geneid | 55556 |
---|---|
ensemblid | ENSG00000132199.20 |
hgncid | 30365 |
symbol | ENOSF1 |
name | enolase superfamily member 1 |
refseq_nuc | NM_017512.7 |
refseq_prot | NP_059982.2 |
ensembl_nuc | ENST00000647584.2 |
ensembl_prot | ENSP00000497230.2 |
mane_status | MANE Select |
chr | chr18 |
start | 670318 |
end | 712630 |
strand | - |
ver | v1.2 |
region | chr18:670318-712630 |
region5000 | chr18:665318-717630 |
regionname0 | ENOSF1_chr18_670318_712630 |
regionname5000 | ENOSF1_chr18_665318_717630 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 443 | 267 | 60 | 43 | 119 | 10 | 34 | 96 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002 | 0/1 | 443 | 82 | 24 | 26 | 17 | 3 | 11 | 10 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003 | 0/0 | 443 | 54 | 1 | 3 | 46 | 1 | 3 | 32 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0004 | 0/0 | 443 | 7 | 0 | 4 | 0 | 3 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0005 | 0/0 | 195 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0006 | 0/0 | 443 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0007 | 0/0 | 443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0008 | 0/0 | 443 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0009 | 0/0 | 443 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0010 | 0/0 | 443 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1332 | 212 | 45 | 41 | 83 | 10 | 32 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0002 | 0/1 | 1332 | 64 | 23 | 12 | 16 | 2 | 10 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0003 | 0/0 | 1332 | 41 | 3 | 2 | 34 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0004 | 0/0 | 1332 | 39 | 0 | 3 | 35 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0005 | 0/0 | 1332 | 17 | 0 | 14 | 1 | 1 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0006 | 0/0 | 1332 | 12 | 12 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0007 | 0/0 | 1332 | 12 | 1 | 0 | 10 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0008 | 0/0 | 1332 | 7 | 0 | 4 | 0 | 3 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0009 | 0/0 | 991 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0010 | 0/0 | 1332 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0011 | 0/0 | 1332 | 2 | 0 | 0 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0012 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0013 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0014 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0015 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0016 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0017 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0018 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
c0019 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 4031 | 122 | 11 | 41 | 40 | 10 | 19 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0002 | 0/0 | 4019 | 121 | 20 | 12 | 69 | 2 | 18 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0003 | 0/0 | 4019 | 36 | 0 | 1 | 34 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0004 | 0/0 | 4019 | 34 | 12 | 3 | 14 | 2 | 3 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0005 | 0/1 | 4032 | 16 | 2 | 7 | 0 | 2 | 4 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0006 | 0/0 | 4019 | 10 | 10 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0007 | 0/0 | 4032 | 8 | 1 | 0 | 7 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0008 | 0/0 | 4031 | 8 | 0 | 0 | 8 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0009 | 0/0 | 4033 | 6 | 6 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0010 | 0/0 | 4031 | 6 | 0 | 5 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0011 | 0/0 | 4031 | 6 | 6 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0012 | 0/0 | 4019 | 6 | 5 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0013 | 0/0 | 4031 | 5 | 5 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0014 | 0/0 | 4033 | 2 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0015 | 0/0 | 4022 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0016 | 0/0 | 4019 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0017 | 0/0 | 4019 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0018 | 0/0 | 4019 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0019 | 0/0 | 4019 | 2 | 0 | 1 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0020 | 0/0 | 4019 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0021 | 0/0 | 4019 | 2 | 1 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0022 | 0/0 | 4031 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0023 | 0/0 | 4032 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0024 | 0/0 | 4032 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0025 | 0/0 | 4032 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0026 | 0/0 | 4031 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0027 | 0/0 | 4032 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0028 | 0/0 | 4031 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0029 | 0/0 | 4031 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0030 | 0/0 | 4078 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0031 | 0/0 | 4031 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0032 | 0/0 | 4022 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0033 | 0/0 | 4022 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0034 | 0/0 | 4028 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0035 | 0/0 | 4019 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0036 | 0/0 | 4045 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0037 | 0/0 | 4020 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0038 | 0/0 | 4019 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
t0039 | 0/0 | 4019 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0003 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0397 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
g0402 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1332 | 212 | 45 | 41 | 83 | 10 | 32 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0003 | 0/0 | 1332 | 41 | 3 | 2 | 34 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0006 | 0/0 | 1332 | 12 | 12 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0013 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0017 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002 | 0/1 | 1332 | 64 | 23 | 12 | 16 | 2 | 10 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0005 | 0/0 | 1332 | 17 | 0 | 14 | 1 | 1 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0015 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0004 | 0/0 | 1332 | 39 | 0 | 3 | 35 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0007 | 0/0 | 1332 | 12 | 1 | 0 | 10 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0011 | 0/0 | 1332 | 2 | 0 | 0 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0018 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0004c0008 | 0/0 | 1332 | 7 | 0 | 4 | 0 | 3 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0005c0009 | 0/0 | 991 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0006c0010 | 0/0 | 1332 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0007c0019 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0008c0016 | 0/0 | 1332 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0009c0014 | 0/0 | 1332 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0010c0012 | 0/0 | 1332 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5362 | 62 | 8 | 22 | 10 | 8 | 13 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0002 | 0/0 | 5350 | 102 | 17 | 10 | 57 | 1 | 17 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0006 | 0/0 | 5350 | 9 | 9 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0007 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0008 | 0/0 | 5362 | 8 | 0 | 0 | 8 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0010 | 0/0 | 5362 | 5 | 0 | 5 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0012 | 0/0 | 5350 | 6 | 5 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0014 | 0/0 | 5364 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0016 | 0/0 | 5350 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0017 | 0/0 | 5350 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0018 | 0/0 | 5350 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0019 | 0/0 | 5350 | 2 | 0 | 1 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0020 | 0/0 | 5350 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0022 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0028 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0032 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0034 | 0/0 | 5359 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0035 | 0/0 | 5350 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0037 | 0/0 | 5351 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0038 | 0/0 | 5350 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0001t0039 | 0/0 | 5350 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0003t0001 | 0/0 | 5362 | 32 | 3 | 2 | 25 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0003t0007 | 0/0 | 5363 | 6 | 0 | 0 | 6 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0003t0023 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0003t0026 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0003t0030 | 0/0 | 5409 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0006t0004 | 0/0 | 5350 | 12 | 12 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0013t0002 | 0/0 | 5350 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0001c0017t0001 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0001 | 0/0 | 5362 | 2 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0002 | 0/0 | 5350 | 4 | 0 | 1 | 2 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0004 | 0/0 | 5350 | 17 | 0 | 1 | 13 | 0 | 3 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0005 | 0/1 | 5363 | 16 | 2 | 7 | 0 | 2 | 4 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0006 | 0/0 | 5350 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0009 | 0/0 | 5364 | 6 | 6 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0011 | 0/0 | 5362 | 6 | 6 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0013 | 0/0 | 5362 | 5 | 5 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0014 | 0/0 | 5364 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0021 | 0/0 | 5350 | 2 | 1 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0024 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0025 | 0/0 | 5363 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0031 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0002t0033 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0005t0001 | 0/0 | 5362 | 17 | 0 | 14 | 1 | 1 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0002c0015t0002 | 0/0 | 5350 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0004t0001 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0004t0002 | 0/0 | 5350 | 2 | 0 | 1 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0004t0003 | 0/0 | 5350 | 33 | 0 | 1 | 31 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0004t0004 | 0/0 | 5350 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0004t0015 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0004t0036 | 0/0 | 5376 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0007t0002 | 0/0 | 5350 | 8 | 1 | 0 | 7 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0007t0003 | 0/0 | 5350 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0007t0010 | 0/0 | 5362 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0007t0015 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0011t0001 | 0/0 | 5362 | 2 | 0 | 0 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0003c0018t0007 | 0/0 | 5363 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0004c0008t0001 | 0/0 | 5362 | 3 | 0 | 2 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0004c0008t0004 | 0/0 | 5350 | 4 | 0 | 2 | 0 | 2 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0005c0009t0001 | 0/0 | 5021 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0006c0010t0002 | 0/0 | 5350 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0006c0010t0029 | 0/0 | 5362 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0007c0019t0003 | 0/0 | 5350 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0008c0016t0002 | 0/0 | 5350 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0009c0014t0027 | 0/0 | 5363 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
a0010c0012t0002 | 0/0 | 5350 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | copy fasta | chr18 | 665318 | 717630 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0270 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0001 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0008g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0008g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0008g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0008g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0010g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0012g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0014g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0016g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0016g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0017g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0017g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0018g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0018g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0019g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0019g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0020g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0020g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0022g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0028g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0032g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0034g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0035g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0037g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0038g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0001t0039g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0007g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0007g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0007g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0023g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0026g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0003t0030g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0006t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0013t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0001c0017t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0003 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0005g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0011g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0011g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0013g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0013g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0014g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0021g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0024g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0025g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0031g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0002t0033g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0005t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0002c0015t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0001g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0002g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0003g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0004g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0015g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0004t0036g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0002g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0003g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0010g0397 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0007t0015g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0011t0001g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0011t0001g0402 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0003c0018t0007g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0001g0386 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0004g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0004g0381 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0004c0008t0004g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0005c0009t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0005c0009t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0006c0010t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0006c0010t0029g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0007c0019t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0008c0016t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0009c0014t0027g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
a0010c0012t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0272 | EUR | GBR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | GBR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | GBR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00140 | hp2 | a0003 | c0007 | t0010 | g0397 | EUR | GBR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00280 | hp1 | a0002 | c0005 | t0001 | g0158 | EUR | FIN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0329 | EUR | FIN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00323 | hp1 | a0001 | c0001 | t0019 | g0161 | EUR | FIN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00323 | hp2 | a0010 | c0012 | t0002 | g0169 | EUR | FIN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00408 | hp2 | a0002 | c0002 | t0004 | g0211 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00423 | hp1 | a0003 | c0004 | t0003 | g0351 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0266 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00438 | hp2 | a0003 | c0004 | t0003 | g0396 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00544 | hp2 | a0003 | c0018 | t0007 | g0390 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00609 | hp1 | a0003 | c0007 | t0002 | g0379 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00621 | hp1 | a0002 | c0002 | t0004 | g0144 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00621 | hp2 | a0003 | c0004 | t0003 | g0359 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00642 | hp2 | a0002 | c0005 | t0001 | g0095 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0241 | EAS | CHS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0284 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG00741 | hp2 | a0001 | c0001 | t0010 | g0257 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01069 | hp1 | a0002 | c0002 | t0005 | g0179 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01069 | hp2 | a0001 | c0001 | t0010 | g0317 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01070 | hp1 | a0001 | c0001 | t0010 | g0224 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01070 | hp2 | a0002 | c0005 | t0001 | g0159 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0223 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01071 | hp2 | a0002 | c0002 | t0005 | g0178 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01074 | hp2 | a0004 | c0008 | t0004 | g0381 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01081 | hp2 | a0002 | c0005 | t0001 | g0063 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01106 | hp1 | a0002 | c0002 | t0005 | g0212 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01109 | hp1 | a0001 | c0001 | t0012 | g0192 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01109 | hp2 | a0001 | c0001 | t0039 | g0312 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01167 | hp1 | a0002 | c0002 | t0021 | g0182 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01175 | hp1 | a0003 | c0004 | t0002 | g0395 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01175 | hp2 | a0002 | c0005 | t0001 | g0094 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01192 | hp1 | a0002 | c0002 | t0025 | g0102 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01192 | hp2 | a0001 | c0001 | t0014 | g0300 | AMR | PUR | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01256 | hp1 | a0002 | c0002 | t0005 | g0134 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01257 | hp1 | a0002 | c0005 | t0001 | g0005 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01257 | hp2 | a0004 | c0008 | t0001 | g0367 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01258 | hp1 | a0004 | c0008 | t0001 | g0368 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01261 | hp2 | a0003 | c0004 | t0036 | g0364 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01346 | hp2 | a0001 | c0001 | t0010 | g0318 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01361 | hp1 | a0002 | c0005 | t0001 | g0038 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01433 | hp1 | a0002 | c0002 | t0005 | g0132 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01433 | hp2 | a0002 | c0002 | t0005 | g0003 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01496 | hp1 | a0002 | c0002 | t0005 | g0177 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01496 | hp2 | a0002 | c0002 | t0004 | g0181 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01515 | hp2 | a0002 | c0002 | t0005 | g0289 