C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540749 | ||||||
chr19:15540751
|
CG | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+35delG | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540751 | ||||||
chr19:15540753
|
A | T | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+36A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540753 | ||||||
chr19:15540757
|
C | A | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+40C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540757 | ||||||
chr19:15540805
|
T | G | 1 | a0001c0001t0001g0178 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.939+88T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540805 | ||||||
chr19:15540811
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.939+94G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540811 | ||||||
chr19:15540864
|
C | T | 7 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.939+147C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540864 | ||||||
chr19:15540881
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.939+164T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540881 | ||||||
chr19:15540917
|
T | G | 5 | a0001c0001t0002g0066a0001c0001t0002g0180a0001c0001t0002g0232others(2): Show | 5 | HG02145.hp2 HG02559.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+200T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540917 | ||||||
chr19:15540920
|
A | G | 4 | a0002c0003t0004g0329a0002c0003t0004g0330a0002c0003t0005g0315others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.939+203A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540920 | ||||||
chr19:15540960
|
G | A | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+243G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540960 | ||||||
chr19:15540979
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.939+262G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540979 | ||||||
chr19:15540991
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.939+274G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15540991 | ||||||
chr19:15541079
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.939+362C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541079 | ||||||
chr19:15541135
|
C | G | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+418C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541135 | ||||||
chr19:15541267
|
A | G | 34 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0052others(31): Show | 34 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.939+550A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541267 | ||||||
chr19:15541395
|
T | C | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.939+678T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541395 | ||||||
chr19:15541537
|
G | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0086others(62): Show | 66 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.939+820G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541537 | ||||||
chr19:15541538
|
G | C | 1 | a0001c0001t0001g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.939+821G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541538 | ||||||
chr19:15541539
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.939+822G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541539 | ||||||
chr19:15541547
|
G | C | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+830G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541547 | ||||||
chr19:15541548
|
C | A | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+831C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541548 | ||||||
chr19:15541549
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+832A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541549 | ||||||
chr19:15541737
|
G | A | 5 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0001g0094others(2): Show | 5 | NA18946.hp1 NA18955.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.939+1020G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541737 | ||||||
chr19:15541737
|
G | T | 5 | a0001c0001t0002g0066a0001c0001t0002g0180a0001c0001t0002g0232others(2): Show | 5 | HG02145.hp2 HG02559.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+1020G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541737 | ||||||
chr19:15541742
|
T | C | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1025T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541742 | ||||||
chr19:15541804
|
TG | T | 7 | a0001c0001t0001g0372a0001c0001t0002g0127a0001c0001t0002g0155others(4): Show | 7 | HG01123.hp1 HG01884.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.939+1090delG | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15541804 | |||||
chr19:15541831
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0086others(58): Show | 62 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.939+1114G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541831 | ||||||
chr19:15541861
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0230others(25): Show | 29 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.939+1144G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541861 | ||||||
chr19:15541865
|
C | CA | 89 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0047others(86): Show | 91 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.939+1166dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15541865 | |||||
chr19:15541865
|
C | CAA | 14 | a0001c0001t0001g0309a0001c0001t0002g0066a0001c0001t0002g0180others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.939+1165_939+1166d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15541865 | |||||
chr19:15541865
|
CA | C | 8 | a0001c0001t0001g0072a0001c0001t0002g0020a0001c0001t0003g0181others(5): Show | 8 | HG01167.hp1 HG01168.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.939+1166delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15541865 | |||||
chr19:15541877
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1160A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541877 | ||||||
chr19:15541878
|
A | G | 163 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0035others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.939+1161A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541878 | ||||||
chr19:15541883
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1166A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541883 | ||||||
chr19:15541884
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1167G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15541884 | ||||||
chr19:15542107
|
C | A | 1 | a0001c0001t0003g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.939+1390C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542107 | ||||||
chr19:15542148
|
A | G | 3 | a0001c0005t0002g0015a0001c0005t0004g0017a0001c0005t0004g0018 | 3 | HG02257.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.939+1431A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542148 | ||||||
chr19:15542187
|
C | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0230others(25): Show | 29 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.939+1470C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542187 | ||||||
