geneid | 339761 |
---|---|
ensemblid | ENSG00000186684.14 |
hgncid | 33480 |
symbol | CYP27C1 |
name | cytochrome P450 family 27 subfamily C member 1 |
refseq_nuc | NM_001367502.1 |
refseq_prot | NP_001354431.1 |
ensembl_nuc | ENST00000664447.2 |
ensembl_prot | ENSP00000499243.1 |
mane_status | MANE Select |
chr | chr2 |
start | 127183832 |
end | 127220299 |
strand | - |
ver | v1.2 |
region | chr2:127183832-127220299 |
region5000 | chr2:127178832-127225299 |
regionname0 | CYP27C1_chr2_127183832_127220299 |
regionname5000 | CYP27C1_chr2_127178832_127225299 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 537 | 322 | 73 | 68 | 129 | 10 | 41 | 91 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002 | 0/0 | 537 | 15 | 14 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0003 | 0/0 | 537 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0004 | 0/0 | 537 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0005 | 0/0 | 537 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0006 | 0/0 | 537 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0007 | 0/1 | 537 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0008 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0009 | 0/0 | 537 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1614 | 240 | 41 | 52 | 112 | 7 | 27 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0002 | 0/0 | 1614 | 75 | 31 | 10 | 17 | 3 | 14 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0003 | 0/0 | 1614 | 8 | 7 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0004 | 0/0 | 1614 | 7 | 7 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0005 | 0/0 | 1614 | 5 | 0 | 5 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0006 | 0/0 | 1614 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0007 | 0/0 | 1614 | 3 | 2 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0008 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0009 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0010 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0011 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0012 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0013 | 0/1 | 1614 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0014 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0015 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
c0016 | 0/0 | 1614 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3470 | 111 | 16 | 28 | 52 | 3 | 11 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0002 | 0/0 | 3474 | 83 | 3 | 25 | 40 | 4 | 11 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0003 | 0/0 | 3475 | 21 | 12 | 5 | 4 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0004 | 0/0 | 3470 | 15 | 0 | 2 | 3 | 3 | 7 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0005 | 0/0 | 3480 | 12 | 0 | 1 | 9 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0006 | 0/0 | 3465 | 12 | 6 | 0 | 4 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0007 | 0/0 | 3465 | 11 | 6 | 3 | 0 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0008 | 0/0 | 3465 | 7 | 7 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0009 | 0/0 | 3465 | 6 | 6 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0010 | 0/0 | 3465 | 5 | 5 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0011 | 0/0 | 3470 | 5 | 4 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0012 | 0/0 | 3479 | 4 | 2 | 0 | 1 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0013 | 1/0 | 3469 | 4 | 0 | 1 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0014 | 0/0 | 3475 | 3 | 0 | 0 | 2 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0015 | 0/0 | 3470 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0016 | 0/0 | 3465 | 3 | 2 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0017 | 0/0 | 3444 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0018 | 0/0 | 3475 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0019 | 0/0 | 3472 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0020 | 0/0 | 3465 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0021 | 0/0 | 3470 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0022 | 0/0 | 3470 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0023 | 0/0 | 3470 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0024 | 0/0 | 3474 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0025 | 0/0 | 3474 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0026 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0027 | 0/0 | 3470 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0028 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0029 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0030 | 0/0 | 3480 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0031 | 0/0 | 3475 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0032 | 0/0 | 3470 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0033 | 0/0 | 3470 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0034 | 0/0 | 3470 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0035 | 0/0 | 3470 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0036 | 0/0 | 3470 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0037 | 0/0 | 3470 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0038 | 0/0 | 3470 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0039 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0040 | 0/0 | 3465 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0041 | 0/0 | 3467 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0042 | 0/0 | 3465 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0043 | 0/0 | 3474 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0044 | 0/0 | 3479 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0045 | 0/0 | 3474 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0046 | 0/0 | 3474 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0047 | 0/0 | 3474 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0048 | 0/0 | 3474 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0049 | 0/0 | 3464 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
t0050 | 0/0 | 3474 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1614 | 240 | 41 | 52 | 112 | 7 | 27 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002 | 0/0 | 1614 | 75 | 31 | 10 | 17 | 3 | 14 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0005 | 0/0 | 1614 | 5 | 0 | 5 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0012 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0014 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002c0003 | 0/0 | 1614 | 8 | 7 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002c0004 | 0/0 | 1614 | 7 | 7 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0003c0006 | 0/0 | 1614 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0003c0008 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0003c0010 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0004c0007 | 0/0 | 1614 | 3 | 2 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0005c0009 | 0/0 | 1614 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0006c0011 | 0/0 | 1614 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0007c0013 | 0/1 | 1614 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0008c0015 | 0/0 | 1614 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0009c0016 | 0/0 | 1614 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5083 | 108 | 15 | 27 | 52 | 3 | 11 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0002 | 0/0 | 5087 | 75 | 3 | 19 | 39 | 4 | 10 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0003 | 0/0 | 5088 | 18 | 10 | 4 | 4 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0005 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0006 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0008 | 0/0 | 5078 | 4 | 4 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0010 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0012 | 0/0 | 5092 | 4 | 2 | 0 | 1 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0013 | 1/0 | 5082 | 4 | 0 | 1 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0015 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0021 | 0/0 | 5083 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0023 | 0/0 | 5083 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0024 | 0/0 | 5087 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0025 | 0/0 | 5087 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0030 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0033 | 0/0 | 5083 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0034 | 0/0 | 5083 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0035 | 0/0 | 5083 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0036 | 0/0 | 5083 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0038 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0040 | 0/0 | 5078 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0043 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0044 | 0/0 | 5092 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0045 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0046 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0047 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0048 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0049 | 0/0 | 5077 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0001t0050 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0001 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0004 | 0/0 | 5083 | 15 | 0 | 2 | 3 | 3 | 7 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0005 | 0/0 | 5093 | 11 | 0 | 1 | 8 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0006 | 0/0 | 5078 | 8 | 2 | 0 | 4 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0007 | 0/0 | 5078 | 11 | 6 | 3 | 0 | 0 | 2 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0009 | 0/0 | 5078 | 6 | 6 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0011 | 0/0 | 5083 | 5 | 4 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0014 | 0/0 | 5088 | 3 | 0 | 0 | 2 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0015 | 0/0 | 5083 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0016 | 0/0 | 5078 | 3 | 2 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0018 | 0/0 | 5088 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0022 | 0/0 | 5083 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0031 | 0/0 | 5088 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0032 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0037 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0039 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0002t0042 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0005t0002 | 0/0 | 5087 | 5 | 0 | 5 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0012t0001 | 0/0 | 5083 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0001c0014t0008 | 0/0 | 5078 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002c0003t0003 | 0/0 | 5088 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002c0003t0006 | 0/0 | 5078 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002c0003t0010 | 0/0 | 5078 | 4 | 4 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002c0004t0019 | 0/0 | 5085 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002c0004t0020 | 0/0 | 5078 | 3 | 3 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0002c0004t0041 | 0/0 | 5080 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0003c0006t0017 | 0/0 | 5057 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0003c0006t0028 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0003c0008t0008 | 0/0 | 5078 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0003c0010t0029 | 0/0 | 5088 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0004c0007t0002 | 0/0 | 5087 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0004c0007t0026 | 0/0 | 5088 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0004c0007t0027 | 0/0 | 5083 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0005c0009t0003 | 0/0 | 5088 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0006c0011t0002 | 0/0 | 5087 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0007c0013t0001 | 0/1 | 5083 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0008c0015t0017 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
a0009c0016t0002 | 0/0 | 5087 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | copy fasta | chr2 | 127178832 | 127225299 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0008g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0008g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0010g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0012g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0012g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0012g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0013g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0013g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0013g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0013g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0015g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0021g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0021g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0023g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0024g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0024g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0025g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0025g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0030g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0033g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0034g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0035g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0036g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0038g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0040g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0043g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0044g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0045g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0046g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0047g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0048g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0049g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0001t0050g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0005g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0006g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0006g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0011g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0011g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0011g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0014g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0014g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0014g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0015g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0015g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0016g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0016g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0016g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0018g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0018g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0018g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0022g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0031g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0032g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0037g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0039g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0002t0042g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0005t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0005t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0005t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0005t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0005t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0012t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0001c0014t0008g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0003t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0003t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0003t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0003t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0003t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0003t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0003t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0003t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0004t0019g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0004t0019g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0004t0019g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0004t0020g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0004t0020g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0004t0020g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0002c0004t0041g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0003c0006t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0003c0006t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0003c0006t0028g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0003c0008t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0003c0008t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0003c0010t0029g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0004c0007t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0004c0007t0026g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0004c0007t0027g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0005c0009t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0006c0011t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0007c0013t0001g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0008c0015t0017g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
a0009c0016t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0002 | g0145 | EUR | FIN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0163 | EUR | FIN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00423 | hp1 | a0001 | c0001 | t0047 | g0038 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00609 | hp1 | a0001 | c0002 | t0004 | g0070 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00642 | hp2 | a0001 | c0005 | t0002 | g0267 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01069 | hp1 | a0001 | c0005 | t0002 | g0120 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01069 | hp2 | a0001 | c0001 | t0040 | g0226 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01071 | hp1 | a0001 | c0005 | t0002 | g0108 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0316 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01168 | hp1 | a0006 | c0011 | t0002 | g0013 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01168 | hp2 | a0001 | c0002 | t0007 | g0059 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01169 | hp1 | a0001 | c0002 | t0007 | g0083 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01175 | hp2 | a0001 | c0002 | t0016 | g0331 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01192 | hp2 | a0001 | c0002 | t0004 | g0088 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01243 | hp1 | a0002 | c0003 | t0003 | g0024 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01243 | hp2 | a0001 | c0002 | t0011 | g0047 | AMR | PUR | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01256 | hp1 | a0001 | c0002 | t0022 | g0002 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01258 | hp1 | a0001 | c0002 | t0022 | g0002 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01346 | hp2 | a0001 | c0005 | t0002 | g0031 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01433 | hp1 | a0001 | c0012 | t0001 | g0090 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01433 | hp2 | a0001 | c0005 | t0002 | g0277 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01515 | hp1 | a0001 | c0002 | t0004 | g0072 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0112 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01517 | hp1 | a0001 | c0002 | t0004 | g0052 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01884 | hp1 | a0001 | c0002 | t0009 | g0064 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0325 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01891 | hp1 | a0001 | c0002 | t0009 | g0057 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01891 | hp2 | a0001 | c0002 | t0007 | g0335 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01943 | hp1 | a0001 | c0001 | t0013 | g0060 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01981 | hp1 | a0001 | c0002 | t0004 | g0033 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0318 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02015 | hp1 | a0001 | c0001 | t0023 | g0209 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02015 | hp2 | a0001 | c0002 | t0006 | g0093 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02027 | hp2 | a0001 | c0002 | t0005 | g0039 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02055 | hp2 | a0001 | c0002 | t0011 | g0050 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02056 | hp1 | a0001 | c0001 | t0036 | g0201 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02056 | hp2 | a0001 | c0001 | t0024 | g0152 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02071 | hp2 | a0001 | c0002 | t0004 | g0087 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02074 | hp2 | a0001 | c0002 | t0005 | g0056 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02132 | hp2 | a0001 | c0001 | t0043 | g0162 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0190 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02145 | hp2 | a0002 | c0003 | t0010 | g0019 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0268 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | CDX | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | CDX | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CDX | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | CDX | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02257 | hp1 | a0001 | c0002 | t0007 | g0334 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02257 | hp2 | a0001 | c0002 | t0016 | g0332 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02258 | hp2 | a0001 | c0002 | t0015 | g0329 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0319 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0091 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02280 | hp2 | a0002 | c0003 | t0010 | g0017 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02293 | hp1 | a0001 | c0002 | t0007 | g0085 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02615 | hp1 | a0002 | c0004 | t0019 | g0014 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02615 | hp2 | a0001 | c0002 | t0018 | g0194 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02622 | hp2 | a0001 | c0002 | t0039 | g0048 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02630 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02630 | hp2 | a0002 | c0004 | t0041 | g0025 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02647 | hp1 | a0001 | c0002 | t0006 | g0042 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02647 | hp2 | a0003 | c0006 | t0028 | g0009 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02683 | hp1 | a0001 | c0002 | t0014 | g0074 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02683 | hp2 | a0001 | c0002 | t0004 | g0053 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0186 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02723 | hp2 | a0001 | c0002 | t0007 | g0337 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02738 | hp1 | a0001 | c0002 | t0004 | g0100 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02738 | hp2 | a0009 | c0016 | t0002 | g0345 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02809 | hp1 | a0001 | c0002 | t0011 | g0049 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02809 | hp2 | a0001 | c0002 | t0009 | g0081 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02818 | hp1 | a0002 | c0004 | t0019 | g0016 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02818 | hp2 | a0001 | c0002 | t0018 | g0223 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02886 | hp1 | a0001 | c0002 | t0007 | g0336 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02896 | hp1 | a0003 | c0006 | t0017 | g0010 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02896 | hp2 | a0005 | c0009 | t0003 | g0005 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02897 | hp1 | a0001 | c0002 | t0009 | g0086 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02897 | hp2 | a0005 | c0009 | t0003 | g0005 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02922 | hp1 | a0001 | c0001 | t0038 | g0339 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0326 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02965 | hp1 | a0002 | c0003 | t0006 | g0027 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02970 | hp1 | a0001 | c0002 | t0011 | g0063 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02976 | hp2 | a0001 | c0002 | t0009 | g0035 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03017 | hp1 | a0001 | c0002 | t0004 | g0068 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03041 | hp1 | a0001 | c0014 | t0008 | g0343 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03041 | hp2 | a0002 | c0004 | t0020 | g0022 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03098 | hp1 | a0003 | c0008 | t0008 | g0008 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03098 | hp2 | a0001 | c0001 | t0021 | g0321 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03130 | hp1 | a0004 | c0007 | t0027 | g0095 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03139 | hp1 | a0001 | c0001 | t0030 | g0217 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03139 | hp2 | a0002 | c0003 | t0006 | g0026 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03195 | hp2 | a0001 | c0002 | t0007 | g0094 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03209 | hp1 | a0002 | c0004 | t0019 | g0015 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03209 | hp2 | a0001 | c0002 | t0016 | g0333 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03225 | hp1 | a0002 | c0004 | t0020 | g0020 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03225 | hp2 | a0003 | c0008 | t0008 | g0007 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03239 | hp1 | a0001 | c0002 | t0007 | g0082 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03239 | hp2 | a0001 | c0002 | t0006 | g0089 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03453 | hp1 | a0001 | c0002 | t0018 | g0179 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03453 | hp2 | a0001 | c0002 | t0007 | g0327 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03486 | hp2 | a0002 | c0003 | t0010 | g0018 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03516 | hp1 | a0001 | c0002 | t0031 | g0065 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03516 | hp2 | a0001 | c0002 | t0015 | g0342 | AFR | ESN | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03540 | hp1 | a0001 | c0002 | t0011 | g0062 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03540 | hp2 | a0003 | c0010 | t0029 | g0011 | AFR | GWD | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03579 | hp1 | a0001 | c0002 | t0037 | g0037 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03579 | hp2 | a0002 | c0004 | t0020 | g0021 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03669 | hp1 | a0001 | c0001 | t0012 | g0140 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03669 | hp2 | a0001 | c0002 | t0005 | g0041 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03710 | hp1 | a0001 | c0002 | t0004 | g0069 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03710 | hp2 | a0001 | c0001 | t0049 | g0128 | SAS | PJL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03834 | hp2 | a0001 | c0002 | t0006 | g0075 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03927 | hp1 | a0001 | c0002 | t0004 | g0077 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03927 | hp2 | a0001 | c0001 | t0034 | g0308 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03942 | hp2 | a0001 | c0001 | t0045 | g0107 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04115 | hp1 | a0001 | c0001 | t0044 | g0177 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04199 | hp1 | a0001 | c0001 | t0048 | g0125 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04199 | hp2 | a0001 | c0002 | t0004 | g0040 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0151 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04228 | hp1 | a0001 | c0002 | t0005 | g0076 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0157 | SAS | STU | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | CHB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | CHB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18906 | hp1 | a0001 | c0002 | t0042 | g0044 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18942 | hp1 | a0001 | c0001 | t0024 | g0150 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18942 | hp2 | a0001 | c0001 | t0025 | g0306 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18944 | hp2 | a0001 | c0002 | t0005 | g0130 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18947 | hp2 | a0001 | c0001 | t0012 | g0123 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18948 | hp1 | a0001 | c0002 | t0005 | g0080 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18949 | hp2 | a0001 | c0001 | t0035 | g0212 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18951 | hp1 | a0001 | c0002 | t0004 | g0066 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18957 | hp2 | a0001 | c0001 | t0013 | g0106 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18961 | hp1 | a0001 | c0002 | t0005 | g0079 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18962 | hp2 | a0001 | c0002 | t0014 | g0029 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18969 | hp1 | a0001 | c0001 | t0050 | g0156 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18974 | hp2 | a0001 | c0002 | t0005 | g0282 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18975 | hp1 | a0001 | c0001 | t0033 | g0251 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18978 | hp2 | a0001 | c0001 | t0023 | g0208 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18980 | hp1 | a0001 | c0002 | t0005 | g0055 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18982 | hp2 | a0001 | c0002 | t0006 | g0279 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18983 | hp1 | a0001 | c0001 | t0025 | g0221 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0195 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18991 | hp2 | a0001 | c0002 | t0006 | g0101 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19000 | hp2 | a0004 | c0007 | t0002 | g0119 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19007 | hp2 | a0001 | c0001 | t0013 | g0111 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19030 | hp2 | a0001 | c0002 | t0009 | g0338 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0324 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0073 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19057 | hp2 | a0001 | c0002 | t0014 | g0250 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19067 | hp2 | a0001 | c0002 | t0006 | g0092 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19085 | hp2 | a0001 | c0001 | t0046 | g0172 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19091 | hp1 | a0001 | c0002 | t0005 | g0165 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA19240 | hp2 | a0001 | c0001 | t0015 | g0067 | AFR | YRI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ASW | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA20129 | hp2 | a0001 | c0001 | t0021 | g0320 | AFR | ASW | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0032 | EUR | TSI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | TSI | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA20905 | hp1 | a0001 | c0002 | t0004 | g0098 | SAS | GIH | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA20905 | hp2 | a0001 | c0002 | t0007 | g0289 | SAS | GIH | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01123 | hp1 | a0001 | c0002 | t0005 | g0045 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02109 | hp1 | a0003 | c0006 | t0017 | g0012 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02109 | hp2 | a0001 | c0001 | t0012 | g0330 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02486 | hp1 | a0004 | c0007 | t0026 | g0097 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG02559 | hp2 | a0002 | c0003 | t0010 | g0023 | AFR | ACB | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG03471 | hp2 | a0001 | c0001 | t0008 | g0036 | AFR | MSL | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | USA | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
HG06807 | hp2 | a0008 | c0015 | t0017 | g0344 | AFR | USA | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA20300 | hp1 | a0002 | c0003 | t0006 | g0028 | AFR | USA | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | USA | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA21309 | hp1 | a0001 | c0002 | t0032 | g0323 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
homoSapiens_chm13v2 | hp1 | a0007 | c0013 | t0001 | g0205 | REF | REF | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0013 | g0061 | REF | REF | CYP27C1_chr2_127178832_127225299 | CYP27C1 | chr2 | 127178832 | 127225299 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127187314
|
G | A | 1 | a0004 | 3 | HG02486.hp1 HG03130.hp1 NA19000.hp2 |
missense_variant | MODERATE | c.1571C>T | p.Thr524Met | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1600/5082 | 1571/1614 | 524/537 | chr2 | 127187314 | ||
chr2:127193842
|
C | G | 1 | a0005 | 2 | HG02896.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.1240G>C | p.Gly414Arg | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/9 | 1269/5082 | 1240/1614 | 414/537 | chr2 | 127193842 | ||
chr2:127206015
|
G | A | 1 | a0007 | 1 | homoSapiens_chm13v2.hp1 | missense_variant | MODERATE | c.358C>T | p.Arg120Cys | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/9 | 387/5082 | 358/1614 | 120/537 | chr2 | 127206015 | ||
chr2:127220110
|
G | C | 1 | a0002 | 15 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
missense_variant | MODERATE | c.161C>G | p.Pro54Arg | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 190/5082 | 161/1614 | 54/537 | chr2 | 127220110 | ||
chr2:127220111
|
G | T | 1 | a0002 | 15 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
missense_variant | MODERATE | c.160C>A | p.Pro54Thr | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 189/5082 | 160/1614 | 54/537 | chr2 | 127220111 | ||
chr2:127220143
|
G | A | 1 | a0008 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.128C>T | p.Ala43Val | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 157/5082 | 128/1614 | 43/537 | chr2 | 127220143 | ||
chr2:127220192
|
G | A | 1 | a0009 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.79C>T | p.Pro27Ser | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 108/5082 | 79/1614 | 27/537 | chr2 | 127220192 | ||
chr2:127220218
|
C | T | 1 | a0006 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.53G>A | p.Arg18Gln | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 82/5082 | 53/1614 | 18/537 | chr2 | 127220218 | ||
chr2:127220240
|
C | G | 1 | a0003 | 6 | HG02109.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.31G>C | p.Gly11Arg | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 60/5082 | 31/1614 | 11/537 | chr2 | 127220240 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127193795
|
C | T | 1 | a0001c0012 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1287G>A | p.Pro429Pro | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/9 | 1316/5082 | 1287/1614 | 429/537 | chr2 | 127193795 | ||
chr2:127193810
|
G | T | 1 | a0003c0010 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1272C>A | p.Gly424Gly | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/9 | 1301/5082 | 1272/1614 | 424/537 | chr2 | 127193810 | ||
chr2:127195478
|
A | C | 6 | a0001c0002a0001c0014a0002c0004others(3): Show | 88 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(85): Show |
synonymous_variant | LOW | c.1071T>G | p.Thr357Thr | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/9 | 1100/5082 | 1071/1614 | 357/537 | chr2 | 127195478 | ||
chr2:127199415
|
G | A | 1 | a0001c0005 | 5 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
synonymous_variant | LOW | c.1008C>T | p.Tyr336Tyr | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/9 | 1037/5082 | 1008/1614 | 336/537 | chr2 | 127199415 | ||
chr2:127220034
|
C | A | 1 | a0001c0014 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.237G>T | p.Ala79Ala | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/9 | 266/5082 | 237/1614 | 79/537 | chr2 | 127220034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127183982
|
C | G | 1 | a0001c0001t0035 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3289G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 3289 | chr2 | 127183982 | |||||
chr2:127184066
|
A | C | 1 | a0001c0001t0047 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3205T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 3205 | chr2 | 127184066 | |||||
chr2:127184222
|
T | C | 28 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(25): Show | 177 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*3049A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 3049 | chr2 | 127184222 | |||||
chr2:127184422
|
G | A | 1 | a0001c0001t0048 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2849C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2849 | chr2 | 127184422 | |||||
chr2:127184446
|
T | G | 3 | a0001c0002t0018a0002c0004t0019a0002c0004t0041 | 7 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2825A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2825 | chr2 | 127184446 | |||||
chr2:127184474
|
C | T | 3 | a0001c0002t0018a0002c0004t0019a0002c0004t0041 | 7 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2797G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2797 | chr2 | 127184474 | |||||
chr2:127184555
|
A | G | 49 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(46): Show | 233 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*2716T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2716 | chr2 | 127184555 | |||||
chr2:127184595
|
A | G | 1 | a0001c0001t0046 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2676T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2676 | chr2 | 127184595 | |||||
chr2:127184604
|
G | T | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2667 | chr2 | 127184604 | |||||
chr2:127184655
|
G | A | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0023others(12): Show | 142 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*2616C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2616 | chr2 | 127184655 | |||||
chr2:127184756
|
C | T | 2 | a0004c0007t0026a0004c0007t0027 | 2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2515G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2515 | chr2 | 127184756 | |||||
chr2:127184758
|
C | T | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | 160 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*2513G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2513 | chr2 | 127184758 | |||||
chr2:127184847
|
G | A | 2 | a0001c0002t0031a0001c0002t0037 | 2 | HG03516.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2424C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2424 | chr2 | 127184847 | |||||
chr2:127184934
|
C | T | 1 | a0001c0001t0034 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2337G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2337 | chr2 | 127184934 | |||||
chr2:127184946
|
A | C | 1 | a0001c0002t0007 | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2325T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2325 | chr2 | 127184946 | |||||
chr2:127185026
|
C | T | 2 | a0004c0007t0026a0004c0007t0027 | 2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2245G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2245 | chr2 | 127185026 | |||||
chr2:127185112
|
G | A | 1 | a0001c0001t0038 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2159C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2159 | chr2 | 127185112 | |||||
chr2:127185197
|
G | C | 1 | a0001c0002t0022 | 2 | HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2074C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2074 | chr2 | 127185197 | |||||
chr2:127185215
|
C | T | 11 | a0001c0001t0006a0001c0001t0033a0001c0001t0045others(8): Show | 42 | HG00609.hp1 HG01175.hp2 HG01192.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2056G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 2056 | chr2 | 127185215 | |||||
chr2:127185440
|
C | T | 1 | a0001c0002t0032 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1831G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1831 | chr2 | 127185440 | |||||
chr2:127185733
|
GA | G | 2 | a0002c0004t0019a0002c0004t0041 | 4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1537delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1537 | chr2 | 127185733 | |||||
chr2:127185964
|
C | T | 2 | a0001c0002t0009a0001c0002t0039 | 7 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1307G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1307 | chr2 | 127185964 | |||||
chr2:127185978
|
G | A | 5 | a0001c0001t0006a0001c0002t0004a0001c0002t0006others(2): Show | 29 | HG00609.hp1 HG01192.hp2 HG01256.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1293C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1293 | chr2 | 127185978 | |||||
chr2:127186245
|
TTTATTTA others(4): Show |
T | 2 | a0003c0006t0017a0008c0015t0017 | 3 | HG02109.hp1 HG02896.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1015_*1025delTAAA others(7): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 1015 | chr2 | 127186245 | |||||
chr2:127186302
|
A | G | 2 | a0001c0002t0011a0002c0004t0020 | 8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*969T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 969 | chr2 | 127186302 | |||||
chr2:127186344
|
G | A | 2 | a0001c0001t0010a0002c0003t0010 | 5 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*927C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 927 | chr2 | 127186344 | |||||
chr2:127186369
|
C | CATTTT | 22 | a0001c0001t0002a0001c0001t0003a0001c0001t0024others(19): Show | 126 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*897_*901dupAAAAT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 901 | chr2 | 127186369 | |||||
chr2:127186369
|
C | CATTTTAT others(3): Show |
6 | a0001c0001t0005a0001c0001t0012a0001c0001t0030others(3): Show | 19 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*892_*901dupAAAATA others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 901 | chr2 | 127186369 | |||||
chr2:127186369
|
CATTTT | C | 16 | a0001c0001t0006a0001c0001t0008a0001c0001t0010others(13): Show | 51 | HG01069.hp2 HG01168.hp2 HG01169.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*897_*901delAAAAT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 897 | chr2 | 127186369 | |||||
chr2:127186369
|
CATTTTAT others(8): Show |
C | 2 | a0003c0006t0017a0008c0015t0017 | 3 | HG02109.hp1 HG02896.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*887_*901delAAAATA others(9): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 887 | chr2 | 127186369 | |||||
chr2:127186435
|
TCA | T | 2 | a0002c0004t0019a0002c0004t0041 | 4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*834_*835delTG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 834 | chr2 | 127186435 | |||||
chr2:127186438
|
C | A | 2 | a0002c0004t0019a0002c0004t0041 | 4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*833G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 833 | chr2 | 127186438 | |||||
chr2:127186451
|
G | T | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 820 | chr2 | 127186451 | |||||
chr2:127186459
|
G | A | 3 | a0001c0002t0018a0002c0004t0019a0002c0004t0041 | 7 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*812C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 812 | chr2 | 127186459 | |||||
chr2:127186460
|
C | A | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*811G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 811 | chr2 | 127186460 | |||||
chr2:127186504
|
C | T | 1 | a0001c0001t0024 | 2 | HG02056.hp2 NA18942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*767G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 767 | chr2 | 127186504 | |||||
chr2:127186551
|
A | G | 7 | a0001c0001t0005a0001c0001t0021a0001c0001t0044others(4): Show | 20 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*720T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 720 | chr2 | 127186551 | |||||
chr2:127186681
|
G | A | 1 | a0001c0001t0023 | 2 | HG02015.hp1 NA18978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*590C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 590 | chr2 | 127186681 | |||||
chr2:127186691
|
G | A | 1 | a0001c0002t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*580C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 580 | chr2 | 127186691 | |||||
chr2:127186703
|
C | A | 1 | a0001c0001t0050 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*568G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 568 | chr2 | 127186703 | |||||
chr2:127186988
|
G | C | 3 | a0001c0002t0007a0001c0002t0011a0002c0004t0020 | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*283C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 283 | chr2 | 127186988 | |||||
chr2:127187122
|
A | G | 1 | a0001c0001t0043 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 149 | chr2 | 127187122 | |||||
chr2:127187137
|
C | T | 2 | a0004c0007t0026a0004c0007t0027 | 2 | HG02486.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*134G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 134 | chr2 | 127187137 | |||||
chr2:127187205
|
A | AC | 50 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(47): Show | 249 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(246): Show |
3_prime_UTR_variant | MODIFIER | c.*65_*66insG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 9/9 | 65 | chr2 | 127187205 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:127187447
|
C | G | 17 | a0001c0001t0005g0195a0001c0001t0021g0320a0001c0001t0021g0321others(14): Show | 17 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1498-60G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187447 | ||||||
chr2:127187511
|
C | T | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1498-124G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187511 | ||||||
chr2:127187550
|
T | G | 3 | a0001c0001t0001g0246a0001c0001t0001g0294a0001c0001t0001g0303 | 3 | HG00408.hp2 HG02083.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1498-163A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187550 | ||||||
chr2:127187729
|
G | T | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1498-342C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187729 | ||||||
chr2:127187893
|
T | C | 9 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1498-506A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127187893 | ||||||
chr2:127188025
|
C | T | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1498-638G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188025 | ||||||
chr2:127188076
|
C | A | 6 | a0001c0002t0009g0035a0001c0002t0009g0057a0001c0002t0009g0064others(3): Show | 6 | HG01884.hp1 HG01891.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-689G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188076 | ||||||
chr2:127188095
|
T | A | 10 | a0001c0001t0001g0196a0001c0001t0001g0240a0001c0001t0001g0241others(7): Show | 10 | HG01169.hp2 HG01952.hp1 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.1498-708A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188095 | ||||||
chr2:127188137
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1498-750C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188137 | ||||||