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01516 | hp1 | a0004 | c0008 | t0004 | g0011 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01517 | hp1 | a0002 | c0002 | t0005 | g0290 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01517 | hp2 | a0004 | c0008 | t0004 | g0011 | EUR | IBS | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01884 | hp1 | a0002 | c0002 | t0011 | g0104 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01884 | hp2 | a0001 | c0006 | t0004 | g0298 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01891 | hp1 | a0001 | c0006 | t0004 | g0235 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0060 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01928 | hp1 | a0002 | c0005 | t0001 | g0209 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0099 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01934 | hp1 | a0002 | c0005 | t0001 | g0176 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01943 | hp2 | a0002 | c0005 | t0001 | g0019 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01978 | hp2 | a0002 | c0005 | t0001 | g0136 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01993 | hp1 | a0004 | c0008 | t0004 | g0398 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02004 | hp1 | a0003 | c0004 | t0003 | g0387 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02004 | hp2 | a0002 | c0005 | t0001 | g0005 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0249 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0253 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0214 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02055 | hp2 | a0002 | c0002 | t0009 | g0026 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02056 | hp1 | a0002 | c0005 | t0001 | g0145 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02071 | hp1 | a0002 | c0002 | t0004 | g0140 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02080 | hp2 | a0002 | c0002 | t0004 | g0113 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02083 | hp1 | a0003 | c0004 | t0003 | g0013 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0293 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02132 | hp2 | a0003 | c0004 | t0004 | g0357 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02135 | hp1 | a0003 | c0004 | t0003 | g0347 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02148 | hp1 | a0002 | c0005 | t0001 | g0210 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02155 | hp1 | a0003 | c0004 | t0003 | g0400 | EAS | CDX | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02155 | hp2 | a0002 | c0002 | t0004 | g0137 | EAS | CDX | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CDX | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02165 | hp2 | a0003 | c0004 | t0003 | g0013 | EAS | CDX | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02257 | hp1 | a0009 | c0014 | t0027 | g0156 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0330 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02258 | hp1 | a0002 | c0002 | t0009 | g0089 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0231 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02300 | hp1 | a0002 | c0005 | t0001 | g0232 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02451 | hp1 | a0001 | c0006 | t0004 | g0002 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02523 | hp2 | a0003 | c0004 | t0003 | g0374 | EAS | KHV | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02572 | hp2 | a0001 | c0006 | t0004 | g0148 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02602 | hp2 | a0002 | c0002 | t0005 | g0097 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02615 | hp1 | a0002 | c0002 | t0009 | g0090 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0336 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02622 | hp1 | a0001 | c0001 | t0020 | g0236 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02630 | hp2 | a0001 | c0006 | t0004 | g0213 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02647 | hp1 | a0001 | c0006 | t0004 | g0002 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0153 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02683 | hp1 | a0003 | c0011 | t0001 | g0401 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02683 | hp2 | a0002 | c0002 | t0005 | g0175 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02717 | hp1 | a0001 | c0001 | t0034 | g0105 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02738 | hp2 | a0002 | c0002 | t0014 | g0096 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02809 | hp1 | a0002 | c0002 | t0013 | g0174 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02809 | hp2 | a0002 | c0002 | t0011 | g0103 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02818 | hp1 | a0002 | c0002 | t0024 | g0061 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02886 | hp1 | a0002 | c0002 | t0009 | g0133 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02886 | hp2 | a0001 | c0001 | t0038 | g0335 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02895 | hp1 | a0002 | c0002 | t0009 | g0131 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02895 | hp2 | a0003 | c0007 | t0002 | g0353 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0321 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02922 | hp1 | a0001 | c0006 | t0004 | g0006 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02976 | hp1 | a0002 | c0002 | t0031 | g0337 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02976 | hp2 | a0002 | c0002 | t0021 | g0184 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03041 | hp2 | a0002 | c0002 | t0013 | g0296 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03130 | hp1 | a0001 | c0006 | t0004 | g0149 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03130 | hp2 | a0001 | c0006 | t0004 | g0237 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03139 | hp1 | a0002 | c0002 | t0013 | g0018 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0207 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03195 | hp1 | a0001 | c0006 | t0004 | g0006 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03209 | hp1 | a0002 | c0002 | t0011 | g0299 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03209 | hp2 | a0001 | c0001 | t0012 | g0106 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03225 | hp1 | a0001 | c0001 | t0020 | g0191 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0170 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03453 | hp1 | a0002 | c0002 | t0011 | g0151 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03453 | hp2 | a0001 | c0001 | t0012 | g0059 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03486 | hp1 | a0002 | c0002 | t0009 | g0093 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03516 | hp2 | a0001 | c0001 | t0012 | g0041 | AFR | ESN | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03540 | hp1 | a0006 | c0010 | t0029 | g0345 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03540 | hp2 | a0002 | c0002 | t0011 | g0240 | AFR | GWD | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03579 | hp1 | a0001 | c0006 | t0004 | g0002 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03654 | hp1 | a0001 | c0003 | t0001 | g0341 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0279 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03704 | hp1 | a0002 | c0005 | t0001 | g0064 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03710 | hp2 | a0003 | c0004 | t0003 | g0371 | SAS | PJL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03831 | hp1 | a0002 | c0002 | t0005 | g0135 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03831 | hp2 | a0002 | c0002 | t0004 | g0183 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03834 | hp1 | a0003 | c0011 | t0001 | g0402 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03927 | hp1 | a0001 | c0001 | t0037 | g0128 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04115 | hp1 | a0002 | c0002 | t0004 | g0024 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04115 | hp2 | a0001 | c0001 | t0028 | g0304 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04184 | hp2 | a0002 | c0002 | t0004 | g0233 | SAS | BEB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | STU | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18522 | hp1 | a0002 | c0002 | t0013 | g0130 | AFR | YRI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | YRI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18612 | hp1 | a0003 | c0004 | t0003 | g0385 | EAS | CHB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18747 | hp1 | a0003 | c0004 | t0003 | g0377 | EAS | CHB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18747 | hp2 | a0003 | c0004 | t0003 | g0375 | EAS | CHB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18939 | hp1 | a0001 | c0003 | t0007 | g0276 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18940 | hp2 | a0003 | c0004 | t0003 | g0350 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18941 | hp2 | a0002 | c0002 | t0004 | g0141 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18942 | hp1 | a0003 | c0004 | t0003 | g0384 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18943 | hp1 | a0003 | c0007 | t0003 | g0361 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18945 | hp1 | a0008 | c0016 | t0002 | g0123 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18947 | hp2 | a0001 | c0003 | t0023 | g0248 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18948 | hp1 | a0001 | c0001 | t0008 | g0244 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0139 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18949 | hp2 | a0002 | c0002 | t0033 | g0039 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18951 | hp1 | a0002 | c0002 | t0004 | g0143 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18951 | hp2 | a0003 | c0004 | t0003 | g0012 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18959 | hp2 | a0003 | c0004 | t0003 | g0373 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18961 | hp1 | a0001 | c0003 | t0007 | g0278 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18961 | hp2 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18962 | hp2 | a0001 | c0003 | t0001 | g0259 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18965 | hp1 | a0003 | c0007 | t0002 | g0391 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18965 | hp2 | a0001 | c0001 | t0016 | g0265 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18967 | hp2 | a0005 | c0009 | t0001 | g0286 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0301 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18968 | hp2 | a0001 | c0003 | t0001 | g0285 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0313 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18969 