chr19:15542201
|
C | A | 1 | a0001c0001t0002g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.939+1484C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542201 | ||||||
chr19:15542218
|
T | G | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.939+1501T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542218 | ||||||
chr19:15542337
|
G | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.939+1620G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542337 | ||||||
chr19:15542375
|
T | TA | 228 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0033others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.940-1586dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15542375 | |||||
chr19:15542389
|
T | C | 25 | a0001c0001t0002g0314a0001c0001t0002g0337a0001c0001t0004g0034others(22): Show | 26 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.940-1582T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542389 | ||||||
chr19:15542390
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.940-1581A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542390 | ||||||
chr19:15542397
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.940-1574C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542397 | ||||||
chr19:15542462
|
T | G | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.940-1509T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542462 | ||||||
chr19:15542503
|
C | G | 2 | a0002c0003t0004g0329a0002c0003t0004g0330 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.940-1468C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542503 | ||||||
chr19:15542523
|
A | G | 27 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0230others(24): Show | 28 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.940-1448A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542523 | ||||||
chr19:15542542
|
A | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(293): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.940-1429A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542542 | ||||||
chr19:15542599
|
G | A | 1 | a0001c0002t0002g0251 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.940-1372G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542599 | ||||||
chr19:15542715
|
CT | C | 5 | a0001c0001t0002g0013a0001c0001t0004g0010a0001c0001t0004g0012others(2): Show | 5 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.940-1255delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542715 | ||||||
chr19:15542746
|
C | CT | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.940-1225_940-1224i others(3): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542746 | ||||||
chr19:15542756
|
C | G | 1 | a0001c0001t0002g0024 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.940-1215C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542756 | ||||||
chr19:15542862
|
G | C | 1 | a0001c0001t0002g0275 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.940-1109G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542862 | ||||||
chr19:15542979
|
T | C | 3 | a0001c0001t0001g0204a0001c0001t0002g0067a0001c0001t0002g0137 | 3 | HG02056.hp1 NA18940.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.940-992T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15542979 | ||||||
chr19:15543022
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0003g0218 | 2 | HG03453.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.940-949C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543022 | ||||||
chr19:15543023
|
G | A | 7 | a0001c0001t0001g0376a0001c0001t0002g0380a0001c0001t0004g0143others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.940-948G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543023 | ||||||
chr19:15543069
|
C | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0335 | 2 | HG00741.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.940-902C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543069 | ||||||
chr19:15543070
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.940-901G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543070 | ||||||
chr19:15543091
|
A | G | 1 | a0001c0001t0004g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.940-880A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543091 | ||||||
chr19:15543161
|
G | A | 1 | a0001c0001t0002g0214 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.940-810G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543161 | ||||||
chr19:15543207
|
C | G | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.940-764C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543207 | ||||||
chr19:15543238
|
C | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0151a0001c0001t0001g0230others(13): Show | 17 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.940-733C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543238 | ||||||
chr19:15543248
|
G | A | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.940-723G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543248 | ||||||
chr19:15543306
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0228 | 2 | HG00323.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.940-665C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543306 | ||||||
chr19:15543394
|
G | A | 1 | a0001c0001t0002g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.940-577G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543394 | ||||||
chr19:15543415
|
C | T | 1 | a0001c0001t0002g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.940-556C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543415 | ||||||
chr19:15543466
|
A | G | 2 | a0001c0001t0004g0119a0001c0001t0004g0120 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.940-505A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543466 | ||||||
chr19:15543805
|
C | T | 1 | a0001c0001t0004g0242 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.940-166C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543805 | ||||||
chr19:15543820
|
G | A | 223 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0033others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.940-151G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543820 | ||||||
chr19:15543821
|
C | T | 1 | a0001c0005t0002g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.940-150C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | chr19 | 15543821 | ||||||
chr19:15543858
|
GA | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0078others(85): Show | 90 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.940-94delA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15543858 | |||||
chr19:15543858
|
GAA | G | 195 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0030others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.940-95_940-94delAA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 15543858 | |||||
chr19:15544325
|
G | A | 1 | a0004c0007t0004g0111 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1136+46G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544325 | ||||||
chr19:15544342
|
C | G | 25 | a0001c0001t0002g0314a0001c0001t0002g0337a0001c0001t0004g0034others(22): Show | 26 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1136+63C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544342 | ||||||