chr2:127188211
|
G | A | 163 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(160): Show | 165 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1498-824C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188211 | ||||||
chr2:127188229
|
G | C | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1498-842C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188229 | ||||||
chr2:127188310
|
G | A | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1498-923C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188310 | ||||||
chr2:127188434
|
C | T | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1498-1047G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188434 | ||||||
chr2:127188457
|
T | G | 8 | a0001c0002t0011g0047a0001c0002t0011g0049a0001c0002t0011g0050others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498-1070A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188457 | ||||||
chr2:127188475
|
C | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0046 | 2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1498-1088G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188475 | ||||||
chr2:127188522
|
GC | G | 35 | a0001c0001t0006g0073a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00609.hp1 HG01192.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.1498-1136delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188522 | ||||||
chr2:127188524
|
C | G | 35 | a0001c0001t0006g0073a0001c0002t0004g0032a0001c0002t0004g0033others(32): Show | 36 | HG00609.hp1 HG01192.hp2 HG01256.hp1 others(33): Show |
intron_variant | MODIFIER | c.1498-1137G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188524 | ||||||
chr2:127188575
|
G | A | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1498-1188C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188575 | ||||||
chr2:127188668
|
T | TTCCATCT others(321): Show |
1 | a0001c0002t0009g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1498-1282_1498-128 others(332): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188668 | ||||||
chr2:127188668
|
T | TTCCATCT others(331): Show |
3 | a0001c0002t0009g0035a0001c0002t0009g0064a0001c0002t0009g0086 | 3 | HG01884.hp1 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1498-1282_1498-128 others(342): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188668 | ||||||
chr2:127188668
|
T | TTCCATCT others(332): Show |
2 | a0001c0002t0009g0057a0001c0002t0009g0338 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1498-1282_1498-128 others(343): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188668 | ||||||
chr2:127188668
|
T | TTCCATCT others(336): Show |
1 | a0001c0002t0039g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1498-1282_1498-128 others(347): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188668 | ||||||
chr2:127188689
|
T | G | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1498-1302A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188689 | ||||||
chr2:127188750
|
T | C | 19 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(16): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1498-1363A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188750 | ||||||
chr2:127188796
|
T | C | 7 | a0001c0001t0002g0112a0001c0001t0002g0114a0001c0001t0002g0115others(4): Show | 7 | HG00642.hp2 HG00733.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1498-1409A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188796 | ||||||
chr2:127188855
|
T | G | 236 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(233): Show | 239 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(236): Show |
intron_variant | MODIFIER | c.1498-1468A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188855 | ||||||
chr2:127188867
|
G | T | 12 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1498-1480C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188867 | ||||||
chr2:127188899
|
T | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1498-1512A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188899 | ||||||
chr2:127188924
|
T | C | 20 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(17): Show | 20 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.1498-1537A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188924 | ||||||
chr2:127188943
|
G | T | 236 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(233): Show | 239 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(236): Show |
intron_variant | MODIFIER | c.1498-1556C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188943 | ||||||
chr2:127188974
|
C | T | 1 | a0001c0001t0049g0128 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1498-1587G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127188974 | ||||||
chr2:127189018
|
C | T | 1 | a0001c0002t0039g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1498-1631G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189018 | ||||||
chr2:127189019
|
A | G | 28 | a0001c0001t0006g0073a0001c0002t0004g0032a0001c0002t0004g0033others(25): Show | 29 | HG00609.hp1 HG01192.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1498-1632T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189019 | ||||||
chr2:127189028
|
C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02451.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1498-1641G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189028 | ||||||
chr2:127189082
|
C | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0263 | 2 | NA19074.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1498-1695G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189082 | ||||||
chr2:127189168
|
GC | G | 313 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(310): Show | 320 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.1498-1782delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189168 | ||||||
chr2:127189315
|
C | G | 1 | a0003c0006t0028g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1498-1928G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189315 | ||||||
chr2:127189436
|
C | A | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1498-2049G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189436 | ||||||
chr2:127189468
|
G | A | 11 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(8): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-2081C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189468 | ||||||
chr2:127189535
|
G | C | 19 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(16): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1498-2148C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189535 | ||||||
chr2:127189584
|
G | A | 1 | a0001c0001t0012g0123 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1498-2197C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189584 | ||||||
chr2:127189621
|
T | TA | 8 | a0001c0002t0011g0047a0001c0002t0011g0049a0001c0002t0011g0050others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1498-2235dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189621 | ||||||
chr2:127189621
|
TA | T | 199 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(196): Show | 202 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(199): Show |
intron_variant | MODIFIER | c.1498-2235delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189621 | ||||||
chr2:127189621
|
TAA | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0214a0001c0001t0001g0224others(4): Show | 7 | HG01256.hp2 HG02004.hp1 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.1498-2236_1498-223 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189621 | ||||||
chr2:127189661
|
G | T | 11 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(8): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1498-2274C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189661 | ||||||
chr2:127189831
|
C | T | 17 | a0001c0001t0005g0195a0001c0001t0021g0320a0001c0001t0021g0321others(14): Show | 17 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1498-2444G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189831 | ||||||
chr2:127189876
|
T | C | 35 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(32): Show | 35 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1498-2489A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189876 | ||||||
chr2:127189944
|
G | C | 1 | a0001c0001t0002g0113 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1498-2557C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127189944 | ||||||
chr2:127190133
|
G | A | 143 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(140): Show | 145 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.1498-2746C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190133 | ||||||
chr2:127190147
|
G | A | 1 | a0001c0001t0045g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1498-2760C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190147 | ||||||
chr2:127190261
|
T | TA | 8 | a0001c0002t0011g0047a0001c0002t0011g0049a0001c0002t0011g0050others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497+2832dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190261 | ||||||
chr2:127190261
|
T | TAA | 11 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(8): Show | 11 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+2831_1497+283 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190261 | ||||||
chr2:127190262
|
A | T | 12 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(9): Show | 12 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1497+2832T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190262 | ||||||
chr2:127190271
|
T | A | 19 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(16): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2823A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190271 | ||||||
chr2:127190329
|
CTCTTTTT others(4): Show |
C | 4 | a0001c0002t0009g0057a0001c0002t0009g0064a0001c0002t0009g0081others(1): Show | 4 | HG01884.hp1 HG01891.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+2754_1497+276 others(15): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190329 | ||||||
chr2:127190331
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0002t0009g0035a0001c0002t0009g0338 | 2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1497+2751_1497+276 others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190331 | ||||||
chr2:127190340
|
T | TTTC | 108 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0104others(105): Show | 109 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.1497+2753_1497+275 others(7): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190340 | ||||||
chr2:127190341
|
T | TTC | 54 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0071others(51): Show | 55 | HG01069.hp2 HG01123.hp1 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.1497+2752_1497+275 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190341 | ||||||
chr2:127190342
|
C | T | 162 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(159): Show | 164 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1497+2752G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190342 | ||||||
chr2:127190342
|
CT | C | 26 | a0001c0001t0002g0153a0001c0001t0043g0162a0001c0002t0007g0059others(23): Show | 26 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.1497+2751delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190342 | ||||||
chr2:127190342
|
CTT | C | 15 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(12): Show | 15 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1497+2750_1497+275 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190342 | ||||||
chr2:127190382
|
A | G | 19 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(16): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2712T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190382 | ||||||
chr2:127190388
|
G | A | 19 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(16): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2706C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190388 | ||||||
chr2:127190406
|
G | A | 3 | a0001c0002t0009g0057a0001c0002t0009g0064a0001c0002t0009g0086 | 3 | HG01884.hp1 HG01891.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1497+2688C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190406 | ||||||
chr2:127190428
|
T | C | 19 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(16): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2666A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190428 | ||||||
chr2:127190430
|
C | T | 10 | a0001c0002t0015g0329a0001c0002t0015g0342a0001c0002t0018g0179others(7): Show | 10 | HG02258.hp2 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1497+2664G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190430 | ||||||
chr2:127190562
|
G | A | 9 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(6): Show | 9 | HG01168.hp2 HG01169.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+2532C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190562 | ||||||
chr2:127190565
|
C | T | 11 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(8): Show | 11 | HG02145.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+2529G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190565 | ||||||
chr2:127190717
|
C | T | 1 | a0001c0001t0002g0139 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1497+2377G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190717 | ||||||
chr2:127190760
|
G | A | 324 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(321): Show | 331 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.1497+2334C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190760 | ||||||
chr2:127190804
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1497+2290C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190804 | ||||||
chr2:127190871
|
C | T | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1497+2223G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190871 | ||||||
chr2:127190940
|
TG | T | 3 | a0001c0002t0015g0329a0001c0002t0015g0342a0001c0014t0008g0343 | 3 | HG02258.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1497+2153delC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190940 | ||||||
chr2:127190941
|
G | GA | 33 | a0001c0001t0001g0225a0001c0001t0003g0034a0001c0001t0003g0187others(30): Show | 34 | HG01123.hp1 HG01243.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1497+2152dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190941 | ||||||
chr2:127190954
|
A | G | 1 | a0001c0002t0009g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1497+2140T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127190954 | ||||||
chr2:127191023
|
A | T | 19 | a0001c0002t0007g0059a0001c0002t0007g0082a0001c0002t0007g0083others(16): Show | 19 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1497+2071T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191023 | ||||||
chr2:127191045
|
G | A | 35 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(32): Show | 35 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.1497+2049C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191045 | ||||||
chr2:127191227
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1497+1867C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191227 | ||||||
chr2:127191332
|
T | G | 343 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(340): Show | 350 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.1497+1762A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191332 | ||||||
chr2:127191360
|
A | G | 1 | a0001c0005t0002g0267 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1497+1734T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191360 | ||||||
chr2:127191475
|
C | T | 3 | a0001c0002t0016g0331a0001c0002t0016g0332a0001c0002t0016g0333 | 3 | HG01175.hp2 HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1497+1619G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191475 | ||||||
chr2:127191480
|
C | T | 14 | a0001c0002t0007g0094a0001c0002t0007g0327a0001c0002t0007g0334others(11): Show | 14 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1497+1614G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191480 | ||||||
chr2:127191539
|
T | C | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497+1555A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191539 | ||||||
chr2:127191565
|
C | G | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1497+1529G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191565 | ||||||
chr2:127191622
|
A | G | 241 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(238): Show | 244 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.1497+1472T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191622 | ||||||
chr2:127191698
|
G | A | 4 | a0002c0004t0019g0014a0002c0004t0019g0015a0002c0004t0019g0016others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+1396C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191698 | ||||||
chr2:127191729
|
C | T | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1497+1365G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191729 | ||||||
chr2:127191828
|
C | T | 1 | a0001c0002t0006g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1497+1266G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191828 | ||||||
chr2:127191852
|
A | T | 1 | a0001c0002t0011g0062 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1497+1242T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191852 | ||||||
chr2:127191888
|
G | T | 1 | a0001c0001t0001g0241 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1497+1206C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191888 | ||||||
chr2:127191892
|
C | G | 1 | a0001c0002t0031g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1497+1202G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191892 | ||||||
chr2:127191929
|
A | G | 3 | a0001c0001t0002g0160a0001c0001t0002g0202a0001c0001t0002g0292 | 3 | HG00609.hp2 HG02165.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1497+1165T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127191929 | ||||||
chr2:127192093
|
C | T | 7 | a0001c0002t0015g0329a0001c0002t0015g0342a0001c0014t0008g0343others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1497+1001G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192093 | ||||||
chr2:127192201
|
C | T | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1497+893G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192201 | ||||||
chr2:127192262
|
C | G | 1 | a0001c0002t0006g0279 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1497+832G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192262 | ||||||
chr2:127192294
|
T | C | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1497+800A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192294 | ||||||
chr2:127192322
|
T | G | 10 | a0001c0002t0007g0334a0001c0002t0007g0337a0001c0002t0011g0047others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+772A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192322 | ||||||
chr2:127192374
|
A | C | 8 | a0001c0002t0016g0331a0001c0002t0016g0332a0001c0002t0016g0333others(5): Show | 8 | HG01175.hp2 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1497+720T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192374 | ||||||
chr2:127192387
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1497+707A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192387 | ||||||
chr2:127192439
|
G | T | 10 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(7): Show | 10 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1497+655C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192439 | ||||||
chr2:127192498
|
G | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(161): Show | 166 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.1497+596C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192498 | ||||||
chr2:127192554
|
G | T | 1 | a0001c0001t0001g0131 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1497+540C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192554 | ||||||
chr2:127192616
|
TC | T | 10 | a0001c0002t0007g0334a0001c0002t0007g0337a0001c0002t0011g0047others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+477delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192616 | ||||||
chr2:127192619
|
CG | C | 71 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(68): Show | 72 | HG00609.hp1 HG01168.hp2 HG01169.hp1 others(69): Show |
intron_variant | MODIFIER | c.1497+474delC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192619 | ||||||
chr2:127192619
|
CGGG | C | 138 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(135): Show | 140 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1497+472_1497+474d others(5): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192619 | ||||||
chr2:127192623
|
G | C | 57 | a0001c0002t0001g0324a0001c0002t0004g0033a0001c0002t0004g0040others(54): Show | 58 | HG00609.hp1 HG01168.hp2 HG01169.hp1 others(55): Show |
intron_variant | MODIFIER | c.1497+471C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192623 | ||||||
chr2:127192624
|
G | A | 1 | a0001c0001t0012g0330 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1497+470C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192624 | ||||||
chr2:127192624
|
G | T | 4 | a0001c0001t0002g0142a0001c0001t0002g0167a0004c0007t0026g0097others(1): Show | 4 | HG02486.hp1 HG03130.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+470C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192624 | ||||||
chr2:127192625
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0002g0099 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1497+469C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192625 | ||||||
chr2:127192625
|
G | C | 10 | a0001c0002t0007g0334a0001c0002t0007g0337a0001c0002t0011g0047others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+469C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192625 | ||||||
chr2:127192625
|
G | T | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1497+469C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192625 | ||||||
chr2:127192626
|
G | C | 16 | a0001c0001t0005g0195a0001c0002t0005g0039a0001c0002t0005g0045others(13): Show | 16 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1497+468C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192626 | ||||||
chr2:127192630
|
G | C | 10 | a0001c0002t0007g0334a0001c0002t0007g0337a0001c0002t0011g0047others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+464C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192630 | ||||||
chr2:127192675
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1497+419G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192675 | ||||||
chr2:127192751
|
G | GC | 162 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(159): Show | 164 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1497+342dupG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192751 | ||||||
chr2:127192756
|
G | GCACCGCA others(326): Show |
1 | a0001c0001t0001g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | ||||||
chr2:127192756
|
G | GCACCGCA others(326): Show |
10 | a0001c0002t0007g0334a0001c0002t0007g0337a0001c0002t0011g0047others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | ||||||
chr2:127192756
|
G | GCACCGCA others(326): Show |
10 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(7): Show | 10 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | ||||||
chr2:127192756
|
G | GCACCGCA others(326): Show |
2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | ||||||
chr2:127192756
|
G | GCACCGCA others(326): Show |
138 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(135): Show | 140 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | ||||||
chr2:127192756
|
G | GCACCGCA others(326): Show |
1 | a0001c0001t0001g0249 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1497+337_1497+338i others(335): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192756 | ||||||
chr2:127192808
|
A | T | 242 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(239): Show | 245 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(242): Show |