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18971 | hp1 | a0002 | c0002 | t0004 | g0157 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18971 | hp2 | a0003 | c0004 | t0003 | g0356 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18972 | hp1 | a0001 | c0001 | t0008 | g0219 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18973 | hp2 | a0002 | c0002 | t0004 | g0101 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18974 | hp1 | a0001 | c0003 | t0030 | g0294 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18974 | hp2 | a0001 | c0003 | t0001 | g0315 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0319 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18975 | hp2 | a0003 | c0004 | t0003 | g0394 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18977 | hp1 | a0001 | c0003 | t0026 | g0268 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18977 | hp2 | a0001 | c0001 | t0018 | g0070 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18978 | hp1 | a0003 | c0004 | t0003 | g0372 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18978 | hp2 | a0002 | c0002 | t0004 | g0142 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18980 | hp1 | a0003 | c0004 | t0003 | g0349 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18980 | hp2 | a0001 | c0003 | t0007 | g0288 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18982 | hp1 | a0002 | c0002 | t0004 | g0100 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18984 | hp2 | a0001 | c0001 | t0008 | g0243 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0340 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18986 | hp1 | a0001 | c0001 | t0008 | g0218 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18986 | hp2 | a0003 | c0007 | t0002 | g0380 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18988 | hp1 | a0003 | c0007 | t0002 | g0363 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0234 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18993 | hp2 | a0003 | c0007 | t0002 | g0354 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18994 | hp2 | a0003 | c0004 | t0003 | g0365 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18995 | hp2 | a0001 | c0001 | t0017 | g0205 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18998 | hp1 | a0001 | c0001 | t0018 | g0165 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18998 | hp2 | a0001 | c0001 | t0008 | g0242 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0238 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19002 | hp1 | a0003 | c0004 | t0003 | g0388 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19003 | hp1 | a0001 | c0001 | t0022 | g0014 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19003 | hp2 | a0003 | c0004 | t0003 | g0393 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19004 | hp1 | a0001 | c0003 | t0007 | g0247 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19004 | hp2 | a0001 | c0001 | t0017 | g0077 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19005 | hp1 | a0001 | c0017 | t0001 | g0344 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0269 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0316 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19009 | hp1 | a0003 | c0004 | t0003 | g0012 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19009 | hp2 | a0001 | c0001 | t0032 | g0020 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19011 | hp1 | a0003 | c0004 | t0003 | g0355 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0332 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19030 | hp1 | a0001 | c0001 | t0035 | g0109 | AFR | LWK | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19030 | hp2 | a0002 | c0002 | t0005 | g0186 | AFR | LWK | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19054 | hp2 | a0001 | c0001 | t0008 | g0216 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19057 | hp1 | a0003 | c0007 | t0015 | g0360 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19057 | hp2 | a0001 | c0003 | t0001 | g0280 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19058 | hp1 | a0003 | c0004 | t0003 | g0370 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19060 | hp1 | a0001 | c0013 | t0002 | g0146 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19060 | hp2 | a0001 | c0003 | t0007 | g0306 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19062 | hp1 | a0003 | c0004 | t0001 | g0399 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19063 | hp2 | a0003 | c0004 | t0003 | g0376 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19065 | hp2 | a0003 | c0007 | t0002 | g0362 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19066 | hp1 | a0003 | c0007 | t0003 | g0389 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19066 | hp2 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19067 | hp2 | a0003 | c0004 | t0015 | g0382 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19068 | hp1 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19072 | hp2 | a0007 | c0019 | t0003 | g0352 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0314 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19077 | hp2 | a0002 | c0002 | t0004 | g0056 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19079 | hp2 | a0003 | c0004 | t0003 | g0383 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19080 | hp2 | a0003 | c0004 | t0003 | g0348 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19082 | hp2 | a0003 | c0004 | t0002 | g0358 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19083 | hp1 | a0003 | c0007 | t0002 | g0378 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19083 | hp2 | a0005 | c0009 | t0001 | g0190 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19086 | hp1 | a0003 | c0004 | t0003 | g0392 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19088 | hp1 | a0001 | c0001 | t0016 | g0150 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19090 | hp1 | a0003 | c0004 | t0003 | g0366 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19090 | hp2 | a0001 | c0003 | t0007 | g0311 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19091 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | YRI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA19240 | hp2 | a0002 | c0002 | t0006 | g0147 | AFR | YRI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20129 | hp1 | a0002 | c0002 | t0005 | g0091 | AFR | ASW | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ASW | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20752 | hp2 | a0004 | c0008 | t0001 | g0386 | EUR | TSI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | TSI | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20905 | hp1 | a0002 | c0002 | t0005 | g0256 | SAS | GIH | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | GIH | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01123 | hp1 | a0001 | c0001 | t0019 | g0067 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG01123 | hp2 | a0002 | c0005 | t0001 | g0185 | AMR | CLM | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0040 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02109 | hp2 | a0001 | c0006 | t0004 | g0320 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02486 | hp1 | a0002 | c0002 | t0011 | g0058 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02559 | hp1 | a0002 | c0015 | t0002 | g0260 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG03471 | hp2 | a0006 | c0010 | t0002 | g0346 | AFR | MSL | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | USA | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
HG06807 | hp2 | a0002 | c0002 | t0013 | g0087 | AFR | USA | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18955 | hp1 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA18955 | hp2 | a0003 | c0004 | t0003 | g0369 | EAS | JPT | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | USA | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0295 | AFR | LWK | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | LWK | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0005 | g0003 | REF | REF | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0270 | REF | REF | ENOSF1_chr18_665318_717630 | ENOSF1 | chr18 | 665318 | 717630 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:674325
|
G | A | 1 | a0009 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1312C>T | p.Leu438Phe | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1355/5362 | 1312/1332 | 438/443 | chr18 | 674325 | ||
chr18:681605
|
GTTTAAAT others(9044): Show |
G | 1 | a0005 | 2 | NA18967.hp2 NA19083.hp2 |
exon_loss_variant | HIGH | c.536-25_876+1640del | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/16 | chr18 | 681605 | ||||||
chr18:685988
|
G | A | 1 | a0007 | 1 | NA19072.hp2 | missense_variant | MODERATE | c.674C>T | p.Ala225Val | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/16 | 717/5362 | 674/1332 | 225/443 | chr18 | 685988 | ||
chr18:691266
|
A | G | 3 | a0002a0004a0009 | 90 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(87): Show |
missense_variant | MODERATE | c.434T>C | p.Met145Thr | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 6/16 | 477/5362 | 434/1332 | 145/443 | chr18 | 691266 | ||
chr18:706478
|
G | A | 1 | a0008 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.185C>T | p.Thr62Ile | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/16 | 228/5362 | 185/1332 | 62/443 | chr18 | 706478 | ||
chr18:706570
|
G | T | 1 | a0010 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.93C>A | p.Asp31Glu | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/16 | 136/5362 | 93/1332 | 31/443 | chr18 | 706570 | ||
chr18:712554
|
G | A | 1 | a0006 | 2 | HG03471.hp2 HG03540.hp1 |
missense_variant | MODERATE | c.34C>T | p.Arg12Trp | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/16 | 77/5362 | 34/1332 | 12/443 | chr18 | 712554 | ||
chr18:712568
|
G | A | 3 | a0003a0004a0007 | 62 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(59): Show |
missense_variant | MODERATE | c.20C>T | p.Ser7Phe | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/16 | 63/5362 | 20/1332 | 7/443 | chr18 | 712568 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:674320
|
A | G | 6 | a0001c0003a0001c0017a0002c0005others(3): Show | 64 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(61): Show |
synonymous_variant | LOW | c.1317T>C | p.Pro439Pro | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1360/5362 | 1317/1332 | 439/443 | chr18 | 674320 | ||
chr18:674401
|
G | A | 1 | a0002c0015 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1236C>T | p.Pro412Pro | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1279/5362 | 1236/1332 | 412/443 | chr18 | 674401 | ||
chr18:693888
|
C | T | 1 | a0001c0006 | 12 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