chr19:15544357
|
C | T | 296 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(293): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1136+78C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544357 | ||||||
chr19:15544394
|
T | G | 1 | a0001c0001t0001g0352 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1136+115T>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544394 | ||||||
chr19:15544474
|
G | A | 4 | a0001c0001t0001g0340a0001c0001t0001g0356a0001c0001t0001g0361others(1): Show | 4 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+195G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544474 | ||||||
chr19:15544499
|
A | G | 164 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0035others(161): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.1136+220A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544499 | ||||||
chr19:15544521
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1136+242C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544521 | ||||||
chr19:15544738
|
C | A | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1136+459C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544738 | ||||||
chr19:15544798
|
C | T | 297 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(294): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1136+519C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544798 | ||||||
chr19:15544846
|
A | T | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1136+567A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544846 | ||||||
chr19:15544899
|
A | G | 5 | a0001c0001t0002g0013a0001c0001t0004g0010a0001c0001t0004g0012others(2): Show | 5 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136+620A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544899 | ||||||
chr19:15544933
|
T | C | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1136+654T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544933 | ||||||
chr19:15544948
|
C | T | 35 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0052others(32): Show | 35 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1136+669C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544948 | ||||||
chr19:15544953
|
C | T | 1 | a0001c0002t0003g0248 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1136+674C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15544953 | ||||||
chr19:15545027
|
C | T | 292 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0030others(289): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1136+748C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545027 | ||||||
chr19:15545104
|
T | TA | 223 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0030others(220): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1136+837dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545104 | |||||
chr19:15545104
|
T | TAA | 10 | a0001c0001t0002g0020a0001c0001t0002g0066a0001c0001t0002g0180others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1136+836_1136+837d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545104 | |||||
chr19:15545108
|
A | AT | 31 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0052others(28): Show | 31 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1136+829_1136+830i others(3): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545108 | ||||||
chr19:15545114
|
A | AC | 8 | a0001c0001t0002g0337a0001c0001t0004g0034a0001c0001t0004g0141others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1136+835_1136+836i others(3): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545114 | ||||||
chr19:15545234
|
CAT | C | 5 | a0001c0001t0002g0003a0001c0001t0002g0252a0001c0001t0002g0262others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1136+958_1136+959d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545234 | |||||
chr19:15545327
|
A | G | 1 | a0008c0018t0002g0379 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1136+1048A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545327 | ||||||
chr19:15545328
|
G | C | 27 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0052others(24): Show | 27 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1136+1049G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545328 | ||||||
chr19:15545395
|
T | C | 347 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(344): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1136+1116T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545395 | ||||||
chr19:15545570
|
AC | A | 78 | a0001c0001t0001g0030a0001c0001t0001g0040a0001c0001t0001g0055others(75): Show | 79 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.1136+1294delC | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545570 | |||||
chr19:15545582
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1136+1303G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545582 | ||||||
chr19:15545590
|
G | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0075a0001c0001t0002g0155others(9): Show | 13 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1136+1311G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545590 | ||||||
chr19:15545648
|
C | CA | 47 | a0001c0001t0001g0005a0001c0001t0001g0092a0001c0001t0001g0151others(44): Show | 47 | HG00408.hp1 HG00558.hp2 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.1136+1392dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAA | 6 | a0001c0001t0002g0325a0001c0001t0003g0001a0001c0001t0003g0144others(3): Show | 7 | HG00639.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1136+1390_1136+139 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAAA | 21 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0056others(18): Show | 21 | HG00621.hp2 HG00642.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1136+1389_1136+139 others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAAAAA | 11 | a0001c0001t0001g0002a0001c0001t0002g0043a0001c0001t0002g0099others(8): Show | 12 | HG01070.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136+1387_1136+139 others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAAAAAA | 32 | a0001c0001t0001g0047a0001c0001t0002g0019a0001c0001t0002g0022others(29): Show | 32 | HG00558.hp1 HG00609.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1136+1386_1136+139 others(11): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAAAAAA others(1): Show |
16 | a0001c0001t0001g0191a0001c0001t0002g0028a0001c0001t0002g0031others(13): Show | 16 | HG00673.hp1 HG01123.hp2 HG01168.hp2 others(13): Show |
intron_variant | MODIFIER | c.1136+1385_1136+139 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0002g0370 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1136+1381_1136+139 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0372a0002c0003t0003g0004a0005c0006t0005g0009 | 4 | HG01123.hp1 HG02922.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+1380_1136+139 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAAAAAA others(7): Show |
5 | a0001c0001t0002g0075a0002c0003t0002g0006a0002c0003t0002g0007others(2): Show | 5 | HG02055.hp2 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+1379_1136+139 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545648