intron_variant | MODIFIER | c.1497+286T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192808 | ||||||
chr2:127192849
|
C | T | 8 | a0001c0002t0011g0047a0001c0002t0011g0049a0001c0002t0011g0050others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497+245G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192849 | ||||||
chr2:127192867
|
G | A | 140 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(137): Show | 142 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.1497+227C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127192867 | ||||||
chr2:127193073
|
C | T | 1 | a0001c0002t0007g0289 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1497+21G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 8/8 | chr2 | 127193073 | ||||||
chr2:127193328
|
A | T | 162 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(159): Show | 164 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1294-31T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193328 | ||||||
chr2:127193421
|
C | T | 30 | a0001c0002t0004g0032a0001c0002t0004g0033a0001c0002t0004g0040others(27): Show | 31 | HG00609.hp1 HG01168.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1294-124G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193421 | ||||||
chr2:127193449
|
C | A | 1 | a0001c0002t0031g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1294-152G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193449 | ||||||
chr2:127193449
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | HG00738.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1294-152G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193449 | ||||||
chr2:127193519
|
T | C | 151 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(148): Show | 153 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1294-222A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 7/8 | chr2 | 127193519 | ||||||
chr2:127193882
|
G | A | 165 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(162): Show | 167 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.1215-15C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127193882 | ||||||
chr2:127193883
|
C | T | 139 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(136): Show | 141 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.1215-16G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127193883 | ||||||
chr2:127193986
|
G | C | 2 | a0001c0001t0021g0320a0001c0001t0021g0321 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1215-119C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127193986 | ||||||
chr2:127193994
|
T | G | 1 | a0001c0002t0007g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1215-127A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127193994 | ||||||
chr2:127194170
|
T | C | 10 | a0001c0002t0011g0047a0001c0002t0011g0049a0001c0002t0011g0050others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1215-303A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194170 | ||||||
chr2:127194221
|
C | T | 150 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(147): Show | 152 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.1215-354G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194221 | ||||||
chr2:127194258
|
G | A | 12 | a0001c0002t0007g0334a0001c0002t0007g0337a0001c0002t0011g0047others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1215-391C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194258 | ||||||
chr2:127194505
|
C | T | 163 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(160): Show | 165 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1215-638G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194505 | ||||||
chr2:127194555
|
G | A | 2 | a0001c0001t0021g0320a0001c0001t0021g0321 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1215-688C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194555 | ||||||
chr2:127194617
|
A | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(160): Show | 165 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1214+718T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194617 | ||||||
chr2:127194630
|
A | G | 163 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(160): Show | 165 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1214+705T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194630 | ||||||
chr2:127194687
|
T | C | 163 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(160): Show | 165 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1214+648A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194687 | ||||||
chr2:127194710
|
G | A | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1214+625C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194710 | ||||||
chr2:127194842
|
C | CT | 85 | a0001c0001t0001g0281a0001c0002t0001g0324a0001c0002t0004g0032others(82): Show | 86 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(83): Show |
intron_variant | MODIFIER | c.1214+492dupA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194842 | ||||||
chr2:127194868
|
C | T | 163 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(160): Show | 165 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.1214+467G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194868 | ||||||
chr2:127194885
|
G | C | 9 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1214+450C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194885 | ||||||
chr2:127194956
|
A | C | 151 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(148): Show | 153 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.1214+379T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194956 | ||||||
chr2:127194997
|
T | G | 7 | a0001c0002t0015g0329a0001c0002t0015g0342a0001c0014t0008g0343others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1214+338A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127194997 | ||||||
chr2:127195249
|
G | A | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1214+86C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 6/8 | chr2 | 127195249 | ||||||
chr2:127195582
|
C | T | 12 | a0001c0002t0007g0334a0001c0002t0007g0337a0001c0002t0011g0047others(9): Show | 12 | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1048-81G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127195582 | ||||||
chr2:127195841
|
G | A | 152 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(149): Show | 154 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.1048-340C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127195841 | ||||||
chr2:127195879
|
G | A | 7 | a0001c0002t0015g0329a0001c0002t0015g0342a0001c0014t0008g0343others(4): Show | 7 | HG02258.hp2 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1048-378C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127195879 | ||||||
chr2:127195950
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1048-449C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127195950 | ||||||
chr2:127196019
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1048-518T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196019 | ||||||
chr2:127196065
|
CT | C | 86 | a0001c0001t0002g0238a0001c0002t0001g0324a0001c0002t0004g0032others(83): Show | 87 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(84): Show |
intron_variant | MODIFIER | c.1048-565delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196065 | ||||||
chr2:127196065
|
CTT | C | 153 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(150): Show | 155 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.1048-566_1048-565d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196065 | ||||||
chr2:127196080
|
T | C | 29 | a0001c0002t0005g0039a0001c0002t0005g0045a0001c0002t0005g0055others(26): Show | 29 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1048-579A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196080 | ||||||
chr2:127196124
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1048-623C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196124 | ||||||
chr2:127196212
|
A | G | 29 | a0001c0002t0005g0039a0001c0002t0005g0045a0001c0002t0005g0055others(26): Show | 29 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1048-711T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196212 | ||||||
chr2:127196224
|
G | A | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-723C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196224 | ||||||
chr2:127196262
|
C | CTG | 241 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(238): Show | 244 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(241): Show |
intron_variant | MODIFIER | c.1048-763_1048-762d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196262 | ||||||
chr2:127196298
|
G | C | 1 | a0001c0001t0001g0219 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048-797C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196298 | ||||||
chr2:127196318
|
C | T | 29 | a0001c0002t0005g0039a0001c0002t0005g0045a0001c0002t0005g0055others(26): Show | 29 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1048-817G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196318 | ||||||
chr2:127196356
|
C | T | 1 | a0003c0006t0028g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1048-855G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196356 | ||||||
chr2:127196445
|
G | A | 29 | a0001c0002t0005g0039a0001c0002t0005g0045a0001c0002t0005g0055others(26): Show | 29 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1048-944C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196445 | ||||||
chr2:127196464
|
T | C | 1 | a0001c0001t0015g0067 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1048-963A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196464 | ||||||
chr2:127196533
|
CA | C | 230 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(227): Show | 233 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(230): Show |
intron_variant | MODIFIER | c.1048-1033delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196533 | ||||||
chr2:127196983
|
A | AT | 6 | a0001c0002t0005g0039a0001c0002t0005g0055a0001c0002t0005g0056others(3): Show | 6 | HG02027.hp2 HG02074.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1048-1483_1048-148 others(5): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127196983 | ||||||
chr2:127197046
|
A | G | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-1545T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197046 | ||||||
chr2:127197063
|
G | C | 1 | a0001c0001t0002g0238 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1048-1562C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197063 | ||||||
chr2:127197221
|
A | G | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-1720T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197221 | ||||||
chr2:127197370
|
C | T | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-1869G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197370 | ||||||
chr2:127197414
|
C | T | 2 | a0004c0007t0026g0097a0004c0007t0027g0095 | 2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1048-1913G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197414 | ||||||
chr2:127197438
|
G | A | 19 | a0001c0002t0005g0039a0001c0002t0005g0045a0001c0002t0005g0055others(16): Show | 19 | HG01123.hp1 HG01891.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1048-1937C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197438 | ||||||
chr2:127197441
|
G | A | 25 | a0001c0002t0005g0039a0001c0002t0005g0045a0001c0002t0005g0055others(22): Show | 25 | HG01123.hp1 HG01243.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1047+1935C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197441 | ||||||
chr2:127197442
|
C | G | 1 | a0001c0001t0001g0266 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1047+1934G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197442 | ||||||
chr2:127197660
|
C | T | 2 | a0001c0001t0003g0325a0001c0001t0008g0326 | 2 | HG01884.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1047+1716G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197660 | ||||||
chr2:127197706
|
A | G | 1 | a0003c0010t0029g0011 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1047+1670T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197706 | ||||||
chr2:127197782
|
C | A | 1 | a0001c0002t0006g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1047+1594G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197782 | ||||||
chr2:127197784
|
A | G | 6 | a0001c0002t0016g0331a0001c0002t0016g0332a0001c0002t0016g0333others(3): Show | 6 | HG01175.hp2 HG02257.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1047+1592T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197784 | ||||||
chr2:127197867
|
C | T | 13 | a0001c0002t0005g0039a0001c0002t0005g0045a0001c0002t0005g0055others(10): Show | 13 | HG01123.hp1 HG02027.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1047+1509G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197867 | ||||||
chr2:127197932
|
G | A | 1 | a0003c0006t0017g0010 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1047+1444C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127197932 | ||||||
chr2:127198073
|
T | C | 1 | a0001c0001t0001g0006 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1047+1303A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198073 | ||||||
chr2:127198110
|
G | A | 4 | a0002c0004t0019g0014a0002c0004t0019g0015a0002c0004t0019g0016others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+1266C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198110 | ||||||
chr2:127198128
|
T | C | 1 | a0001c0001t0021g0321 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1047+1248A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198128 | ||||||
chr2:127198184
|
G | GACACACA others(3): Show |
3 | a0001c0002t0009g0057a0001c0002t0009g0064a0001c0002t0042g0044 | 3 | HG01884.hp1 HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1047+1191_1047+119 others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198184 | ||||||
chr2:127198184
|
G | GACACACA others(5): Show |
1 | a0001c0002t0009g0086 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1047+1191_1047+119 others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198184 | ||||||
chr2:127198186
|
T | C | 7 | a0001c0001t0001g0071a0001c0002t0009g0035a0001c0002t0009g0057others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047+1190A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198186
|
T | TAC | 8 | a0001c0001t0001g0110a0001c0001t0002g0135a0001c0001t0002g0149others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1047+1188_1047+118 others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198186
|
T | TACAC | 4 | a0001c0001t0001g0224a0001c0002t0018g0179a0001c0002t0018g0194others(1): Show | 4 | HG01256.hp2 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1047+1186_1047+118 others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198186
|
T | TACACAC | 48 | a0001c0001t0001g0030a0001c0001t0001g0046a0001c0001t0001g0096others(45): Show | 49 | HG01069.hp2 HG01175.hp1 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.1047+1184_1047+118 others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198186
|
T | TACACACA others(1): Show |
125 | a0001c0001t0001g0006a0001c0001t0001g0103a0001c0001t0001g0104others(122): Show | 127 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1047+1182_1047+118 others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198186
|
T | TACACACA others(3): Show |
26 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0254others(23): Show | 26 | HG00609.hp1 HG00642.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.1047+1180_1047+118 others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198186
|
T | TACACACA others(5): Show |
18 | a0001c0001t0001g0233a0001c0001t0001g0240a0001c0001t0001g0241others(15): Show | 18 | HG01169.hp2 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1047+1178_1047+118 others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198186
|
T | TACACACA others(9): Show |
1 | a0001c0001t0001g0196 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1047+1174_1047+118 others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198186
|
TACAC | T | 9 | a0001c0001t0002g0058a0001c0001t0002g0078a0001c0001t0002g0084others(6): Show | 9 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1047+1186_1047+118 others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198186 | ||||||
chr2:127198475
|
T | C | 9 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(6): Show | 9 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1047+901A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198475 | ||||||
chr2:127198542
|
CT | C | 54 | a0001c0002t0004g0032a0001c0002t0004g0033a0001c0002t0004g0040others(51): Show | 55 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.1047+833delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198542 | ||||||
chr2:127198577
|
A | ATGTTTTG others(41): Show |
1 | a0001c0001t0002g0157 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1047+751_1047+798d others(50): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198577 | ||||||
chr2:127198622
|
A | C | 1 | a0001c0001t0001g0236 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1047+754T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198622 | ||||||
chr2:127198628
|
T | C | 3 | a0001c0002t0016g0331a0001c0002t0016g0332a0001c0002t0016g0333 | 3 | HG01175.hp2 HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1047+748A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198628 | ||||||
chr2:127198638
|
T | A | 1 | a0001c0001t0002g0161 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1047+738A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198638 | ||||||
chr2:127198676
|
A | C | 52 | a0001c0002t0004g0032a0001c0002t0004g0033a0001c0002t0004g0040others(49): Show | 53 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(50): Show |
intron_variant | MODIFIER | c.1047+700T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198676 | ||||||
chr2:127198693
|
T | C | 3 | a0003c0006t0017g0010a0003c0006t0017g0012a0008c0015t0017g0344 | 3 | HG02109.hp1 HG02896.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1047+683A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198693 | ||||||
chr2:127198833
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0281a0001c0001t0001g0293 | 3 | HG02040.hp1 HG04184.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1047+543G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198833 | ||||||
chr2:127198835
|
C | T | 3 | a0001c0002t0018g0179a0001c0002t0018g0194a0001c0002t0018g0223 | 3 | HG02615.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1047+541G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198835 | ||||||
chr2:127198871
|
C | A | 1 | a0001c0002t0037g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1047+505G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198871 | ||||||
chr2:127198967
|
A | G | 49 | a0001c0002t0004g0032a0001c0002t0004g0033a0001c0002t0004g0040others(46): Show | 50 | HG00609.hp1 HG01123.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.1047+409T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127198967 | ||||||
chr2:127199002
|
C | T | 1 | a0003c0006t0028g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1047+374G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199002 | ||||||
chr2:127199015
|
T | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0281 | 2 | HG04184.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1047+361A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199015 | ||||||
chr2:127199055
|
C | A | 3 | a0001c0002t0018g0179a0001c0002t0018g0194a0001c0002t0018g0223 | 3 | HG02615.hp2 HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1047+321G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199055 | ||||||
chr2:127199111
|
C | A | 3 | a0002c0004t0020g0020a0002c0004t0020g0021a0002c0004t0020g0022 | 3 | HG03041.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1047+265G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199111 | ||||||
chr2:127199156
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1047+220C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199156 | ||||||
chr2:127199236
|
G | A | 141 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0096others(138): Show | 143 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.1047+140C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199236 | ||||||
chr2:127199319
|
G | T | 1 | a0001c0002t0004g0053 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1047+57C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 5/8 | chr2 | 127199319 | ||||||
chr2:127199607
|
C | T | 5 | a0001c0002t0001g0324a0001c0002t0007g0327a0001c0002t0015g0329others(2): Show | 5 | HG02258.hp2 HG03041.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-68G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127199607 | ||||||
chr2:127199708
|
C | T | 5 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(2): Show | 5 | HG02622.hp1 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-169G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127199708 | ||||||
chr2:127199747
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.884-208C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127199747 | ||||||
chr2:127199852
|
C | A | 134 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0103others(131): Show | 136 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.884-313G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127199852 | ||||||
chr2:127200066
|
G | A | 1 | a0008c0015t0017g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.884-527C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200066 | ||||||
chr2:127200128
|
C | T | 9 | a0002c0003t0003g0024a0002c0003t0006g0026a0002c0003t0006g0027others(6): Show | 9 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.884-589G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200128 | ||||||
chr2:127200169
|
G | A | 5 | a0001c0001t0001g0096a0001c0001t0021g0320a0001c0001t0021g0321others(2): Show | 5 | HG02451.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-630C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200169 | ||||||
chr2:127200242
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.884-703T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200242 | ||||||
chr2:127200465
|
C | A | 287 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0071others(284): Show | 293 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(290): Show |
intron_variant | MODIFIER | c.883+657G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200465 | ||||||
chr2:127200941
|
C | T | 105 | a0001c0001t0001g0110a0001c0001t0001g0143a0001c0001t0001g0144others(102): Show | 109 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.883+181G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 4/8 | chr2 | 127200941 | ||||||
chr2:127201414
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.674-83A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127201414 | ||||||
chr2:127201488
|
G | T | 2 | a0001c0001t0002g0078a0001c0001t0002g0099 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.674-157C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127201488 | ||||||
chr2:127201883
|
C | A | 8 | a0002c0003t0003g0024a0002c0003t0006g0026a0002c0003t0006g0027others(5): Show | 8 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.674-552G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127201883 | ||||||
chr2:127201921
|
A | G | 2 | a0001c0002t0007g0335a0001c0002t0007g0336 | 2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.674-590T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127201921 | ||||||
chr2:127202039
|
A | T | 1 | a0003c0006t0028g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674-708T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202039 | ||||||
chr2:127202067
|
C | A | 1 | a0001c0001t0049g0128 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.674-736G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202067 | ||||||
chr2:127202084
|