synonymous_variant | LOW | c.417G>A | p.Val139Val | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/16 | 460/5362 | 417/1332 | 139/443 | chr18 | 693888 | ||
chr18:706558
|
C | T | 5 | a0001c0013a0003c0004a0003c0018others(2): Show | 49 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(46): Show |
synonymous_variant | LOW | c.105G>A | p.Ser35Ser | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/16 | 148/5362 | 105/1332 | 35/443 | chr18 | 706558 | ||
chr18:712549
|
G | A | 1 | a0001c0017 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.39C>T | p.Asp13Asp | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/16 | 82/5362 | 39/1332 | 13/443 | chr18 | 712549 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:670414
|
C | T | 34 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(31): Show | 227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3891G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3891 | chr18 | 670414 | |||||
chr18:670472
|
C | T | 2 | a0002c0002t0011a0002c0002t0024 | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3833G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3833 | chr18 | 670472 | |||||
chr18:670541
|
A | G | 34 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(31): Show | 227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3764T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3764 | chr18 | 670541 | |||||
chr18:670551
|
G | A | 1 | a0001c0001t0017 | 2 | NA18995.hp2 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3754C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3754 | chr18 | 670551 | |||||
chr18:670618
|
C | T | 3 | a0002c0002t0011a0002c0002t0024a0002c0002t0031 | 8 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3687G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3687 | chr18 | 670618 | |||||
chr18:670888
|
T | C | 11 | a0001c0001t0006a0001c0001t0012a0001c0001t0020others(8): Show | 59 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3417A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3417 | chr18 | 670888 | |||||
chr18:670932
|
G | C | 1 | a0001c0001t0034 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3373C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3373 | chr18 | 670932 | |||||
chr18:670995
|
A | C | 44 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(41): Show | 266 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*3310T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3310 | chr18 | 670995 | |||||
chr18:671026
|
C | T | 33 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(30): Show | 226 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(223): Show |
3_prime_UTR_variant | MODIFIER | c.*3279G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3279 | chr18 | 671026 | |||||
chr18:671050
|
T | C | 2 | a0001c0001t0010a0003c0007t0010 | 6 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3255A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3255 | chr18 | 671050 | |||||
chr18:671057
|
C | T | 34 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(31): Show | 227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3248G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3248 | chr18 | 671057 | |||||
chr18:671105
|
T | C | 29 | a0001c0001t0002a0001c0001t0017a0001c0001t0018others(26): Show | 208 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(205): Show |
3_prime_UTR_variant | MODIFIER | c.*3200A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3200 | chr18 | 671105 | |||||
chr18:671167
|
G | A | 34 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(31): Show | 227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*3138C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3138 | chr18 | 671167 | |||||
chr18:671256
|
A | G | 1 | a0002c0002t0025 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3049T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3049 | chr18 | 671256 | |||||
chr18:671293
|
C | T | 1 | a0001c0001t0020 | 2 | HG02622.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3012G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 3012 | chr18 | 671293 | |||||
chr18:671520
|
C | T | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2785G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2785 | chr18 | 671520 | |||||
chr18:671648
|
A | T | 36 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(33): Show | 230 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2657T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2657 | chr18 | 671648 | |||||
chr18:671727
|
G | A | 31 | a0001c0001t0002a0001c0001t0016a0001c0001t0017others(28): Show | 212 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*2578C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2578 | chr18 | 671727 | |||||
chr18:671785
|
C | CT | 6 | a0001c0001t0014a0002c0002t0005a0002c0002t0013others(3): Show | 25 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2519dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2519 | chr18 | 671785 | |||||
chr18:671785
|
C | CTT | 1 | a0002c0002t0009 | 6 | HG02055.hp2 HG02258.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2518_*2519dupAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2519 | chr18 | 671785 | |||||
chr18:671785
|
CT | C | 34 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(31): Show | 228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*2519delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2519 | chr18 | 671785 | |||||
chr18:671834
|
C | T | 6 | a0001c0001t0014a0002c0002t0005a0002c0002t0009others(3): Show | 30 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2471G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2471 | chr18 | 671834 | |||||
chr18:671840
|
T | C | 2 | a0001c0001t0008a0001c0001t0022 | 9 | NA18948.hp1 NA18969.hp2 NA18972.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2465A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2465 | chr18 | 671840 | |||||
chr18:671977
|
A | G | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2328T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2328 | chr18 | 671977 | |||||
chr18:671988
|
C | T | 1 | a0001c0003t0026 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2317G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2317 | chr18 | 671988 | |||||
chr18:672035
|
C | T | 6 | a0001c0001t0014a0002c0002t0005a0002c0002t0009others(3): Show | 30 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2270G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2270 | chr18 | 672035 | |||||
chr18:672043
|
A | G | 41 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(38): Show | 259 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*2262T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2262 | chr18 | 672043 | |||||
chr18:672168
|
C | A | 1 | a0001c0001t0018 | 2 | NA18977.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2137G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2137 | chr18 | 672168 | |||||
chr18:672204
|
T | G | 1 | a0006c0010t0029 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2101A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2101 | chr18 | 672204 | |||||
chr18:672279
|
T | TAAAAGTT others(40): Show |
1 | a0001c0003t0030 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2025_*2026insTTTT others(43): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2025 | chr18 | 672279 | |||||
chr18:672288
|
C | T | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*2017G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 2017 | chr18 | 672288 | |||||
chr18:672363
|
G | A | 38 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(35): Show | 237 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*1942C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1942 | chr18 | 672363 | |||||
chr18:672393
|
G | GTCTTCAC others(19): Show |
1 | a0003c0004t0036 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1886_*1911dupAGAC others(22): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1911 | chr18 | 672393 | |||||
chr18:672590
|
G | A | 1 | a0001c0001t0019 | 2 | HG00323.hp1 HG01123.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1715C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1715 | chr18 | 672590 | |||||
chr18:672595
|
G | T | 1 | a0001c0001t0035 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1710C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1710 | chr18 | 672595 | |||||
chr18:672599
|
T | C | 1 | a0001c0001t0038 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1706A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1706 | chr18 | 672599 | |||||
chr18:672792
|
C | T | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1513G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1513 | chr18 | 672792 | |||||
chr18:672836
|
A | G | 6 | a0001c0001t0014a0002c0002t0005a0002c0002t0009others(3): Show | 30 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1469T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1469 | chr18 | 672836 | |||||
chr18:673016
|
C | T | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1289G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1289 | chr18 | 673016 | |||||
chr18:673059
|
G | C | 1 | a0001c0001t0039 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1246C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1246 | chr18 | 673059 | |||||
chr18:673086
|
A | G | 19 | a0001c0001t0002a0001c0001t0016a0001c0001t0017others(16): Show | 135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*1219T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1219 | chr18 | 673086 | |||||
chr18:673211
|
G | T | 1 | a0001c0001t0012 | 6 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1094 | chr18 | 673211 | |||||
chr18:673256
|
TG | T | 1 | a0002c0002t0013 | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1048delC | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 1048 | chr18 | 673256 | |||||
chr18:673395
|
G | A | 3 | a0001c0001t0006a0001c0001t0012a0002c0002t0006 | 16 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*910C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 910 | chr18 | 673395 | |||||
chr18:673443
|
TTTAAAG | T | 34 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(31): Show | 228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*856_*861delCTTTAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 856 | chr18 | 673443 | |||||
chr18:673613
|
A | G | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*692T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 692 | chr18 | 673613 | |||||
chr18:673710
|
G | GT | 7 | a0001c0001t0007a0001c0001t0014a0001c0003t0007others(4): Show | 12 | HG00544.hp2 HG01192.hp2 HG02738.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*594dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 594 | chr18 | 673710 | |||||