|
C | CAAAAAAA others(8): Show |
2 | a0005c0006t0005g0302a0006c0016t0005g0129 | 2 | HG01109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1136+1378_1136+139 others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545648 | |||||
chr19:15545659
|
AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0002g0021a0001c0001t0002g0244a0001c0002t0002g0251others(1): Show | 4 | HG02257.hp1 HG03239.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136+1385_1136+139 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545659 | |||||
chr19:15545661
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0002g0337 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1136+1387_1136+139 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545661 | |||||
chr19:15545667
|
A | AAAAAAGA others(4): Show |
1 | a0001c0001t0002g0068 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1136+1392_1136+139 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545667 | |||||
chr19:15545667
|
A | G | 6 | a0001c0001t0003g0218a0001c0001t0004g0231a0001c0002t0003g0008others(3): Show | 6 | HG02717.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1136+1388A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545667 | ||||||
chr19:15545672
|
G | A | 64 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0052others(61): Show | 66 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.1136+1393G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545672 | ||||||
chr19:15545677
|
G | A | 17 | a0001c0001t0001g0051a0001c0001t0001g0072a0001c0001t0001g0074others(14): Show | 17 | HG00408.hp2 HG00733.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1136+1398G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545677 | ||||||
chr19:15545678
|
A | T | 192 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0035others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1136+1399A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545678 | ||||||
chr19:15545679
|
AAAGAAAA others(6): Show |
A | 5 | a0001c0001t0003g0218a0001c0001t0004g0231a0001c0002t0003g0008others(2): Show | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1136+1408_1136+142 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545679 | |||||
chr19:15545683
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1136+1404A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545683 | ||||||
chr19:15545683
|
A | T | 45 | a0001c0001t0001g0033a0001c0001t0001g0052a0001c0001t0001g0056others(42): Show | 47 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1136+1404A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545683 | ||||||
chr19:15545688
|
A | T | 9 | a0001c0001t0001g0051a0001c0001t0001g0072a0001c0001t0001g0074others(6): Show | 9 | HG00733.hp1 HG01517.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1136+1409A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545688 | ||||||
chr19:15545689
|
AAAG | A | 204 | a0001c0001t0001g0026a0001c0001t0001g0030a0001c0001t0001g0035others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1136+1416_1136+141 others(7): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545689 | |||||
chr19:15545692
|
G | GAA | 116 | a0001c0001t0001g0002a0001c0001t0001g0033a0001c0001t0001g0047others(113): Show | 119 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.1136+1414_1136+141 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545692 | |||||
chr19:15545692
|
G | GAAAAGAA | 13 | a0001c0001t0001g0051a0001c0001t0001g0072a0001c0001t0001g0074others(10): Show | 13 | HG00733.hp1 HG01517.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1136+1415_1136+141 others(11): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545692 | |||||
chr19:15545692
|
G | GAAAAGAA others(5): Show |
3 | a0001c0001t0002g0069a0001c0001t0002g0073a0001c0001t0002g0312 | 3 | HG03041.hp2 HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1136+1415_1136+141 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15545692 | |||||
chr19:15545708
|
G | A | 4 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0253others(1): Show | 4 | HG00544.hp1 HG02132.hp2 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1136+1429G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545708 | ||||||
chr19:15545795
|
G | A | 21 | a0001c0001t0002g0013a0001c0001t0003g0301a0001c0001t0003g0303others(18): Show | 21 | HG02109.hp2 HG02258.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.1136+1516G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545795 | ||||||
chr19:15545802
|
G | A | 13 | a0001c0001t0002g0020a0001c0001t0002g0155a0001c0001t0002g0337others(10): Show | 13 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1136+1523G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545802 | ||||||
chr19:15545861
|
G | A | 5 | a0001c0004t0001g0106a0001c0004t0001g0108a0001c0004t0001g0110others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1136+1582G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545861 | ||||||
chr19:15545873
|
G | C | 3 | a0001c0002t0003g0008a0001c0004t0002g0173a0005c0006t0002g0327 | 3 | HG02717.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1136+1594G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545873 | ||||||
chr19:15545948
|
T | C | 1 | a0001c0001t0002g0031 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1136+1669T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15545948 | ||||||
chr19:15546039
|
A | C | 1 | a0001c0002t0003g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1136+1760A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546039 | ||||||
chr19:15546302
|
G | A | 65 | a0001c0001t0001g0309a0001c0001t0002g0019a0001c0001t0002g0022others(62): Show | 65 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1137-1806G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546302 | ||||||
chr19:15546601
|
C | T | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1137-1507C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546601 | ||||||
chr19:15546614
|
ACTAAT | A | 5 | a0005c0006t0002g0327a0005c0006t0005g0009a0005c0006t0005g0302others(2): Show | 5 | HG01109.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-1485_1137-148 others(9): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15546614 | |||||
chr19:15546891
|
G | T | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1137-1217G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546891 | ||||||
chr19:15546956
|
T | C | 2 | a0001c0001t0004g0184a0001c0001t0009g0011 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1137-1152T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546956 | ||||||
chr19:15546963
|
G | A | 324 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(321): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.1137-1145G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546963 | ||||||
chr19:15546992
|
T | C | 21 | a0001c0001t0001g0033a0001c0001t0001g0051a0001c0001t0001g0052others(18): Show | 21 | HG00642.hp1 HG00733.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1137-1116T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15546992 | ||||||
chr19:15547018
|