A | AT | 102 | a0001c0001t0001g0110a0001c0001t0001g0143a0001c0001t0001g0144others(99): Show | 106 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.674-754dupA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202084 | ||||||
chr2:127202084
|
A | ATT | 15 | a0001c0001t0002g0115a0001c0001t0002g0311a0001c0005t0002g0031others(12): Show | 15 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.674-755_674-754dup others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202084 | ||||||
chr2:127202084
|
AT | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0312a0001c0002t0018g0179others(2): Show | 6 | HG01516.hp2 HG01517.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.674-754delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202084 | ||||||
chr2:127202156
|
C | G | 1 | a0003c0006t0028g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.674-825G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202156 | ||||||
chr2:127202255
|
T | G | 115 | a0001c0001t0001g0110a0001c0001t0001g0143a0001c0001t0001g0144others(112): Show | 119 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.674-924A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202255 | ||||||
chr2:127202258
|
G | A | 107 | a0001c0001t0001g0110a0001c0001t0001g0143a0001c0001t0001g0144others(104): Show | 111 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.674-927C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202258 | ||||||
chr2:127202617
|
G | C | 5 | a0001c0002t0016g0331a0001c0002t0016g0332a0001c0002t0016g0333others(2): Show | 5 | HG01175.hp2 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+755C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202617 | ||||||
chr2:127202675
|
C | G | 3 | a0001c0002t0015g0329a0001c0002t0015g0342a0001c0014t0008g0343 | 3 | HG02258.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.673+697G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202675 | ||||||
chr2:127202743
|
GT | G | 10 | a0001c0001t0001g0071a0001c0001t0002g0105a0001c0002t0009g0057others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.673+628delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202743 | ||||||
chr2:127202744
|
T | G | 2 | a0001c0001t0021g0320a0001c0001t0021g0321 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.673+628A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202744 | ||||||
chr2:127202747
|
T | A | 1 | a0001c0002t0005g0041 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.673+625A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202747 | ||||||
chr2:127202906
|
T | C | 2 | a0001c0001t0002g0159a0007c0013t0001g0205 | 2 | NA18982.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.673+466A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202906 | ||||||
chr2:127202915
|
T | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0240 | 2 | HG01952.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.673+457A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202915 | ||||||
chr2:127202948
|
C | G | 4 | a0001c0001t0021g0320a0001c0001t0021g0321a0001c0002t0009g0081others(1): Show | 4 | HG02615.hp1 HG02809.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+424G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202948 | ||||||
chr2:127202972
|
G | T | 1 | a0001c0001t0049g0128 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.673+400C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202972 | ||||||
chr2:127202976
|
T | G | 4 | a0001c0001t0008g0036a0001c0001t0008g0051a0001c0001t0008g0054others(1): Show | 5 | HG01256.hp1 HG01258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+396A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202976 | ||||||
chr2:127202993
|
A | C | 3 | a0001c0001t0047g0038a0001c0002t0006g0042a0001c0002t0006g0091 | 3 | HG00423.hp1 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.673+379T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202993 | ||||||
chr2:127202995
|
T | C | 2 | a0001c0002t0006g0042a0001c0002t0006g0091 | 2 | HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.673+377A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127202995 | ||||||
chr2:127203004
|
T | G | 1 | a0001c0001t0002g0001 | 3 | HG00738.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.673+368A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203004 | ||||||
chr2:127203090
|
C | T | 13 | a0001c0001t0003g0325a0001c0001t0008g0326a0001c0002t0001g0324others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.673+282G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203090 | ||||||
chr2:127203107
|
G | T | 3 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0337 | 3 | HG01891.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.673+265C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203107 | ||||||
chr2:127203108
|
C | T | 3 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0337 | 3 | HG01891.hp2 HG02257.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.673+264G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203108 | ||||||
chr2:127203117
|
A | G | 3 | a0001c0002t0015g0329a0001c0002t0015g0342a0001c0014t0008g0343 | 3 | HG02258.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.673+255T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203117 | ||||||
chr2:127203169
|
G | GA | 103 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(100): Show | 108 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.673+202dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203169 | ||||||
chr2:127203169
|
GA | G | 8 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0002g0239others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.673+202delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 3/8 | chr2 | 127203169 | ||||||
chr2:127203694
|
A | G | 2 | a0001c0002t0016g0332a0001c0002t0016g0333 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.474-123T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203694 | ||||||
chr2:127203729
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.474-158C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203729 | ||||||
chr2:127203828
|
T | C | 2 | a0001c0002t0001g0324a0001c0002t0007g0327 | 2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.474-257A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203828 | ||||||
chr2:127203864
|
T | C | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-293A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203864 | ||||||
chr2:127203903
|
G | A | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474-332C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203903 | ||||||
chr2:127203915
|
T | A | 1 | a0001c0002t0004g0088 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.474-344A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127203915 | ||||||
chr2:127204015
|
A | G | 1 | a0001c0002t0018g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.474-444T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204015 | ||||||
chr2:127204031
|
A | C | 1 | a0001c0002t0018g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.474-460T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204031 | ||||||
chr2:127204253
|
G | A | 3 | a0001c0002t0018g0179a0003c0006t0017g0010a0003c0006t0017g0012 | 3 | HG02109.hp1 HG02896.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.474-682C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204253 | ||||||
chr2:127204282
|
A | AAG | 9 | a0001c0001t0001g0200a0001c0001t0003g0328a0001c0002t0009g0081others(6): Show | 9 | HG01175.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-713_474-712dup others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204282 | ||||||
chr2:127204282
|
A | G | 2 | a0001c0002t0006g0042a0001c0002t0006g0091 | 2 | HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.474-711T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204282 | ||||||
chr2:127204320
|
A | AGGAG | 93 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(90): Show | 98 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.474-753_474-750dup others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204320 | ||||||
chr2:127204320
|
A | AGGAGGGA others(1): Show |
27 | a0001c0001t0044g0177a0001c0002t0007g0327a0001c0002t0007g0334others(24): Show | 27 | HG01175.hp2 HG01243.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.474-757_474-750dup others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204320 | ||||||
chr2:127204320
|
A | AGGAGGGA others(9): Show |
1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474-765_474-750dup others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204320 | ||||||
chr2:127204320
|
A | G | 2 | a0001c0001t0001g0265a0001c0001t0002g0113 | 2 | HG02300.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.474-749T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204320 | ||||||
chr2:127204346
|
A | G | 1 | a0004c0007t0002g0119 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.474-775T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204346 | ||||||
chr2:127204347
|
G | A | 1 | a0004c0007t0002g0119 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.474-776C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204347 | ||||||
chr2:127204350
|
A | AG | 7 | a0001c0001t0001g0199a0001c0001t0001g0275a0001c0001t0002g0173others(4): Show | 7 | HG01192.hp1 HG01934.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-780dupC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204350 | ||||||
chr2:127204377
|
GAGAA | G | 8 | a0001c0001t0003g0187a0001c0001t0003g0191a0001c0001t0003g0215others(5): Show | 9 | HG02055.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-810_474-807del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204377 | ||||||
chr2:127204388
|
AAAAG | A | 17 | a0002c0003t0003g0024a0002c0003t0006g0026a0002c0003t0006g0027others(14): Show | 17 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.474-821_474-818del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204388 | ||||||
chr2:127204394
|
AAGAG | A | 82 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(79): Show | 87 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.474-827_474-824del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204394 | ||||||
chr2:127204421
|
G | C | 2 | a0001c0001t0002g0164a0001c0001t0002g0175 | 2 | HG00735.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.474-850C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204421 | ||||||
chr2:127204423
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0002g0102 | 2 | NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.474-852C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204423 | ||||||
chr2:127204430
|
G | A | 1 | a0001c0001t0002g0102 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.474-859C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204430 | ||||||
chr2:127204432
|
A | G | 1 | a0001c0001t0001g0281 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.474-861T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204432 | ||||||
chr2:127204440
|
A | AAAAG | 7 | a0001c0001t0021g0321a0001c0002t0004g0098a0001c0002t0005g0076others(4): Show | 7 | HG01346.hp2 HG02486.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-873_474-870dup others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
A | AAAAGAAA others(1): Show |
10 | a0001c0001t0047g0038a0001c0002t0004g0040a0001c0002t0004g0053others(7): Show | 10 | HG00423.hp1 HG01168.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-877_474-870dup others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
A | AAAAGAAA others(5): Show |
10 | a0001c0002t0004g0032a0001c0002t0004g0068a0001c0002t0005g0041others(7): Show | 10 | HG01891.hp1 HG02809.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-881_474-870dup others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
A | AAAAGAAA others(9): Show |
2 | a0001c0002t0005g0039a0001c0002t0006g0092 | 2 | HG02027.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.474-885_474-870dup others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
A | AAAAGAAA others(17): Show |
1 | a0001c0002t0005g0045 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.474-893_474-870dup others(24): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
A | AAGAAAGA others(11): Show |
1 | a0001c0001t0021g0320 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.474-870_474-869ins others(18): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
A | G | 1 | a0001c0001t0001g0281 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.474-869T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
AAAAG | A | 12 | a0001c0001t0001g0046a0001c0001t0001g0096a0001c0001t0001g0180others(9): Show | 12 | HG01243.hp2 HG01255.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.474-873_474-870del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
AAAAGAAA others(1): Show |
A | 40 | a0001c0001t0001g0006a0001c0001t0001g0071a0001c0001t0001g0189others(37): Show | 42 | HG00408.hp1 HG00438.hp2 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.474-877_474-870del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
AAAAGAAA others(5): Show |
A | 14 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0213others(11): Show | 14 | HG01515.hp2 HG01952.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.474-881_474-870del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
AAAAGAAA others(9): Show |
A | 1 | a0001c0002t0016g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.474-885_474-870del others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
AAAAGAAA others(13): Show |
A | 4 | a0001c0001t0001g0207a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | NA18950.hp2 NA18984.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-889_474-870del others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204440
|
AAAAGAAA others(17): Show |
A | 2 | a0001c0001t0038g0339a0001c0002t0009g0338 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.474-893_474-870del others(24): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204440 | ||||||
chr2:127204443
|
A | G | 1 | a0003c0008t0008g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-872T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204443 | ||||||
chr2:127204448
|
G | GAAAGA | 3 | a0001c0001t0001g0110a0001c0001t0002g0109a0001c0001t0002g0135 | 3 | HG00423.hp2 HG03490.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.474-882_474-878dup others(5): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204448 | ||||||
chr2:127204451
|
A | G | 1 | a0003c0008t0008g0008 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.474-880T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204451 | ||||||
chr2:127204452
|
G | GA | 40 | a0001c0001t0001g0143a0001c0001t0001g0169a0001c0001t0002g0003others(37): Show | 42 | HG00438.hp1 HG00558.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.474-882dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204452 | ||||||
chr2:127204453
|
AAAG | A | 30 | a0001c0001t0001g0144a0001c0001t0002g0001a0001c0001t0002g0004others(27): Show | 33 | HG00280.hp1 HG00280.hp2 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.474-885_474-883del others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204453 | ||||||
chr2:127204453
|
AAAGAAAG | A | 7 | a0001c0001t0001g0131a0001c0001t0001g0137a0001c0001t0002g0158others(4): Show | 7 | HG00639.hp1 HG02132.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-889_474-883del others(7): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204453 | ||||||
chr2:127204456
|
GAAAGAAA others(4): Show |
G | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG00558.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.474-896_474-886del others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204456 | ||||||
chr2:127204458
|
AAGAAAGA others(90): Show |
A | 1 | a0001c0002t0018g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.474-984_474-888del others(97): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204458 | ||||||
chr2:127204461
|
AAAGAAAG others(25): Show |
A | 1 | a0001c0002t0009g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.474-922_474-891del others(32): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204461 | ||||||
chr2:127204463
|
A | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0312 | 2 | HG01192.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.474-892T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204463 | ||||||
chr2:127204464
|
GAAA | G | 4 | a0001c0001t0001g0291a0001c0001t0001g0340a0001c0001t0002g0292others(1): Show | 4 | HG00544.hp1 HG02717.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-896_474-894del others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204464 | ||||||
chr2:127204467
|
A | AG | 44 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0200others(41): Show | 44 | HG00642.hp2 HG00738.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.474-897dupC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204467 | ||||||
chr2:127204467
|
A | G | 4 | a0001c0001t0001g0199a0001c0001t0001g0312a0001c0001t0001g0341others(1): Show | 4 | HG01192.hp1 HG01934.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-896T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204467 | ||||||
chr2:127204468
|
GAAA | G | 20 | a0001c0001t0001g0188a0001c0001t0001g0193a0001c0001t0001g0198others(17): Show | 20 | HG00408.hp2 HG01169.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.474-900_474-898del others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204468 | ||||||
chr2:127204468
|
GAAAGAAA others(44): Show |
G | 1 | a0001c0001t0001g0224 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.474-948_474-898del others(51): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204468 | ||||||
chr2:127204469
|
A | G | 4 | a0001c0001t0001g0183a0001c0001t0001g0264a0001c0001t0002g0182others(1): Show | 4 | HG00735.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-898T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204469 | ||||||
chr2:127204469
|
AAAGAAAG others(13): Show |
A | 1 | a0003c0008t0008g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.474-918_474-899del others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204469 | ||||||
chr2:127204471
|
A | G | 54 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0199others(51): Show | 54 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.474-900T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204471 | ||||||
chr2:127204473
|
A | G | 18 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(15): Show | 18 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.474-902T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204473 | ||||||
chr2:127204475
|
A | G | 74 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0188others(71): Show | 74 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.474-904T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204475 | ||||||
chr2:127204477
|
A | G | 55 | a0001c0001t0001g0006a0001c0001t0001g0180a0001c0001t0001g0181others(52): Show | 57 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.474-906T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204477 | ||||||
chr2:127204479
|
A | G | 72 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0188others(69): Show | 72 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.474-908T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204479 | ||||||
chr2:127204481
|
A | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0180a0001c0001t0001g0181others(70): Show | 75 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.474-910T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204481 | ||||||
chr2:127204483
|
A | G | 19 | a0001c0001t0001g0188a0001c0001t0001g0193a0001c0001t0001g0198others(16): Show | 19 | HG00408.hp2 HG01169.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.474-912T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204483 | ||||||
chr2:127204484
|
G | A | 3 | a0001c0001t0001g0264a0001c0001t0002g0182a0006c0011t0002g0013 | 3 | HG00735.hp2 HG01168.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.474-913C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204484 | ||||||
chr2:127204485
|
A | AAAGAAAG others(12): Show |
1 | a0001c0002t0005g0056 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.474-915_474-914ins others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
A | AAAGAAAG others(25): Show |
1 | a0001c0001t0003g0325 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.474-915_474-914ins others(32): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
A | AAAGAAAG others(13): Show |
1 | a0001c0002t0005g0080 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.474-915_474-914ins others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
A | AAAGAAAG others(17): Show |
1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.474-915_474-914ins others(24): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
A | AAAGAAAG others(21): Show |
2 | a0001c0001t0008g0326a0001c0002t0001g0324 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.474-915_474-914ins others(28): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
A | AAAGAAAG others(9): Show |
1 | a0001c0002t0039g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.474-915_474-914ins others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
A | AAAGAAAG others(7): Show |
1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.474-915_474-914ins others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
A | G | 79 | a0001c0001t0001g0006a0001c0001t0001g0180a0001c0001t0001g0181others(76): Show | 81 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.474-914T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
AAAGG | A | 3 | a0001c0002t0004g0052a0001c0002t0004g0072a0001c0002t0004g0088 | 3 | HG01192.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.474-918_474-915del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204485
|
AAAGGAAG others(1): Show |
A | 3 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148 | 3 | HG01255.hp2 HG02486.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.474-922_474-915del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204485 | ||||||
chr2:127204487
|
AG | A | 70 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0188others(67): Show | 70 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.474-917delC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204487 | ||||||
chr2:127204488
|
G | A | 11 | a0001c0001t0001g0183a0001c0001t0001g0203a0001c0001t0001g0284others(8): Show | 11 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.474-917C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204488 | ||||||
chr2:127204488
|
G | GAAAGAAA others(4): Show |
1 | a0001c0002t0007g0083 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.474-918_474-917ins others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204488 | ||||||
chr2:127204489
|
G | A | 106 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(103): Show | 111 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.474-918C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204489 | ||||||
chr2:127204492
|
G | A | 72 | a0001c0001t0001g0006a0001c0001t0001g0180a0001c0001t0001g0181others(69): Show | 74 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.474-921C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204492 | ||||||
chr2:127204493
|
G | A | 80 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(77): Show | 83 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.474-922C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204493 | ||||||
chr2:127204496
|
G | A | 55 | a0001c0001t0001g0006a0001c0001t0001g0189a0001c0001t0001g0192others(52): Show | 57 | HG00408.hp1 HG00438.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.474-925C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204496 | ||||||
chr2:127204497
|
G | A | 30 | a0001c0001t0002g0003a0001c0001t0002g0112a0001c0001t0002g0113others(27): Show | 31 | HG00280.hp2 HG00733.hp1 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.474-926C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204497 | ||||||
chr2:127204500
|
G | A | 81 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0143others(78): Show | 81 | HG00558.hp2 HG00642.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.474-929C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204500 | ||||||