chr18:673710
|
GTTT | G | 30 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(27): Show | 224 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*592_*594delAAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 592 | chr18 | 673710 | |||||
chr18:673732
|
CTT | C | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*571_*572delAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 571 | chr18 | 673732 | |||||
chr18:673789
|
A | G | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*516T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 516 | chr18 | 673789 | |||||
chr18:673995
|
T | C | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*310A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 310 | chr18 | 673995 | |||||
chr18:674012
|
T | G | 35 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(32): Show | 229 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*293A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 16/16 | 293 | chr18 | 674012 | |||||
chr18:712590
|
C | T | 1 | a0001c0001t0022 | 1 | NA19003.hp1 | 5_prime_UTR_variant | MODIFIER | c.-3G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/16 | 3 | chr18 | 712590 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:674440
|
A | C | 202 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(199): Show | 212 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1231-34T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674440 | ||||||
chr18:674535
|
T | C | 240 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(237): Show | 251 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.1231-129A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674535 | ||||||
chr18:674579
|
C | T | 19 | a0001c0003t0001g0023a0001c0003t0001g0253a0001c0003t0001g0284others(16): Show | 20 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231-173G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674579 | ||||||
chr18:674645
|
T | C | 218 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(215): Show | 228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.1231-239A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674645 | ||||||
chr18:674693
|
T | C | 1 | a0002c0002t0004g0056 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1231-287A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674693 | ||||||
chr18:674744
|
A | C | 1 | a0001c0003t0001g0341 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1231-338T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674744 | ||||||
chr18:674852
|
C | T | 16 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(13): Show | 16 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1231-446G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 674852 | ||||||
chr18:675000
|
C | T | 217 | a0001c0001t0001g0327a0001c0001t0002g0001a0001c0001t0002g0004others(214): Show | 227 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.1230+321G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675000 | ||||||
chr18:675007
|
T | C | 1 | a0002c0002t0004g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1230+314A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675007 | ||||||
chr18:675272
|
C | T | 20 | a0001c0001t0002g0033a0001c0001t0006g0042a0001c0001t0006g0107others(17): Show | 20 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.1230+49G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675272 | ||||||
chr18:675300
|
G | T | 1 | a0002c0002t0004g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1230+21C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675300 | ||||||
chr18:675307
|
A | G | 54 | a0001c0001t0001g0343a0001c0001t0002g0074a0001c0001t0002g0198others(51): Show | 55 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1230+14T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 15/15 | chr18 | 675307 | ||||||
chr18:675643
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1149-241A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675643 | ||||||
chr18:675774
|
T | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(163): Show | 174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-372A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675774 | ||||||
chr18:675787
|
C | T | 295 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0108others(292): Show | 307 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.1149-385G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675787 | ||||||
chr18:675789
|
T | C | 39 | a0001c0001t0020g0191a0001c0001t0020g0236a0003c0004t0001g0399others(36): Show | 41 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1149-387A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675789 | ||||||
chr18:675816
|
G | A | 1 | a0001c0003t0001g0291 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1149-414C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675816 | ||||||
chr18:675821
|
T | TAA | 166 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(163): Show | 174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-420_1149-419i others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675821 | ||||||
chr18:675822
|
T | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(163): Show | 174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-420A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675822 | ||||||
chr18:675823
|
T | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(163): Show | 174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-421A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675823 | ||||||
chr18:675824
|
T | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(163): Show | 174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-422A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675824 | ||||||
chr18:675825
|
G | A | 166 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(163): Show | 174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1149-423C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675825 | ||||||
chr18:675903
|
C | T | 164 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(161): Show | 172 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1149-501G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 675903 | ||||||
chr18:676008
|
G | C | 272 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(269): Show | 284 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.1149-606C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676008 | ||||||
chr18:676030
|
A | G | 3 | a0001c0003t0001g0341a0003c0011t0001g0401a0003c0011t0001g0402 | 3 | HG02683.hp1 HG03654.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1149-628T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676030 | ||||||
chr18:676059
|
A | T | 8 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149-657T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676059 | ||||||
chr18:676139
|
T | G | 1 | a0001c0001t0002g0303 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1149-737A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676139 | ||||||
chr18:676228
|
T | A | 64 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(61): Show | 66 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1149-826A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676228 | ||||||
chr18:676293
|
T | A | 2 | a0001c0001t0002g0115a0001c0001t0002g0166 | 2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1149-891A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676293 | ||||||
chr18:676329
|
G | C | 2 | a0001c0001t0020g0191a0001c0001t0020g0236 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1149-927C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676329 | ||||||
chr18:676331
|
G | C | 63 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(60): Show | 65 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1149-929C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676331 | ||||||
chr18:676403
|
T | TTC | 165 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(162): Show | 173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1148+940_1148+941d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676403 | ||||||
chr18:676473
|
C | T | 68 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(65): Show | 73 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.1148+872G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676473 | ||||||
chr18:676490
|
G | C | 60 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(57): Show | 62 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1148+855C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676490 | ||||||
chr18:676518
|
T | C | 167 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(164): Show | 175 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1148+827A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676518 | ||||||
chr18:676711
|
C | A | 1 | a0001c0001t0006g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1148+634G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676711 | ||||||
chr18:676789
|
A | T | 72 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(69): Show | 76 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(73): Show |
intron_variant | MODIFIER | c.1148+556T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676789 | ||||||
chr18:676924
|
G | T | 1 | a0002c0002t0005g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1148+421C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676924 | ||||||
chr18:676940
|
T | C | 1 | a0003c0004t0003g0366 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1148+405A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 676940 | ||||||
chr18:677214
|
G | A | 165 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(162): Show | 173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1148+131C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 677214 | ||||||
chr18:677240
|
G | A | 166 | a0001c0001t0001g0215a0001c0001t0002g0001a0001c0001t0002g0004others(163): Show | 174 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1148+105C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 677240 | ||||||
chr18:677302
|
G | A | 165 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(162): Show | 173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1148+43C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 14/15 | chr18 | 677302 | ||||||
chr18:677452
|
G | A | 1 | a0002c0002t0004g0181 | 1 | HG01496.hp2 | splice_region_variant&intron_variant | LOW | c.1049-8C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677452 | ||||||
chr18:677621
|
T | G | 23 | a0002c0002t0004g0024a0002c0002t0004g0025a0002c0002t0004g0056others(20): Show | 24 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1048+122A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677621 | ||||||
chr18:677677
|