G | GT | 11 | a0001c0001t0003g0160a0001c0001t0003g0162a0001c0001t0003g0174others(8): Show | 12 | HG00733.hp2 HG01175.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.1137-1068dupT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTT | 32 | a0001c0001t0003g0023a0001c0001t0003g0303a0001c0001t0004g0010others(29): Show | 32 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1137-1069_1137-106 others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTT | 13 | a0001c0001t0002g0043a0001c0001t0002g0066a0001c0001t0002g0068others(10): Show | 13 | HG01070.hp1 HG02145.hp2 HG03579.hp1 others(10): Show |
intron_variant | MODIFIER | c.1137-1072_1137-106 others(9): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(1): Show |
72 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0033others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1137-1075_1137-106 others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(2): Show |
59 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0040others(56): Show | 60 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1137-1076_1137-106 others(13): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(3): Show |
13 | a0001c0001t0001g0056a0001c0001t0001g0182a0001c0001t0001g0200others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1137-1077_1137-106 others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0344a0001c0001t0001g0361a0002c0003t0001g0323 | 3 | HG00099.hp1 HG02280.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1137-1078_1137-106 others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0151a0001c0001t0012g0136 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1137-1079_1137-106 others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(6): Show |
14 | a0001c0001t0002g0038a0001c0001t0002g0041a0001c0001t0002g0049others(11): Show | 14 | HG00609.hp2 HG00735.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.1137-1080_1137-106 others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(7): Show |
30 | a0001c0001t0002g0013a0001c0001t0002g0019a0001c0001t0002g0022others(27): Show | 30 | HG00408.hp1 HG00558.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1137-1081_1137-106 others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(8): Show |
19 | a0001c0001t0002g0036a0001c0001t0002g0048a0001c0001t0002g0079others(16): Show | 19 | HG00673.hp1 HG01081.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.1137-1082_1137-106 others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(9): Show |
8 | a0001c0001t0002g0142a0001c0001t0002g0166a0001c0001t0002g0176others(5): Show | 8 | HG01358.hp2 HG02257.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-1083_1137-106 others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0005g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1137-1084_1137-106 others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(11): Show |
3 | a0001c0001t0002g0031a0001c0001t0002g0380a0006c0017t0002g0368 | 3 | HG02809.hp2 HG03453.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1137-1085_1137-106 others(22): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(12): Show |
3 | a0001c0001t0002g0101a0002c0003t0005g0328a0006c0016t0005g0129 | 3 | HG01109.hp1 HG03130.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1137-1086_1137-106 others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(13): Show |
2 | a0002c0003t0005g0315a0005c0006t0005g0302 | 2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1137-1087_1137-106 others(24): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(14): Show |
1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1137-1088_1137-106 others(25): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(16): Show |
2 | a0001c0005t0004g0018a0004c0007t0004g0111 | 2 | HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1137-1068_1137-106 others(27): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(17): Show |
1 | a0001c0005t0004g0017 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1137-1068_1137-106 others(28): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0004g0231 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1137-1068_1137-106 others(29): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
G | GTTTTTTT others(23): Show |
1 | a0009c0015t0004g0221 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1137-1068_1137-106 others(34): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547018
|
GT | G | 20 | a0001c0001t0002g0003a0001c0001t0002g0021a0001c0001t0002g0032others(17): Show | 21 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1137-1068delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547018 | |||||
chr19:15547074
|
A | C | 1 | a0001c0001t0012g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1137-1034A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547074 | ||||||
chr19:15547078
|
T | C | 1 | a0001c0001t0009g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1137-1030T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547078 | ||||||
chr19:15547109
|
C | T | 23 | a0001c0001t0002g0003a0001c0001t0002g0021a0001c0001t0002g0032others(20): Show | 24 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1137-999C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547109 | ||||||
chr19:15547117
|
G | A | 3 | a0001c0001t0002g0068a0001c0001t0002g0155a0010c0010t0002g0202 | 3 | HG01361.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1137-991G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547117 | ||||||
chr19:15547123
|
A | C | 15 | a0001c0001t0002g0043a0001c0001t0002g0066a0001c0001t0002g0164others(12): Show | 15 | HG01070.hp1 HG02145.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137-985A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547123 | ||||||
chr19:15547228
|
T | C | 23 | a0001c0001t0002g0003a0001c0001t0002g0021a0001c0001t0002g0032others(20): Show | 24 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1137-880T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547228 | ||||||
chr19:15547266
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1137-842C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547266 | ||||||
chr19:15547282
|
T | C | 11 | a0001c0001t0004g0184a0001c0001t0005g0241a0001c0001t0009g0011others(8): Show | 11 | HG01109.hp1 HG02258.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1137-826T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547282 | ||||||
chr19:15547411
|
C | A | 1 | a0002c0003t0002g0362 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-697C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547411 | ||||||
chr19:15547560
|
C | A | 2 | a0001c0001t0004g0184a0001c0001t0009g0011 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1137-548C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547560 | ||||||
chr19:15547588
|
C | G | 1 | a0001c0001t0002g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1137-520C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547588 | ||||||
chr19:15547639
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1137-469A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547639 | ||||||
chr19:15547648
|
C | A | 1 | a0001c0001t0001g0147 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1137-460C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547648 | ||||||
chr19:15547771
|