chr2:127204501
|
G | A | 9 | a0001c0001t0002g0112a0001c0001t0002g0118a0001c0001t0002g0135others(6): Show | 9 | HG01516.hp1 HG01891.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-930C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204501 | ||||||
chr2:127204504
|
G | A | 123 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0143others(120): Show | 125 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.474-933C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204504 | ||||||
chr2:127204505
|
G | A | 3 | a0001c0001t0002g0112a0001c0001t0002g0135a0003c0006t0017g0012 | 3 | HG01516.hp1 HG02109.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.474-934C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204505 | ||||||
chr2:127204508
|
A | G | 68 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0196others(65): Show | 69 | HG00639.hp2 HG00733.hp1 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.474-937T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204508 | ||||||
chr2:127204512
|
A | G | 43 | a0001c0001t0001g0169a0001c0001t0001g0207a0001c0001t0001g0236others(40): Show | 45 | HG00558.hp1 HG00639.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.474-941T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204512 | ||||||
chr2:127204513
|
G | GA | 3 | a0001c0002t0007g0334a0003c0006t0017g0010a0003c0006t0028g0009 | 3 | HG02257.hp1 HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.474-943dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204513 | ||||||
chr2:127204515
|
A | G | 3 | a0001c0001t0001g0263a0001c0001t0001g0314a0001c0001t0001g0341 | 3 | HG01928.hp2 HG03471.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.474-944T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204515 | ||||||
chr2:127204516
|
G | A | 202 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0104others(199): Show | 207 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(204): Show |
intron_variant | MODIFIER | c.474-945C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204516 | ||||||
chr2:127204516
|
GGAAA | G | 10 | a0001c0001t0001g0137a0001c0001t0002g0127a0001c0001t0002g0134others(7): Show | 10 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.474-949_474-946del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204516 | ||||||
chr2:127204519
|
A | G | 10 | a0001c0001t0001g0199a0001c0001t0001g0262a0001c0001t0001g0263others(7): Show | 10 | HG01069.hp2 HG01192.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.474-948T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204519 | ||||||
chr2:127204520
|
A | G | 16 | a0001c0001t0002g0003a0001c0001t0002g0105a0001c0001t0002g0113others(13): Show | 17 | HG00733.hp1 HG01981.hp1 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.474-949T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204520 | ||||||
chr2:127204521
|
GAA | G | 3 | a0001c0001t0001g0198a0001c0001t0001g0312a0001c0002t0014g0250 | 3 | NA19000.hp1 NA19057.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.474-952_474-951del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204521 | ||||||
chr2:127204523
|
A | G | 28 | a0001c0001t0001g0030a0001c0001t0001g0199a0001c0001t0001g0224others(25): Show | 28 | HG00408.hp2 HG00558.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.474-952T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204523 | ||||||
chr2:127204524
|
A | G | 11 | a0001c0001t0002g0084a0001c0001t0002g0117a0001c0001t0002g0118others(8): Show | 11 | HG00639.hp2 HG01070.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.474-953T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204524 | ||||||
chr2:127204525
|
GAA | G | 12 | a0001c0001t0001g0104a0001c0001t0001g0210a0001c0001t0001g0219others(9): Show | 12 | HG00544.hp2 HG01928.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.474-956_474-955del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204525 | ||||||
chr2:127204526
|
A | G | 1 | a0001c0001t0050g0156 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.474-955T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204526 | ||||||
chr2:127204527
|
A | G | 74 | a0001c0001t0001g0030a0001c0001t0001g0143a0001c0001t0001g0144others(71): Show | 74 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.474-956T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204527 | ||||||
chr2:127204527
|
AAGAAAGA others(5): Show |
A | 1 | a0001c0001t0002g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.474-968_474-957del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204527 | ||||||
chr2:127204528
|
A | G | 6 | a0001c0001t0002g0058a0001c0001t0002g0112a0001c0001t0002g0135others(3): Show | 6 | HG01081.hp1 HG01516.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-957T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204528 | ||||||
chr2:127204529
|
GAA | G | 9 | a0001c0001t0001g0193a0001c0001t0001g0222a0001c0001t0001g0247others(6): Show | 9 | HG00438.hp2 HG01169.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-960_474-959del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204529 | ||||||
chr2:127204530
|
AAAGAAAG others(4): Show |
A | 1 | a0001c0001t0002g0132 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.474-970_474-960del others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204530 | ||||||
chr2:127204531
|
A | G | 118 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0143others(115): Show | 122 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.474-960T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204531 | ||||||
chr2:127204531
|
AAGAAAGA others(1): Show |
A | 4 | a0001c0001t0002g0148a0001c0001t0002g0178a0001c0001t0012g0123others(1): Show | 4 | HG03017.hp2 HG03492.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-968_474-961del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204531 | ||||||
chr2:127204531
|
AAGAAAGA others(5): Show |
A | 8 | a0001c0001t0002g0133a0001c0001t0002g0146a0001c0001t0002g0153others(5): Show | 9 | HG00733.hp2 HG00735.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.474-972_474-961del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204531 | ||||||
chr2:127204531
|
AAGAAAGA others(9): Show |
A | 2 | a0001c0001t0002g0115a0001c0001t0012g0330 | 2 | HG01261.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.474-976_474-961del others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204531 | ||||||
chr2:127204532
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.474-961T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204532 | ||||||
chr2:127204533
|
GAA | G | 12 | a0001c0001t0001g0189a0001c0001t0001g0192a0001c0001t0001g0235others(9): Show | 12 | HG01099.hp2 HG01109.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.474-964_474-963del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204533 | ||||||
chr2:127204535
|
A | G | 171 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0104others(168): Show | 176 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.474-964T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204535 | ||||||
chr2:127204535
|
AAG | A | 3 | a0001c0002t0004g0032a0001c0002t0004g0088a0001c0002t0007g0327 | 3 | HG01192.hp2 HG03453.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.474-966_474-965del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204535 | ||||||
chr2:127204537
|
G | GAA | 4 | a0001c0001t0001g0301a0001c0001t0003g0328a0001c0001t0008g0326others(1): Show | 4 | HG02922.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.474-967_474-966ins others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204537 | ||||||
chr2:127204539
|
G | A | 44 | a0001c0001t0001g0207a0001c0001t0001g0236a0001c0001t0001g0237others(41): Show | 44 | HG00639.hp2 HG01070.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.474-968C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204539 | ||||||
chr2:127204541
|
G | A | 1 | a0008c0015t0017g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.474-970C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204541 | ||||||
chr2:127204543
|
G | A | 24 | a0001c0001t0001g0144a0001c0001t0001g0236a0001c0001t0001g0340others(21): Show | 24 | HG01081.hp1 HG01516.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.474-972C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204543 | ||||||
chr2:127204545
|
G | A | 1 | a0008c0015t0017g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.474-974C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204545 | ||||||
chr2:127204545
|
GAGAGAGA others(15): Show |
G | 1 | a0001c0001t0048g0125 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.474-996_474-975del others(22): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204545 | ||||||
chr2:127204547
|
G | A | 25 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0169others(22): Show | 27 | HG00558.hp1 HG00738.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.474-976C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | ||||||
chr2:127204547
|
G | GAAGAAAG others(6): Show |
1 | a0001c0001t0001g0288 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.474-977_474-976ins others(13): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | ||||||
chr2:127204547
|
GAGAGAGA others(5): Show |
G | 1 | a0001c0001t0002g0114 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.474-988_474-977del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | ||||||
chr2:127204547
|
GAGAGAGA others(9): Show |
G | 3 | a0001c0001t0001g0131a0001c0001t0002g0129a0001c0002t0005g0130 | 3 | HG00438.hp1 NA18944.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.474-992_474-977del others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | ||||||
chr2:127204547
|
GAGAGAGA others(13): Show |
G | 2 | a0001c0001t0002g0151a0001c0001t0024g0150 | 2 | HG04204.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.474-996_474-977del others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | ||||||
chr2:127204547
|
GAGAGAGA others(17): Show |
G | 1 | a0001c0002t0007g0289 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.474-1000_474-977de others(25): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204547 | ||||||
chr2:127204549
|
GAGAGAGA others(3): Show |
G | 1 | a0001c0001t0002g0113 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.474-988_474-979del others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204549 | ||||||
chr2:127204551
|
G | A | 52 | a0001c0001t0001g0110a0001c0001t0001g0143a0001c0001t0001g0144others(49): Show | 55 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.474-980C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | ||||||
chr2:127204551
|
G | GAA | 5 | a0001c0001t0001g0030a0001c0001t0001g0204a0001c0001t0001g0293others(2): Show | 5 | HG00280.hp2 HG01952.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-981_474-980ins others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | ||||||
chr2:127204551
|
G | GAAAGAAA others(3): Show |
3 | a0001c0001t0001g0286a0001c0001t0003g0285a0002c0004t0020g0021 | 3 | HG03579.hp2 HG04204.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.474-981_474-980ins others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | ||||||
chr2:127204551
|
G | GAGAAAGA others(9): Show |
1 | a0002c0004t0020g0022 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.474-981_474-980ins others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | ||||||
chr2:127204551
|
G | GAGAGAGA others(15): Show |
1 | a0002c0003t0003g0024 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.474-981_474-980ins others(22): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | ||||||
chr2:127204551
|
G | GAGAGAGA others(17): Show |
1 | a0002c0003t0010g0017 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.474-981_474-980ins others(24): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | ||||||
chr2:127204551
|
GAGAGAGA others(5): Show |
G | 2 | a0001c0001t0002g0003a0001c0001t0002g0126 | 3 | HG02723.hp1 NA18951.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.474-992_474-981del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204551 | ||||||
chr2:127204553
|
GAGAGAAA others(15): Show |
G | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.474-1004_474-983de others(23): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204553 | ||||||
chr2:127204554
|
AG | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0261a0001c0002t0009g0035 | 3 | HG00558.hp2 HG02135.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.474-984delC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204554 | ||||||
chr2:127204555
|
G | A | 120 | a0001c0001t0001g0030a0001c0001t0001g0104a0001c0001t0001g0110others(117): Show | 123 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.474-984C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAA | 15 | a0001c0001t0001g0006a0001c0001t0001g0206a0001c0001t0001g0269others(12): Show | 17 | HG00408.hp1 HG01433.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.474-985_474-984ins others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAAAGAA | 3 | a0001c0001t0001g0071a0001c0001t0002g0231a0001c0002t0004g0070 | 3 | HG00609.hp1 HG02572.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.474-985_474-984ins others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAAAGA others(5): Show |
1 | a0001c0002t0006g0093 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.474-996_474-985dup others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAAAGA others(16): Show |
1 | a0002c0004t0019g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(23): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAAAGA others(15): Show |
1 | a0002c0003t0010g0023 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.474-985_474-984ins others(22): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAAGAA others(4): Show |
1 | a0001c0001t0002g0232 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAGAA | 3 | a0001c0001t0002g0102a0001c0001t0047g0038a0001c0002t0005g0039 | 3 | HG00423.hp1 HG02027.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.474-985_474-984ins others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAGAAA others(3): Show |
3 | a0001c0001t0001g0103a0001c0002t0005g0056a0001c0002t0005g0079 | 3 | HG02074.hp2 NA18961.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.474-985_474-984ins others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAGAAA others(7): Show |
1 | a0001c0002t0005g0080 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAGAAA others(15): Show |
1 | a0001c0002t0004g0098 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(22): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAGAAA others(19): Show |
1 | a0002c0003t0010g0019 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.474-985_474-984ins others(26): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAGAGA others(13): Show |
1 | a0001c0001t0002g0099 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.474-985_474-984ins others(20): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAGAGA others(21): Show |
2 | a0002c0003t0006g0027a0002c0003t0006g0028 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.474-985_474-984ins others(28): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
G | GAGAGAGA others(25): Show |
1 | a0002c0004t0020g0020 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.474-985_474-984ins others(32): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
GAGAA | G | 7 | a0001c0001t0001g0096a0001c0001t0008g0036a0001c0001t0013g0060others(4): Show | 7 | HG01123.hp1 HG01243.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.474-988_474-985del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
GAGAAAGA others(1): Show |
G | 4 | a0001c0001t0001g0046a0001c0001t0002g0176a0001c0001t0024g0152others(1): Show | 4 | HG02056.hp2 HG03710.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-992_474-985del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
GAGAAAGA others(5): Show |
G | 2 | a0001c0001t0002g0112a0001c0002t0009g0086 | 2 | HG01516.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.474-996_474-985del others(12): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
GAGAAAGA others(9): Show |
G | 1 | a0001c0002t0006g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.474-1000_474-985de others(17): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204555
|
GAGAAAGA others(13): Show |
G | 1 | a0001c0005t0002g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.474-1004_474-985de others(21): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204555 | ||||||
chr2:127204557
|
GA | G | 4 | a0001c0001t0001g0299a0001c0001t0034g0308a0001c0001t0050g0156others(1): Show | 4 | HG02683.hp2 HG03927.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-987delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | ||||||
chr2:127204557
|
GAA | G | 9 | a0001c0001t0001g0196a0001c0001t0001g0237a0001c0001t0001g0242others(6): Show | 9 | HG01884.hp2 HG01952.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.474-988_474-987del others(2): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | ||||||
chr2:127204557
|
GAAAGAA | G | 3 | a0001c0001t0001g0302a0001c0002t0005g0055a0001c0002t0007g0094 | 3 | HG03195.hp2 NA18980.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.474-992_474-987del others(6): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | ||||||
chr2:127204557
|
GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0001g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.474-996_474-987del others(10): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | ||||||
chr2:127204557
|
GAAAGAAA others(7): Show |
G | 1 | a0003c0010t0029g0011 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.474-1000_474-987de others(15): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204557 | ||||||
chr2:127204559
|
A | G | 50 | a0001c0001t0001g0192a0001c0001t0001g0197a0001c0001t0001g0207others(47): Show | 51 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.474-988T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204559 | ||||||
chr2:127204563
|
A | G | 22 | a0001c0001t0001g0096a0001c0001t0001g0196a0001c0001t0001g0207others(19): Show | 22 | HG01123.hp1 HG01884.hp2 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.474-992T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204563 | ||||||
chr2:127204566
|
A | G | 2 | a0001c0001t0001g0298a0001c0002t0014g0029 | 2 | NA18962.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.474-995T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204566 | ||||||
chr2:127204567
|
A | G | 8 | a0001c0001t0001g0207a0001c0001t0001g0236a0001c0001t0001g0237others(5): Show | 8 | HG02647.hp1 HG02738.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-996T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204567 | ||||||
chr2:127204571
|
A | G | 1 | a0001c0002t0004g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.474-1000T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204571 | ||||||
chr2:127204575
|
A | G | 7 | a0001c0002t0006g0089a0002c0003t0006g0026a0002c0003t0010g0018others(4): Show | 7 | HG02615.hp1 HG02630.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.474-1004T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204575 | ||||||
chr2:127204578
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.474-1007T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204578 | ||||||
chr2:127204579
|
A | G | 1 | a0001c0005t0002g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.474-1008T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204579 | ||||||
chr2:127204582
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.474-1011T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204582 | ||||||
chr2:127204591
|
A | C | 1 | a0001c0001t0002g0149 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.474-1020T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204591 | ||||||
chr2:127204594
|
A | C | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG02717.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.474-1023T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204594 | ||||||
chr2:127204598
|
A | C | 3 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0002t0009g0338 | 3 | HG02717.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.474-1027T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204598 | ||||||
chr2:127204602
|
A | AAAGCAAG others(5): Show |
1 | a0001c0001t0038g0339 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.474-1032_474-1031i others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204602 | ||||||
chr2:127204602
|
A | C | 3 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0002t0009g0338 | 3 | HG02717.hp2 HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.474-1031T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204602 | ||||||
chr2:127204606
|
A | C | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-1035T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204606 | ||||||
chr2:127204610
|
A | C | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.474-1039T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204610 | ||||||
chr2:127204614
|
A | AAAGAAAG others(5): Show |
1 | a0001c0001t0006g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.474-1044_474-1043i others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204614 | ||||||
chr2:127204619
|
A | C | 1 | a0001c0001t0001g0220 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.474-1048T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204619 | ||||||
chr2:127204622
|
AAAG | A | 34 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0207others(31): Show | 34 | HG00438.hp2 HG00738.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.474-1054_474-1052d others(5): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204622 | ||||||
chr2:127204623
|
A | C | 1 | a0001c0002t0007g0334 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.474-1052T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204623 | ||||||
chr2:127204625
|
G | GA | 114 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0104others(111): Show | 116 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.474-1055dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | ||||||
chr2:127204625
|
G | GAAAGA | 8 | a0001c0001t0001g0200a0001c0001t0001g0276a0001c0001t0001g0281others(5): Show | 8 | HG00609.hp2 HG00735.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.474-1055_474-1054i others(7): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | ||||||
chr2:127204625
|
G | GAAAGAAA others(2): Show |
6 | a0001c0001t0001g0184a0001c0001t0001g0203a0001c0001t0001g0275others(3): Show | 6 | HG01175.hp1 HG02004.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.474-1055_474-1054i others(11): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | ||||||
chr2:127204625
|
G | GAAAGAAA others(6): Show |
1 | a0001c0001t0002g0307 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.474-1055_474-1054i others(15): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | ||||||
chr2:127204625
|
G | GAAAGAAA others(10): Show |
3 | a0001c0001t0001g0284a0001c0002t0015g0342a0002c0004t0041g0025 | 3 | HG02630.hp2 HG03516.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.474-1055_474-1054i others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | ||||||
chr2:127204625
|
G | GAAAGAAA others(14): Show |
2 | a0002c0003t0006g0026a0002c0004t0019g0015 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.474-1055_474-1054i others(23): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | ||||||
chr2:127204625
|
G | GAAAGAAA others(18): Show |
1 | a0002c0003t0010g0018 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.474-1055_474-1054i others(27): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204625 | ||||||
chr2:127204626
|
A | AC | 13 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0222others(10): Show | 13 | HG01175.hp2 HG02148.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.474-1056_474-1055i others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204626 | ||||||
chr2:127204626
|