A | G | 2 | a0002c0002t0009g0089a0002c0002t0009g0090 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1048+66T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677677 | ||||||
chr18:677736
|
C | T | 1 | a0001c0001t0039g0312 | 1 | HG01109.hp2 | splice_region_variant&intron_variant | LOW | c.1048+7G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677736 | ||||||
chr18:677737
|
G | A | 1 | a0001c0003t0023g0248 | 1 | NA18947.hp2 | splice_region_variant&intron_variant | LOW | c.1048+6C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 13/15 | chr18 | 677737 | ||||||
chr18:677931
|
C | G | 132 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(129): Show | 136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.919-59G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 677931 | ||||||
chr18:677944
|
C | T | 1 | a0009c0014t0027g0156 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919-72G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 677944 | ||||||
chr18:677970
|
T | G | 13 | a0001c0001t0002g0028a0001c0001t0002g0044a0001c0001t0002g0045others(10): Show | 13 | HG01106.hp2 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.919-98A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 677970 | ||||||
chr18:677992
|
C | A | 1 | a0002c0002t0005g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.919-120G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 677992 | ||||||
chr18:678124
|
G | A | 1 | a0009c0014t0027g0156 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.919-252C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678124 | ||||||
chr18:678135
|
G | A | 1 | a0002c0002t0005g0212 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.919-263C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678135 | ||||||
chr18:678158
|
A | G | 4 | a0001c0001t0001g0222a0001c0001t0001g0258a0001c0001t0001g0292others(1): Show | 4 | HG00639.hp2 HG01261.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-286T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678158 | ||||||
chr18:678235
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.919-363G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678235 | ||||||
chr18:678481
|
C | T | 165 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(162): Show | 173 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.918+215G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678481 | ||||||
chr18:678499
|
T | C | 6 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0048others(3): Show | 6 | NA18941.hp1 NA18984.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.918+197A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678499 | ||||||
chr18:678666
|
C | T | 1 | a0001c0003t0001g0340 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.918+30G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 12/15 | chr18 | 678666 | ||||||
chr18:678847
|
T | C | 40 | a0001c0001t0014g0300a0001c0003t0001g0284a0002c0002t0005g0003others(37): Show | 42 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.877-110A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 678847 | ||||||
chr18:678929
|
G | A | 1 | a0003c0004t0003g0347 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.877-192C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 678929 | ||||||
chr18:678947
|
A | G | 276 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(273): Show | 288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.877-210T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 678947 | ||||||
chr18:679001
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.877-264C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679001 | ||||||
chr18:679031
|
G | A | 8 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.877-294C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679031 | ||||||
chr18:679042
|
C | T | 5 | a0001c0003t0001g0241a0001c0003t0001g0253a0001c0003t0001g0262others(2): Show | 5 | HG00673.hp2 HG02040.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-305G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679042 | ||||||
chr18:679067
|
A | G | 1 | a0001c0001t0038g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.877-330T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679067 | ||||||
chr18:679150
|
C | T | 5 | a0002c0002t0013g0018a0002c0002t0013g0087a0002c0002t0013g0130others(2): Show | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-413G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679150 | ||||||
chr18:679199
|
CTCTCA | C | 10 | a0001c0001t0001g0221a0001c0001t0001g0255a0001c0001t0001g0282others(7): Show | 10 | HG00280.hp2 HG01074.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.877-467_877-463del others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679199 | ||||||
chr18:679202
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.877-465A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679202 | ||||||
chr18:679208
|
C | CT | 64 | a0001c0001t0001g0324a0001c0001t0008g0216a0001c0001t0010g0257others(61): Show | 66 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.877-472dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679208 | ||||||
chr18:679208
|
CT | C | 11 | a0001c0001t0001g0263a0001c0001t0002g0022a0001c0001t0002g0034others(8): Show | 13 | HG00408.hp1 HG01070.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.877-472delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679208 | ||||||
chr18:679208
|
CTT | C | 154 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(151): Show | 160 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.877-473_877-472del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679208 | ||||||
chr18:679208
|
CTTT | C | 9 | a0001c0001t0002g0118a0001c0001t0002g0203a0001c0003t0001g0269others(6): Show | 9 | NA18967.hp2 NA18977.hp1 NA18981.hp1 others(6): Show |
intron_variant | MODIFIER | c.877-474_877-472del others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679208 | ||||||
chr18:679300
|
C | G | 6 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0012g0059others(3): Show | 6 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.877-563G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679300 | ||||||
chr18:679334
|
T | C | 276 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(273): Show | 288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.877-597A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679334 | ||||||
chr18:679335
|
G | A | 1 | a0008c0016t0002g0123 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.877-598C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679335 | ||||||
chr18:679353
|
G | A | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.877-616C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679353 | ||||||
chr18:679375
|
A | AT | 40 | a0001c0001t0014g0300a0001c0003t0001g0284a0002c0002t0005g0003others(37): Show | 42 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.877-639dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679375 | ||||||
chr18:679398
|
A | G | 40 | a0001c0001t0014g0300a0001c0003t0001g0284a0002c0002t0005g0003others(37): Show | 42 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.877-661T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679398 | ||||||
chr18:679449
|
T | TCC | 173 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(170): Show | 181 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.877-714_877-713dup others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679449 | ||||||
chr18:679561
|
GA | G | 203 | a0001c0001t0002g0017a0001c0001t0002g0021a0001c0001t0002g0022others(200): Show | 211 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.877-825delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679561 | ||||||
chr18:679561
|
GAA | G | 71 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 75 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.877-826_877-825del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679561 | ||||||
chr18:679626
|
G | T | 1 | a0001c0003t0001g0241 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.877-889C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679626 | ||||||
chr18:679637
|
T | C | 61 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0012g0059others(58): Show | 63 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.877-900A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679637 | ||||||
chr18:679653
|
G | C | 40 | a0001c0001t0020g0191a0001c0001t0020g0236a0003c0004t0001g0399others(37): Show | 42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.877-916C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679653 | ||||||
chr18:679660
|
C | G | 70 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(67): Show | 72 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.877-923G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679660 | ||||||
chr18:679769
|
C | G | 1 | a0001c0001t0034g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.877-1032G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679769 | ||||||
chr18:679878
|
C | T | 40 | a0001c0001t0020g0191a0001c0001t0020g0236a0003c0004t0001g0399others(37): Show | 42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.877-1141G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679878 | ||||||
chr18:679990
|
T | TA | 9 | a0001c0001t0034g0105a0002c0002t0011g0058a0002c0002t0011g0103others(6): Show | 9 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.877-1254dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 679990 | ||||||
chr18:680312
|
T | C | 40 | a0001c0001t0020g0191a0001c0001t0020g0236a0003c0004t0001g0399others(37): Show | 42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.877-1575A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680312 | ||||||
chr18:680373
|
G | A | 1 | a0001c0001t0012g0059 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.877-1636C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680373 | ||||||
chr18:680380
|
C | T | 182 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(179): Show | 190 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.877-1643G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680380 | ||||||
chr18:680520
|
A | C | 141 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(138): Show | 148 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.877-1783T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680520 | ||||||
chr18:680590
|
A | G | 2 | a0001c0003t0001g0262a0001c0003t0001g0301 | 2 | NA18961.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.877-1853T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680590 | ||||||
chr18:680676
|
G | GT | 7 | a0001c0001t0008g0219a0001c0001t0028g0304a0001c0003t0001g0285others(4): Show | 7 | HG02698.hp1 HG04115.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.877-1940dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680676 | ||||||