C | T | 1 | a0001c0004t0004g0107 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1137-337C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547771 | ||||||
chr19:15547777
|
G | T | 1 | a0001c0001t0012g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1137-331G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547777 | ||||||
chr19:15547803
|
C | G | 1 | a0001c0001t0009g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1137-305C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547803 | ||||||
chr19:15547817
|
G | A | 1 | a0004c0007t0001g0285 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1137-291G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547817 | ||||||
chr19:15547921
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1137-187T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547921 | ||||||
chr19:15547968
|
T | TGA | 3 | a0001c0001t0002g0022a0001c0001t0002g0239a0001c0001t0005g0241 | 3 | HG00609.hp2 HG04184.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1137-114_1137-113d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547968 | |||||
chr19:15547968
|
TGA | T | 9 | a0001c0001t0001g0367a0001c0001t0003g0171a0001c0001t0003g0181others(6): Show | 10 | HG00738.hp1 HG01168.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-114_1137-113d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547968 | |||||
chr19:15547982
|
AGAGAGAG others(7): Show |
A | 1 | a0001c0001t0008g0286 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1137-118_1137-105d others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547982 | |||||
chr19:15547984
|
AGAGAGAG others(5): Show |
A | 1 | a0001c0001t0001g0035 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1137-116_1137-105d others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547984 | |||||
chr19:15547986
|
AGAGAGAG others(3): Show |
A | 36 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0088others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.1137-114_1137-105d others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547986 | |||||
chr19:15547988
|
AGAGAGAG others(1): Show |
A | 18 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0001g0203others(15): Show | 18 | HG00544.hp1 HG00621.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1137-112_1137-105d others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547988 | |||||
chr19:15547988
|
AGAGAGAG others(9): Show |
A | 5 | a0001c0001t0004g0231a0001c0001t0007g0322a0001c0004t0007g0060others(2): Show | 5 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-118_1137-103d others(18): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547988 | |||||
chr19:15547988
|
AGAGAGAG others(11): Show |
A | 4 | a0001c0005t0004g0017a0001c0005t0004g0018a0004c0007t0004g0111others(1): Show | 4 | HG02572.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-118_1137-101d others(20): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547988 | |||||
chr19:15547988
|
AGAGAGAG others(17): Show |
A | 2 | a0001c0001t0002g0146a0001c0002t0002g0126 | 2 | HG01243.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1137-118_1137-95de others(25): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547988 | |||||
chr19:15547990
|
AGAGAGG | A | 33 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0206others(30): Show | 33 | HG00558.hp2 HG00735.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1137-112_1137-107d others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547990 | |||||
chr19:15547990
|
AGAGAGGG others(7): Show |
A | 1 | a0001c0001t0001g0081 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1137-116_1137-103d others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547990 | |||||
chr19:15547992
|
A | AGG | 2 | a0001c0001t0003g0001a0001c0001t0003g0023 | 3 | HG00621.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1137-115_1137-114i others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGG | A | 20 | a0001c0001t0001g0094a0001c0001t0001g0376a0001c0001t0002g0019others(17): Show | 20 | HG00558.hp1 HG01081.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1137-112_1137-109d others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGGGAG others(5): Show |
A | 49 | a0001c0001t0001g0030a0001c0001t0001g0051a0001c0001t0001g0052others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1137-114_1137-103d others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGGGAG others(7): Show |
A | 9 | a0001c0001t0001g0026a0001c0001t0001g0078a0001c0001t0001g0151others(6): Show | 9 | HG00741.hp2 HG01123.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-114_1137-101d others(16): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGGGAG others(9): Show |
A | 9 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0072others(6): Show | 10 | HG00642.hp1 HG01109.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1137-114_1137-99de others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGGGAG others(11): Show |
A | 2 | a0001c0001t0002g0262a0001c0001t0002g0345 | 2 | HG01169.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1137-114_1137-97de others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGGGAG others(13): Show |
A | 13 | a0001c0001t0002g0003a0001c0001t0002g0061a0001c0001t0002g0117others(10): Show | 14 | HG01069.hp1 HG01071.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1137-114_1137-95de others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGGGAG others(15): Show |
A | 2 | a0001c0001t0002g0032a0001c0001t0002g0246 | 2 | HG02735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1137-114_1137-93de others(23): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGGGAG others(17): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1137-114_1137-91de others(25): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547992
|
AGAGGGAG others(21): Show |
A | 1 | a0005c0006t0005g0009 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1137-114_1137-87de others(29): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547992 | |||||
chr19:15547994
|
A | G | 3 | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0354 | 3 | HG00140.hp2 HG00639.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1137-114A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547994 | ||||||
chr19:15547994
|
AGG | A | 5 | a0001c0001t0002g0103a0001c0001t0002g0137a0001c0001t0002g0273others(2): Show | 5 | HG01358.hp2 HG01515.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-112_1137-111d others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | |||||
chr19:15547994
|
AGGGAGAG others(3): Show |
A | 10 | a0001c0001t0001g0047a0001c0001t0001g0182a0001c0001t0001g0193others(7): Show | 10 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-112_1137-103d others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | |||||
chr19:15547994
|
AGGGAGAG others(5): Show |
A | 16 | a0001c0001t0001g0033a0001c0001t0001g0040a0001c0001t0001g0113others(13): Show | 16 | HG00735.hp2 HG01074.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1137-112_1137-101d others(14): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | |||||
chr19:15547994
|
AGGGAGAG others(7): Show |