A | C | 5 | a0001c0001t0001g0220a0001c0001t0025g0221a0001c0001t0025g0306others(2): Show | 5 | HG01099.hp1 HG01891.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.474-1055T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204626 | ||||||
chr2:127204628
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.474-1057C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204628 | ||||||
chr2:127204629
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.474-1058T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204629 | ||||||
chr2:127204722
|
G | A | 2 | a0001c0001t0021g0320a0001c0001t0021g0321 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.474-1151C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204722 | ||||||
chr2:127204917
|
T | C | 271 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0104others(268): Show | 278 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.473+983A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127204917 | ||||||
chr2:127205059
|
A | G | 146 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0104others(143): Show | 148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.473+841T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205059 | ||||||
chr2:127205206
|
G | A | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+694C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205206 | ||||||
chr2:127205238
|
C | T | 2 | a0003c0008t0008g0007a0003c0008t0008g0008 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.473+662G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205238 | ||||||
chr2:127205282
|
C | A | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+618G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205282 | ||||||
chr2:127205344
|
G | A | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.473+556C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205344 | ||||||
chr2:127205345
|
G | A | 1 | a0001c0001t0002g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.473+555C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205345 | ||||||
chr2:127205428
|
T | G | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+472A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205428 | ||||||
chr2:127205520
|
G | A | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.473+380C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205520 | ||||||
chr2:127205578
|
G | A | 2 | a0001c0002t0004g0052a0001c0002t0004g0072 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.473+322C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205578 | ||||||
chr2:127205692
|
C | A | 10 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0220others(7): Show | 10 | HG01099.hp1 HG01928.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.473+208G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205692 | ||||||
chr2:127205847
|
TC | T | 146 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0104others(143): Show | 148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.473+52delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205847 | ||||||
chr2:127205897
|
C | T | 10 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.473+3G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 2/8 | chr2 | 127205897 | ||||||
chr2:127206159
|
C | G | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-69G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206159 | ||||||
chr2:127206192
|
A | C | 4 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-102T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206192 | ||||||
chr2:127206199
|
T | G | 7 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(4): Show | 7 | HG02717.hp2 HG02922.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-109A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206199 | ||||||
chr2:127206290
|
CGTTT | C | 244 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0110others(241): Show | 251 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.283-204_283-201del others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206290 | ||||||
chr2:127206290
|
CGTTTGTT others(1): Show |
C | 9 | a0001c0001t0001g0096a0001c0001t0001g0340a0001c0001t0001g0341others(6): Show | 9 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-208_283-201del others(8): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206290 | ||||||
chr2:127206295
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283-205C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206295 | ||||||
chr2:127206307
|
G | T | 1 | a0001c0002t0006g0092 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.283-217C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206307 | ||||||
chr2:127206308
|
T | C | 10 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.283-218A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206308 | ||||||
chr2:127206308
|
T | G | 1 | a0001c0002t0006g0092 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.283-218A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206308 | ||||||
chr2:127206427
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.283-337C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206427 | ||||||
chr2:127206452
|
G | T | 2 | a0001c0001t0002g0231a0001c0001t0002g0232 | 2 | NA19002.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.283-362C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206452 | ||||||
chr2:127206536
|
G | A | 1 | a0001c0001t0008g0054 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.283-446C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206536 | ||||||
chr2:127206749
|
C | T | 2 | a0001c0001t0001g0030a0001c0002t0009g0081 | 2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.283-659G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206749 | ||||||
chr2:127206973
|
A | G | 21 | a0001c0001t0001g0103a0001c0001t0002g0078a0001c0001t0002g0099others(18): Show | 21 | HG00423.hp1 HG01123.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.283-883T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127206973 | ||||||
chr2:127207048
|
T | A | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-958A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207048 | ||||||
chr2:127207056
|
C | G | 8 | a0002c0003t0003g0024a0002c0003t0006g0026a0002c0003t0006g0027others(5): Show | 8 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.283-966G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207056 | ||||||
chr2:127207145
|
G | A | 80 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(77): Show | 85 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.283-1055C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207145 | ||||||
chr2:127207296
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.283-1206T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207296 | ||||||
chr2:127207408
|
C | A | 1 | a0001c0001t0006g0073 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.283-1318G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207408 | ||||||
chr2:127207515
|
C | A | 5 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0147others(2): Show | 5 | HG00280.hp1 HG00733.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-1425G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207515 | ||||||
chr2:127207660
|
ACT | A | 15 | a0002c0003t0003g0024a0002c0003t0006g0026a0002c0003t0006g0027others(12): Show | 15 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.283-1572_283-1571d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207660 | ||||||
chr2:127207678
|
A | T | 87 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(84): Show | 92 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.283-1588T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207678 | ||||||
chr2:127207680
|
AT | A | 22 | a0001c0001t0001g0103a0001c0001t0001g0290a0001c0001t0002g0078others(19): Show | 22 | HG00423.hp1 HG01123.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.283-1591delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207680 | ||||||
chr2:127207681
|
T | A | 3 | a0001c0001t0003g0325a0001c0001t0008g0326a0001c0002t0001g0324 | 3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283-1591A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207681 | ||||||
chr2:127207818
|
A | G | 1 | a0008c0015t0017g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283-1728T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207818 | ||||||
chr2:127207912
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.283-1822T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127207912 | ||||||
chr2:127208167
|
C | A | 343 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0046others(340): Show | 350 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(347): Show |
intron_variant | MODIFIER | c.283-2077G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208167 | ||||||
chr2:127208184
|
C | A | 3 | a0001c0002t0009g0057a0001c0002t0009g0086a0001c0002t0042g0044 | 3 | HG01891.hp1 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.283-2094G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208184 | ||||||
chr2:127208235
|
A | C | 146 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0180others(143): Show | 148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.283-2145T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208235 | ||||||
chr2:127208269
|
A | G | 88 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(85): Show | 93 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.283-2179T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208269 | ||||||
chr2:127208295
|
C | T | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-2205G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208295 | ||||||
chr2:127208325
|
G | A | 1 | a0001c0002t0018g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-2235C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208325 | ||||||
chr2:127208389
|
C | T | 6 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(3): Show | 6 | HG02717.hp2 HG02922.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-2299G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208389 | ||||||
chr2:127208519
|
C | T | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-2429G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208519 | ||||||
chr2:127208680
|
C | A | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2590G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208680 | ||||||
chr2:127208722
|
A | C | 1 | a0001c0001t0003g0230 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.283-2632T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208722 | ||||||
chr2:127208863
|
T | G | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-2773A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208863 | ||||||
chr2:127208897
|
C | T | 2 | a0001c0001t0013g0106a0001c0001t0013g0111 | 2 | NA18957.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.283-2807G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208897 | ||||||
chr2:127208902
|
C | T | 1 | a0001c0002t0018g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-2812G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208902 | ||||||
chr2:127208917
|
CTT | C | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2829_283-2828d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127208917 | ||||||
chr2:127209049
|
G | A | 2 | a0001c0001t0001g0030a0001c0002t0009g0081 | 2 | HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.283-2959C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209049 | ||||||
chr2:127209061
|
T | C | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0003g0034 | 3 | HG02451.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.283-2971A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209061 | ||||||
chr2:127209116
|
C | T | 81 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(78): Show | 86 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.283-3026G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209116 | ||||||
chr2:127209160
|
T | C | 3 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339 | 3 | HG02717.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.283-3070A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209160 | ||||||
chr2:127209178
|
C | T | 1 | a0002c0003t0006g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.283-3088G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209178 | ||||||
chr2:127209375
|
G | C | 3 | a0001c0001t0003g0325a0001c0001t0008g0326a0001c0002t0001g0324 | 3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283-3285C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209375 | ||||||
chr2:127209492
|
A | G | 3 | a0001c0001t0002g0146a0001c0001t0002g0147a0001c0001t0002g0148 | 3 | HG01255.hp2 HG02486.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.283-3402T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209492 | ||||||
chr2:127209741
|
C | T | 1 | a0008c0015t0017g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.283-3651G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209741 | ||||||
chr2:127209838
|
C | T | 4 | a0001c0001t0003g0328a0001c0002t0015g0329a0001c0002t0015g0342others(1): Show | 4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-3748G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209838 | ||||||
chr2:127209887
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.283-3797G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127209887 | ||||||
chr2:127210042
|
T | A | 7 | a0002c0003t0010g0017a0002c0003t0010g0018a0002c0003t0010g0019others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-3952A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210042 | ||||||
chr2:127210266
|
T | G | 2 | a0001c0002t0018g0194a0001c0002t0018g0223 | 2 | HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.283-4176A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210266 | ||||||
chr2:127210358
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0002g0292 | 2 | HG00544.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.283-4268C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210358 | ||||||
chr2:127210432
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.283-4342T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210432 | ||||||
chr2:127210541
|
C | A | 1 | a0001c0001t0002g0307 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.283-4451G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210541 | ||||||
chr2:127210930
|
C | A | 6 | a0001c0001t0002g0058a0001c0001t0002g0084a0001c0002t0007g0059others(3): Show | 6 | HG00639.hp2 HG01081.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-4840G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127210930 | ||||||
chr2:127211081
|
G | A | 1 | a0001c0002t0007g0085 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.283-4991C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211081 | ||||||
chr2:127211088
|
A | G | 4 | a0001c0001t0003g0328a0001c0002t0015g0329a0001c0002t0015g0342others(1): Show | 4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-4998T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211088 | ||||||
chr2:127211127
|
G | A | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.283-5037C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211127 | ||||||
chr2:127211267
|
A | AACGACTC others(5): Show |
1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5178_283-5177i others(14): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211267 | ||||||
chr2:127211286
|
A | C | 81 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(78): Show | 86 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.283-5196T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211286 | ||||||
chr2:127211309
|
A | G | 7 | a0002c0003t0010g0017a0002c0003t0010g0018a0002c0003t0010g0019others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-5219T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211309 | ||||||
chr2:127211361
|
G | GTTTTTTT others(4): Show |
1 | a0002c0003t0003g0024 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.283-5272_283-5271i others(13): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | ||||||
chr2:127211361
|
GTTTTTTT others(6): Show |
G | 23 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(20): Show | 23 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.283-5284_283-5272d others(15): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | ||||||
chr2:127211361
|
GTTTTTTT others(7): Show |
G | 56 | a0001c0001t0001g0169a0001c0001t0002g0001a0001c0001t0002g0003others(53): Show | 61 | HG00280.hp2 HG00558.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.283-5285_283-5272d others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | ||||||
chr2:127211361
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0002g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.283-5286_283-5272d others(17): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | ||||||
chr2:127211361
|
GTTTTTTT others(9): Show |
G | 1 | a0001c0002t0016g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.283-5287_283-5272d others(18): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | ||||||
chr2:127211361
|
GTTTTTTT others(10): Show |
G | 2 | a0001c0002t0016g0332a0001c0002t0016g0333 | 2 | HG02257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.283-5288_283-5272d others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211361 | ||||||
chr2:127211363
|
T | A | 4 | a0001c0001t0003g0328a0001c0002t0015g0329a0001c0002t0015g0342others(1): Show | 4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-5273A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211363 | ||||||
chr2:127211369
|
G | GT | 24 | a0001c0001t0001g0046a0001c0001t0002g0058a0001c0001t0002g0099others(21): Show | 24 | HG00423.hp1 HG01081.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.283-5280dupA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | ||||||
chr2:127211369
|
G | T | 11 | a0001c0001t0005g0195a0001c0002t0005g0045a0001c0002t0018g0179others(8): Show | 11 | HG01123.hp1 HG01243.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.283-5279C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | ||||||
chr2:127211369
|
GT | G | 150 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0189others(147): Show | 152 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(149): Show |
intron_variant | MODIFIER | c.283-5280delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | ||||||
chr2:127211369
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0045g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283-5293_283-5280d others(16): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | ||||||
chr2:127211369
|
GTTTTTTT others(10): Show |
G | 6 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(3): Show | 6 | HG00735.hp2 HG01168.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-5296_283-5280d others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211369 | ||||||
chr2:127211370
|
T | G | 1 | a0001c0001t0005g0195 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.283-5280A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211370 | ||||||
chr2:127211376
|
T | TG | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-5287_283-5286i others(3): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211376 | ||||||
chr2:127211377
|
T | G | 6 | a0001c0001t0001g0096a0001c0001t0001g0293a0001c0001t0002g0185others(3): Show | 6 | HG00544.hp2 HG02040.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.283-5287A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211377 | ||||||
chr2:127211378
|
T | G | 1 | a0001c0002t0004g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.283-5288A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211378 | ||||||
chr2:127211380
|
T | G | 7 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0301others(4): Show | 7 | HG00408.hp2 HG00642.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-5290A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211380 | ||||||
chr2:127211381
|
T | G | 9 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-5291A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211381 | ||||||
chr2:127211382
|
T | G | 12 | a0001c0001t0001g0204a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | HG01069.hp2 HG01256.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.283-5292A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211382 | ||||||
chr2:127211383
|
T | G | 1 | a0001c0002t0006g0089 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.283-5293A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211383 | ||||||
chr2:127211384
|
T | G | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-5294A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211384 | ||||||
chr2:127211385
|
T | G | 16 | a0001c0001t0001g0228a0001c0001t0001g0313a0001c0001t0010g0190others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.283-5295A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211385 | ||||||
chr2:127211386
|
T | G | 137 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0188others(134): Show | 139 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.283-5296A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211386 | ||||||
chr2:127211387
|
T | G | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5297A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211387 | ||||||
chr2:127211389
|
T | G | 9 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-5299A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211389 | ||||||
chr2:127211391
|
T | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0313a0001c0001t0023g0208 | 3 | NA18978.hp2 NA19077.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.283-5301A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211391 | ||||||
chr2:127211392
|
T | G | 110 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0188others(107): Show | 111 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.283-5302A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211392 | ||||||
chr2:127211393
|
T | G | 9 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.283-5303A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211393 | ||||||
chr2:127211395
|
T | G | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5305A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211395 | ||||||
chr2:127211408
|
A | C | 4 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-5318T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211408 | ||||||
chr2:127211408
|
A | G | 1 | a0001c0002t0016g0331 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.283-5318T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211408 | ||||||
chr2:127211454
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.283-5364G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211454 | ||||||
chr2:127211465
|
C | T | 2 | a0001c0001t0002g0105a0001c0001t0045g0107 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.283-5375G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211465 | ||||||
chr2:127211484
|
G | C | 1 | a0001c0001t0003g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.283-5394C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211484 | ||||||
chr2:127211507
|
C | T | 3 | a0001c0002t0007g0327a0001c0002t0032g0323a0008c0015t0017g0344 | 3 | HG03453.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-5417G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211507 | ||||||
chr2:127211555
|
T | G | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5465A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211555 | ||||||
chr2:127211558
|
T | G | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5468A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211558 | ||||||
chr2:127211570
|
A | G | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-5480T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211570 | ||||||
chr2:127211593
|
G | GCCAGGAT others(8): Show |
1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.283-5518_283-5504d others(17): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211593 | ||||||
chr2:127211597
|
G | A | 81 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(78): Show | 86 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.283-5507C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211597 | ||||||