A | 24 | a0001c0001t0002g0013a0001c0001t0004g0010a0001c0001t0004g0012others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1137-112_1137-99de others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | |||||
chr19:15547994
|
AGGGAGAG others(9): Show |
A | 15 | a0001c0001t0002g0024a0001c0001t0002g0127a0001c0001t0002g0153others(12): Show | 15 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1137-112_1137-97de others(17): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | |||||
chr19:15547994
|
AGGGAGAG others(11): Show |
A | 1 | a0001c0001t0002g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1137-112_1137-95de others(19): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | |||||
chr19:15547994
|
AGGGAGAG others(13): Show |
A | 4 | a0001c0001t0002g0042a0001c0001t0002g0064a0001c0001t0002g0290others(1): Show | 4 | HG01952.hp1 HG02735.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-112_1137-93de others(21): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547994 | |||||
chr19:15547996
|
G | A | 44 | a0001c0001t0002g0020a0001c0001t0002g0043a0001c0001t0002g0063others(41): Show | 45 | HG00140.hp2 HG00621.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1137-112G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547996 | ||||||
chr19:15547996
|
G | T | 3 | a0001c0001t0001g0367a0001c0001t0002g0022a0001c0001t0002g0239 | 3 | HG00609.hp2 HG04184.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1137-112G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547996 | ||||||
chr19:15547998
|
A | T | 8 | a0001c0001t0001g0094a0001c0001t0001g0367a0001c0001t0001g0376others(5): Show | 8 | HG00609.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-110A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15547998 | ||||||
chr19:15547998
|
AGAGAGTG others(7): Show |
A | 1 | a0001c0001t0004g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1137-108_1137-95de others(15): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15547998 | |||||
chr19:15548000
|
A | T | 16 | a0001c0001t0001g0094a0001c0001t0001g0206a0001c0001t0001g0245others(13): Show | 17 | HG00558.hp2 HG00609.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.1137-108A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548000 | ||||||
chr19:15548002
|
A | AGAGTGTG others(3): Show |
1 | a0001c0002t0002g0311 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1137-105_1137-104i others(12): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548002
|
A | AGT | 17 | a0001c0001t0003g0044a0001c0001t0003g0054a0001c0001t0003g0059others(14): Show | 17 | HG01081.hp2 HG01109.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1137-59_1137-58dup others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548002
|
A | AGTGT | 8 | a0001c0001t0003g0070a0001c0001t0003g0218a0001c0001t0003g0296others(5): Show | 8 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-61_1137-58dup others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548002
|
A | AGTGTGTG others(3): Show |
3 | a0001c0001t0002g0068a0001c0001t0003g0358a0002c0003t0003g0363 | 3 | HG01167.hp1 HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1137-67_1137-58dup others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548002
|
A | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0056a0001c0001t0001g0077others(38): Show | 42 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1137-106A>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548002 | ||||||
chr19:15548002
|
AGT | A | 8 | a0001c0001t0003g0152a0001c0001t0003g0174a0001c0001t0003g0188others(5): Show | 9 | HG01257.hp1 HG01928.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-59_1137-58del others(2): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548002
|
AGTGT | A | 3 | a0001c0001t0002g0192a0001c0001t0002g0359a0002c0003t0002g0362 | 3 | HG02818.hp2 HG03927.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1137-61_1137-58del others(4): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548002
|
AGTGTGT | A | 8 | a0001c0001t0002g0043a0001c0001t0002g0217a0001c0001t0002g0224others(5): Show | 8 | HG01070.hp1 HG03225.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-63_1137-58del others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548002
|
AGTGTGTG others(1): Show |
A | 5 | a0001c0001t0002g0066a0001c0001t0002g0180a0001c0001t0002g0232others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1137-65_1137-58del others(8): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548002
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0003g0160 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1137-67_1137-58del others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548002 | |||||
chr19:15548004
|
T | A | 20 | a0001c0001t0002g0031a0001c0001t0002g0036a0001c0001t0002g0039others(17): Show | 20 | HG01358.hp2 HG01515.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1137-104T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548004 | ||||||
chr19:15548006
|
T | A | 10 | a0001c0001t0002g0103a0001c0001t0002g0104a0001c0001t0002g0142others(7): Show | 10 | HG00408.hp1 HG01358.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1137-102T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548006 | ||||||
chr19:15548008
|
T | A | 8 | a0001c0001t0001g0134a0001c0001t0002g0103a0001c0001t0002g0192others(5): Show | 8 | HG01358.hp2 HG01515.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1137-100T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548008 | ||||||
chr19:15548010
|
T | A | 11 | a0001c0001t0002g0013a0001c0001t0002g0043a0001c0001t0002g0217others(8): Show | 11 | HG01070.hp1 HG02145.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1137-98T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548010 | ||||||
chr19:15548012
|
T | A | 15 | a0001c0001t0002g0043a0001c0001t0002g0127a0001c0001t0002g0153others(12): Show | 15 | HG01070.hp1 HG01891.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.1137-96T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548012 | ||||||
chr19:15548016
|
T | A | 1 | a0001c0001t0002g0380 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1137-92T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548016 | ||||||
chr19:15548041
|
G | T | 2 | a0001c0001t0004g0184a0001c0001t0009g0011 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1137-67G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548041 | ||||||
chr19:15548049
|
GT | G | 7 | a0001c0001t0001g0078a0001c0001t0001g0156a0001c0001t0001g0259others(4): Show | 7 | HG00544.hp1 HG01123.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1137-55delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 15548049 | |||||
chr19:15548081
|
C | G | 1 | a0008c0018t0002g0379 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1137-27C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 10/13 | chr19 | 15548081 | ||||||
chr19:15548257
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1270+16C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548257 | ||||||
chr19:15548372
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0191a0001c0001t0001g0207others(5): Show | 9 | HG02015.hp2 HG02071.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.1270+131T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548372 | ||||||
chr19:15548382
|
G | A | 3 | a0001c0001t0002g0068a0001c0001t0002g0155a0010c0010t0002g0202 | 3 | HG01361.hp1 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1270+141G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548382 | ||||||
chr19:15548384
|
G | T | 2 | a0001c0001t0004g0184a0001c0001t0009g0011 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1270+143G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548384 | ||||||
chr19:15548405
|
G | C | 5 | a0001c0001t0002g0050a0001c0001t0002g0079a0001c0001t0002g0080others(2): Show | 5 | HG00408.hp2 HG00673.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1270+164G>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548405 | ||||||
chr19:15548427
|
G | T | 11 | a0001c0001t0001g0051a0001c0001t0001g0056a0001c0001t0001g0077others(8): Show | 11 | HG02683.hp1 HG03704.hp2 HG03831.hp2 others(8): Show |
intron_variant | MODIFIER | c.1270+186G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548427 | ||||||
chr19:15548643
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1270+402A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548643 | ||||||
chr19:15548660
|
A | G | 3 | a0001c0001t0005g0241a0002c0003t0005g0315a0002c0003t0005g0328 | 3 | HG02965.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1270+419A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548660 | ||||||
chr19:15548766
|
G | A | 2 | a0001c0001t0004g0184a0001c0001t0009g0011 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1271-372G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548766 | ||||||
chr19:15548949
|
G | A | 2 | a0001c0001t0004g0184a0001c0001t0009g0011 | 2 | HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1271-189G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 11/13 | chr19 | 15548949 | ||||||
chr19:15549219
|
C | G | 5 | a0001c0001t0004g0184a0001c0001t0005g0241a0001c0001t0009g0011others(2): Show | 5 | HG02559.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1335+17C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549219 | ||||||
chr19:15549286
|
G | T | 1 | a0001c0001t0012g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1335+84G>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549286 | ||||||
chr19:15549488
|
AT | A | 9 | a0001c0001t0002g0013a0001c0001t0002g0024a0001c0001t0002g0127others(6): Show | 9 | HG01891.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1335+287delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549488 | ||||||
chr19:15549563
|
C | A | 1 | a0001c0001t0001g0372 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1335+361C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549563 | ||||||
chr19:15549592
|
C | T | 1 | a0001c0001t0004g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1335+390C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549592 | ||||||
chr19:15549773
|
C | T | 1 | a0001c0001t0009g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1335+571C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549773 | ||||||
chr19:15549804
|
T | TA | 191 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1335+615dupA | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 15549804 | |||||
chr19:15549815
|
A | C | 1 | a0002c0003t0002g0362 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1335+613A>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549815 | ||||||
chr19:15549824
|
C | A | 1 | a0002c0003t0002g0362 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1335+622C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549824 | ||||||
chr19:15549992
|
G | A | 1 | a0001c0001t0004g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1336-682G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15549992 | ||||||
chr19:15550034
|
T | A | 1 | a0002c0003t0001g0377 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1336-640T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550034 | ||||||
chr19:15550134
|
T | C | 3 | a0001c0001t0005g0241a0002c0003t0005g0315a0002c0003t0005g0328 | 3 | HG02965.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1336-540T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550134 | ||||||
chr19:15550247
|
C | A | 2 | a0001c0001t0002g0020a0001c0002t0002g0311 | 2 | HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1336-427C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550247 | ||||||
chr19:15550285
|
TAACA | T | 5 | a0001c0001t0001g0376a0001c0004t0001g0106a0001c0004t0001g0108others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-370_1336-367d others(6): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 15550285 | |||||
chr19:15550285
|
TAACAAAC others(1): Show |
T | 3 | a0001c0001t0004g0184a0001c0001t0009g0011a0001c0001t0012g0136 | 3 | HG02258.hp2 HG02559.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1336-374_1336-367d others(10): Show |
CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr19 | 15550285 | |||||
chr19:15550322
|
C | A | 3 | a0001c0001t0005g0241a0002c0003t0005g0315a0002c0003t0005g0328 | 3 | HG02965.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1336-352C>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550322 | ||||||
chr19:15550327
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1336-347A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550327 | ||||||
chr19:15550341
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1336-333G>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550341 | ||||||
chr19:15550368
|
T | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(186): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1336-306T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550368 | ||||||
chr19:15550485
|
C | T | 1 | a0001c0001t0004g0184 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1336-189C>T | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550485 | ||||||
chr19:15550497
|
T | A | 4 | a0001c0005t0004g0017a0001c0005t0004g0018a0004c0007t0004g0111others(1): Show | 4 | HG02572.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-177T>A | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550497 | ||||||
chr19:15550572
|
CT | C | 51 | a0001c0001t0002g0019a0001c0001t0002g0022a0001c0001t0002g0028others(48): Show | 51 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.1336-101delT | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 12/13 | chr19 | 15550572 | ||||||
chr19:15550893
|
A | G | 1 | a0008c0018t0002g0379 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1418+137A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 13/13 | chr19 | 15550893 | ||||||
chr19:15551065
|
A | G | 231 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(228): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1419-229A>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 13/13 | chr19 | 15551065 | ||||||
chr19:15551107
|
T | C | 1 | a0001c0001t0002g0169 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1419-187T>C | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 13/13 | chr19 | 15551107 | ||||||
chr19:15551235
|
C | G | 2 | a0001c0001t0009g0011a0001c0001t0012g0136 | 2 | HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1419-59C>G | CYP4F22 | ENSG00000171954.13 | transcript | ENST00000269703.8 | protein_coding | 13/13 | chr19 | 15551235 |