chr2:127211753
|
T | C | 1 | a0001c0012t0001g0090 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.283-5663A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211753 | ||||||
chr2:127211892
|
A | T | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5802T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211892 | ||||||
chr2:127211893
|
T | G | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-5803A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211893 | ||||||
chr2:127211913
|
T | C | 1 | a0001c0002t0018g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.283-5823A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127211913 | ||||||
chr2:127212095
|
A | T | 2 | a0001c0002t0032g0323a0008c0015t0017g0344 | 2 | HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-6005T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212095 | ||||||
chr2:127212098
|
C | A | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-6008G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212098 | ||||||
chr2:127212121
|
G | T | 4 | a0003c0006t0017g0010a0003c0006t0017g0012a0003c0008t0008g0007others(1): Show | 4 | HG02109.hp1 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-6031C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212121 | ||||||
chr2:127212186
|
A | G | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-6096T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212186 | ||||||
chr2:127212210
|
T | C | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-6120A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212210 | ||||||
chr2:127212236
|
A | C | 146 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0180others(143): Show | 148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.283-6146T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212236 | ||||||
chr2:127212300
|
C | G | 1 | a0001c0002t0001g0324 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283-6210G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212300 | ||||||
chr2:127212512
|
A | C | 4 | a0001c0001t0003g0325a0001c0001t0008g0326a0001c0002t0001g0324others(1): Show | 4 | HG01884.hp2 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-6422T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212512 | ||||||
chr2:127212529
|
C | T | 1 | a0001c0001t0001g0211 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.283-6439G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212529 | ||||||
chr2:127212580
|
A | G | 2 | a0001c0001t0002g0126a0001c0001t0002g0127 | 2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.283-6490T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212580 | ||||||
chr2:127212695
|
C | A | 1 | a0001c0001t0003g0319 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.283-6605G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212695 | ||||||
chr2:127212809
|
T | C | 251 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0110others(248): Show | 258 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.283-6719A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212809 | ||||||
chr2:127212873
|
A | T | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.283-6783T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212873 | ||||||
chr2:127212888
|
C | T | 1 | a0001c0001t0001g0210 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.283-6798G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212888 | ||||||
chr2:127212902
|
T | G | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-6812A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212902 | ||||||
chr2:127212933
|
A | C | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-6843T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212933 | ||||||
chr2:127212999
|
C | T | 1 | a0001c0002t0022g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.283-6909G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127212999 | ||||||
chr2:127213068
|
T | G | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+6921A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213068 | ||||||
chr2:127213083
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+6906A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213083 | ||||||
chr2:127213086
|
A | T | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+6903T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213086 | ||||||
chr2:127213143
|
A | C | 81 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(78): Show | 86 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.282+6846T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213143 | ||||||
chr2:127213164
|
G | T | 1 | a0001c0001t0048g0125 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.282+6825C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213164 | ||||||
chr2:127213166
|
G | A | 7 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0298others(4): Show | 7 | NA18947.hp1 NA18950.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+6823C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213166 | ||||||
chr2:127213292
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+6697A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213292 | ||||||
chr2:127213307
|
G | GA | 180 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0180others(177): Show | 182 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.282+6681dupT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213307 | ||||||
chr2:127213318
|
A | AC | 78 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(75): Show | 83 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.282+6670dupG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213318 | ||||||
chr2:127213318
|
A | C | 2 | a0001c0001t0002g0124a0001c0001t0012g0123 | 2 | NA18947.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.282+6671T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213318 | ||||||
chr2:127213585
|
T | C | 8 | a0002c0003t0003g0024a0002c0003t0006g0026a0002c0003t0006g0027others(5): Show | 8 | HG01243.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.282+6404A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213585 | ||||||
chr2:127213606
|
T | C | 5 | a0001c0002t0006g0042a0001c0002t0006g0091a0001c0002t0006g0092others(2): Show | 5 | HG02015.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+6383A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213606 | ||||||
chr2:127213649
|
T | A | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+6340A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213649 | ||||||
chr2:127213699
|
G | A | 8 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(5): Show | 8 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+6290C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213699 | ||||||
chr2:127213704
|
A | C | 1 | a0001c0002t0042g0044 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.282+6285T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213704 | ||||||
chr2:127213724
|
C | T | 1 | a0002c0004t0019g0014 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.282+6265G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213724 | ||||||
chr2:127213963
|
A | G | 19 | a0001c0001t0001g0110a0001c0001t0002g0105a0001c0001t0002g0109others(16): Show | 19 | HG00423.hp2 HG00733.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.282+6026T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127213963 | ||||||
chr2:127214014
|
C | T | 2 | a0001c0001t0023g0208a0001c0001t0023g0209 | 2 | HG02015.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.282+5975G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214014 | ||||||
chr2:127214125
|
A | T | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+5864T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214125 | ||||||
chr2:127214126
|
C | A | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+5863G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214126 | ||||||
chr2:127214162
|
G | C | 146 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0180others(143): Show | 148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.282+5827C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214162 | ||||||
chr2:127214217
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.282+5772C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214217 | ||||||
chr2:127214237
|
A | C | 252 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0110others(249): Show | 259 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.282+5752T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214237 | ||||||
chr2:127214358
|
A | T | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+5631T>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214358 | ||||||
chr2:127214386
|
G | A | 9 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+5603C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214386 | ||||||
chr2:127214467
|
C | G | 1 | a0001c0001t0003g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.282+5522G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214467 | ||||||
chr2:127214542
|
A | C | 4 | a0001c0001t0003g0328a0001c0002t0015g0329a0001c0002t0015g0342others(1): Show | 4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+5447T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214542 | ||||||
chr2:127214652
|
T | C | 146 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0180others(143): Show | 148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.282+5337A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214652 | ||||||
chr2:127214678
|
T | G | 36 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0003g0328others(33): Show | 36 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.282+5311A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214678 | ||||||
chr2:127214736
|
C | T | 107 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(104): Show | 112 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.282+5253G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214736 | ||||||
chr2:127214780
|
T | C | 1 | a0001c0002t0018g0179 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.282+5209A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214780 | ||||||
chr2:127214782
|
G | GT | 35 | a0001c0001t0001g0104a0001c0001t0001g0189a0001c0001t0001g0192others(32): Show | 35 | HG00423.hp1 HG00609.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.282+5206dupA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214782 | ||||||
chr2:127214782
|
G | T | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+5207C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214782 | ||||||
chr2:127214782
|
GT | G | 16 | a0001c0001t0002g0105a0001c0001t0003g0328a0001c0002t0007g0334others(13): Show | 16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.282+5206delA | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214782 | ||||||
chr2:127214788
|
T | G | 4 | a0001c0001t0001g0096a0001c0002t0007g0094a0004c0007t0026g0097others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+5201A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214788 | ||||||
chr2:127214789
|
T | G | 83 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(80): Show | 88 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.282+5200A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214789 | ||||||
chr2:127214790
|
T | G | 12 | a0001c0001t0002g0105a0001c0002t0007g0334a0001c0002t0007g0335others(9): Show | 12 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.282+5199A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214790 | ||||||
chr2:127214798
|
TTG | T | 82 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(79): Show | 87 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.282+5189_282+5190d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214798 | ||||||
chr2:127214799
|
T | G | 1 | a0001c0001t0013g0106 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.282+5190A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214799 | ||||||
chr2:127214800
|
G | T | 5 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(2): Show | 5 | HG02647.hp2 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+5189C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214800 | ||||||
chr2:127214801
|
G | T | 2 | a0001c0001t0001g0188a0001c0001t0003g0187 | 2 | HG02135.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.282+5188C>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214801 | ||||||
chr2:127214802
|
T | G | 87 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(84): Show | 92 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.282+5187A>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214802 | ||||||
chr2:127214851
|
G | A | 3 | a0001c0001t0001g0096a0004c0007t0026g0097a0004c0007t0027g0095 | 3 | HG02451.hp1 HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.282+5138C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214851 | ||||||
chr2:127214866
|
C | T | 269 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0110others(266): Show | 276 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.282+5123G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127214866 | ||||||
chr2:127215019
|
C | T | 4 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+4970G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215019 | ||||||
chr2:127215128
|
CA | C | 8 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(5): Show | 8 | HG02109.hp1 HG02717.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+4860delT | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215128 | ||||||
chr2:127215128
|
CAA | C | 262 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0110others(259): Show | 269 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.282+4859_282+4860d others(4): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215128 | ||||||
chr2:127215131
|
A | C | 1 | a0001c0002t0004g0033 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.282+4858T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215131 | ||||||
chr2:127215197
|
T | C | 2 | a0001c0001t0002g0307a0001c0001t0002g0311 | 2 | HG02155.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.282+4792A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215197 | ||||||
chr2:127215243
|
T | A | 9 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+4746A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215243 | ||||||
chr2:127215290
|
T | A | 2 | a0001c0001t0002g0178a0001c0001t0044g0177 | 2 | HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.282+4699A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215290 | ||||||
chr2:127215383
|
G | C | 9 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+4606C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215383 | ||||||
chr2:127215589
|
G | C | 1 | a0001c0001t0001g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.282+4400C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215589 | ||||||
chr2:127215627
|
T | C | 3 | a0001c0001t0003g0325a0001c0001t0008g0326a0001c0002t0001g0324 | 3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+4362A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215627 | ||||||
chr2:127215739
|
G | A | 1 | a0001c0001t0034g0308 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.282+4250C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215739 | ||||||
chr2:127215779
|
A | G | 1 | a0001c0002t0004g0032 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.282+4210T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215779 | ||||||
chr2:127215783
|
G | A | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+4206C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127215783 | ||||||
chr2:127216044
|
T | C | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+3945A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216044 | ||||||
chr2:127216267
|
C | T | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+3722G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216267 | ||||||
chr2:127216329
|
T | TATAGTCA others(10): Show |
1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+3659_282+3660i others(19): Show |
CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216329 | ||||||
chr2:127216345
|
A | C | 1 | a0001c0005t0002g0031 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.282+3644T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216345 | ||||||
chr2:127216529
|
G | A | 4 | a0001c0001t0003g0328a0001c0002t0015g0329a0001c0002t0015g0342others(1): Show | 4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+3460C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216529 | ||||||
chr2:127216626
|
G | A | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+3363C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216626 | ||||||
chr2:127216792
|
A | G | 1 | a0001c0001t0012g0186 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282+3197T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127216792 | ||||||
chr2:127217299
|
T | C | 10 | a0001c0002t0007g0334a0001c0002t0007g0335a0001c0002t0007g0336others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.282+2690A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217299 | ||||||
chr2:127217361
|
T | C | 145 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0180others(142): Show | 147 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+2628A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217361 | ||||||
chr2:127217369
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.282+2620C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217369 | ||||||
chr2:127217393
|
T | C | 4 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0038g0339others(1): Show | 4 | HG02717.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.282+2596A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217393 | ||||||
chr2:127217487
|
C | T | 2 | a0001c0001t0021g0320a0001c0001t0021g0321 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.282+2502G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217487 | ||||||
chr2:127217548
|
T | C | 1 | a0001c0001t0001g0309 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.282+2441A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217548 | ||||||
chr2:127217559
|
C | G | 1 | a0001c0001t0002g0185 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.282+2430G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217559 | ||||||
chr2:127217927
|
T | A | 6 | a0003c0006t0017g0010a0003c0006t0017g0012a0003c0006t0028g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+2062A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217927 | ||||||
chr2:127217960
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.282+2029C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217960 | ||||||
chr2:127217996
|
T | C | 1 | a0001c0001t0002g0311 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.282+1993A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127217996 | ||||||
chr2:127218045
|
C | A | 98 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0137others(95): Show | 102 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.282+1944G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218045 | ||||||
chr2:127218066
|
T | C | 1 | a0001c0002t0004g0098 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.282+1923A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218066 | ||||||
chr2:127218150
|
T | A | 1 | a0001c0001t0001g0312 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.282+1839A>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218150 | ||||||
chr2:127218162
|
C | T | 4 | a0001c0001t0003g0328a0001c0002t0015g0329a0001c0002t0015g0342others(1): Show | 4 | HG02258.hp2 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+1827G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218162 | ||||||
chr2:127218403
|
TC | T | 6 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0183others(3): Show | 6 | HG00735.hp2 HG01168.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+1585delG | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218403 | ||||||
chr2:127218463
|
T | TG | 6 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0002g0099others(3): Show | 6 | HG01928.hp2 HG02738.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+1525dupC | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218463 | ||||||
chr2:127218562
|
C | A | 2 | a0001c0001t0001g0103a0001c0001t0002g0102 | 2 | NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.282+1427G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218562 | ||||||
chr2:127218625
|
C | T | 2 | a0003c0008t0008g0007a0003c0008t0008g0008 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.282+1364G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218625 | ||||||
chr2:127218798
|
A | C | 268 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0110others(265): Show | 275 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.282+1191T>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127218798 | ||||||
chr2:127219241
|
C | G | 145 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0180others(142): Show | 147 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.282+748G>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219241 | ||||||
chr2:127219384
|
C | T | 1 | a0001c0002t0007g0327 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+605G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219384 | ||||||
chr2:127219475
|
A | G | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.282+514T>C | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219475 | ||||||
chr2:127219491
|
C | A | 1 | a0008c0015t0017g0344 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.282+498G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219491 | ||||||
chr2:127219542
|
T | C | 269 | a0001c0001t0001g0006a0001c0001t0001g0104a0001c0001t0001g0110others(266): Show | 276 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.282+447A>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219542 | ||||||
chr2:127219595
|
C | A | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+394G>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219595 | ||||||
chr2:127219707
|
C | T | 6 | a0003c0006t0017g0010a0003c0006t0017g0012a0003c0006t0028g0009others(3): Show | 6 | HG02109.hp1 HG02647.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+282G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219707 | ||||||
chr2:127219740
|
C | T | 3 | a0001c0001t0003g0325a0001c0001t0008g0326a0001c0002t0001g0324 | 3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.282+249G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219740 | ||||||
chr2:127219791
|
C | T | 1 | a0001c0002t0032g0323 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.282+198G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219791 | ||||||
chr2:127219858
|
G | A | 5 | a0001c0001t0003g0315a0001c0001t0003g0316a0001c0001t0003g0317others(2): Show | 5 | HG01081.hp2 HG01934.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+131C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219858 | ||||||
chr2:127219860
|
G | A | 2 | a0001c0001t0021g0320a0001c0001t0021g0321 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.282+129C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219860 | ||||||
chr2:127219868
|
G | A | 1 | a0001c0001t0001g0322 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.282+121C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219868 | ||||||
chr2:127219871
|
C | T | 1 | a0001c0002t0014g0029 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.282+118G>A | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219871 | ||||||
chr2:127219974
|
G | A | 21 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0003g0325others(18): Show | 21 | HG01175.hp2 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.282+15C>T | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219974 | ||||||
chr2:127219974
|
G | C | 153 | a0001c0001t0001g0006a0001c0001t0001g0180a0001c0001t0001g0181others(150): Show | 155 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.282+15C>G | CYP27C1 | ENSG00000186684.14 | transcript | ENST00000664447.2 | protein_coding | 1/8 | chr2 | 127219974 |