chr18:680676
|
GT | G | 68 | a0001c0001t0001g0274a0001c0001t0006g0154a0001c0001t0008g0218others(65): Show | 70 | HG00280.hp1 HG00621.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.877-1940delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680676 | ||||||
chr18:680676
|
GTT | G | 204 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(201): Show | 214 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.877-1941_877-1940d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680676 | ||||||
chr18:680685
|
T | G | 5 | a0002c0002t0013g0018a0002c0002t0013g0087a0002c0002t0013g0130others(2): Show | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.877-1948A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680685 | ||||||
chr18:680687
|
T | G | 23 | a0002c0002t0004g0024a0002c0002t0004g0025a0002c0002t0004g0056others(20): Show | 24 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.877-1950A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680687 | ||||||
chr18:680742
|
G | A | 1 | a0001c0003t0030g0294 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.877-2005C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680742 | ||||||
chr18:680838
|
G | A | 181 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(178): Show | 189 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.877-2101C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680838 | ||||||
chr18:680985
|
T | C | 71 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 75 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.877-2248A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 680985 | ||||||
chr18:681047
|
A | T | 40 | a0001c0001t0020g0191a0001c0001t0020g0236a0003c0004t0001g0399others(37): Show | 42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.876+2199T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681047 | ||||||
chr18:681051
|
G | A | 1 | a0002c0002t0005g0134 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.876+2195C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681051 | ||||||
chr18:681077
|
G | C | 9 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(6): Show | 9 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+2169C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681077 | ||||||
chr18:681145
|
AGCCACTA others(6): Show |
A | 1 | a0010c0012t0002g0169 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.876+2088_876+2100d others(15): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681145 | ||||||
chr18:681192
|
G | A | 400 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(397): Show | 416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.876+2054C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681192 | ||||||
chr18:681267
|
T | G | 9 | a0001c0006t0004g0002a0001c0006t0004g0006a0001c0006t0004g0148others(6): Show | 12 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.876+1979A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681267 | ||||||
chr18:681469
|
C | T | 1 | a0001c0001t0039g0312 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.876+1777G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681469 | ||||||
chr18:681624
|
T | C | 1 | a0003c0004t0002g0358 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.876+1622A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681624 | ||||||
chr18:681724
|
C | T | 53 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0012g0059others(50): Show | 55 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.876+1522G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681724 | ||||||
chr18:681779
|
A | G | 1 | a0009c0014t0027g0156 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.876+1467T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681779 | ||||||
chr18:681823
|
G | A | 38 | a0003c0004t0001g0399a0003c0004t0003g0012a0003c0004t0003g0013others(35): Show | 40 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.876+1423C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681823 | ||||||
chr18:681927
|
T | C | 1 | a0002c0002t0004g0144 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.876+1319A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681927 | ||||||
chr18:681962
|
G | A | 164 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(161): Show | 172 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.876+1284C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 681962 | ||||||
chr18:682260
|
C | T | 1 | a0001c0001t0034g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.876+986G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682260 | ||||||
chr18:682399
|
C | T | 12 | a0001c0001t0014g0300a0002c0002t0002g0098a0002c0002t0005g0003others(9): Show | 13 | HG01106.hp1 HG01192.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.876+847G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682399 | ||||||
chr18:682411
|
A | G | 1 | a0001c0003t0001g0269 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.876+835T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682411 | ||||||
chr18:682466
|
A | G | 1 | a0003c0007t0002g0363 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.876+780T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682466 | ||||||
chr18:682470
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.876+776A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682470 | ||||||
chr18:682715
|
C | CA | 38 | a0001c0001t0001g0108a0001c0001t0001g0194a0001c0001t0001g0277others(35): Show | 41 | HG00597.hp2 HG01123.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.876+530dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682715 | ||||||
chr18:682715
|
C | CAA | 10 | a0001c0006t0004g0148a0002c0002t0011g0058a0002c0002t0011g0103others(7): Show | 10 | HG01884.hp1 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.876+529_876+530dup others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682715 | ||||||
chr18:682715
|
C | CAAA | 34 | a0001c0001t0020g0191a0003c0004t0001g0399a0003c0004t0003g0012others(31): Show | 36 | HG00423.hp1 HG00621.hp2 HG02004.hp1 others(33): Show |
intron_variant | MODIFIER | c.876+528_876+530dup others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682715 | ||||||
chr18:682723
|
A | AT | 9 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(6): Show | 9 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+522_876+523ins others(1): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682723 | ||||||
chr18:682881
|
TCAAAA | T | 103 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(100): Show | 107 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.876+360_876+364del others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682881 | ||||||
chr18:682922
|
C | CA | 72 | a0001c0001t0001g0261a0001c0001t0020g0191a0001c0003t0001g0284others(69): Show | 75 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.876+323dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682922 | ||||||
chr18:682922
|
C | CAA | 18 | a0001c0001t0014g0300a0001c0001t0020g0236a0002c0002t0002g0098others(15): Show | 19 | HG01106.hp1 HG01192.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.876+322_876+323dup others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682922 | ||||||
chr18:682922
|
CA | C | 9 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(6): Show | 9 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+323delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682922 | ||||||
chr18:682925
|
A | AC | 7 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0012g0059others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.876+320_876+321ins others(1): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682925 | ||||||
chr18:682926
|
A | C | 9 | a0001c0001t0001g0275a0002c0002t0011g0058a0002c0002t0011g0103others(6): Show | 9 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.876+320T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682926 | ||||||
chr18:682941
|
C | T | 5 | a0002c0002t0013g0018a0002c0002t0013g0087a0002c0002t0013g0130others(2): Show | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.876+305G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 682941 | ||||||
chr18:683001
|
C | A | 1 | a0009c0014t0027g0156 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.876+245G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 683001 | ||||||
chr18:683094
|
C | G | 54 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0012g0059others(51): Show | 56 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.876+152G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 683094 | ||||||
chr18:683116
|
C | G | 41 | a0001c0001t0014g0300a0001c0003t0001g0284a0002c0002t0002g0098others(38): Show | 43 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.876+130G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 683116 | ||||||
chr18:683126
|
A | G | 3 | a0002c0002t0004g0100a0002c0002t0004g0141a0002c0002t0033g0039 | 3 | NA18941.hp2 NA18949.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.876+120T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 11/15 | chr18 | 683126 | ||||||
chr18:683440
|
C | T | 40 | a0001c0001t0020g0191a0001c0001t0020g0236a0003c0004t0001g0399others(37): Show | 42 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.742-60G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683440 | ||||||
chr18:683441
|
G | A | 140 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(137): Show | 147 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.742-61C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683441 | ||||||
chr18:683452
|
A | G | 9 | a0001c0006t0004g0002a0001c0006t0004g0006a0001c0006t0004g0148others(6): Show | 12 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-72T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683452 | ||||||
chr18:683525
|
G | A | 1 | a0001c0001t0012g0059 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742-145C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683525 | ||||||
chr18:683573
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.742-193C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683573 | ||||||
chr18:683607
|
C | T | 276 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0015others(273): Show | 288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.742-227G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683607 | ||||||
chr18:683664
|
C | T | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.742-284G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683664 | ||||||
chr18:683732
|
G | A | 1 | a0001c0001t0034g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.742-352C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683732 | ||||||
chr18:683766
|
A | ACATTGTT others(1): Show |
24 | a0001c0001t0002g0017a0001c0001t0002g0022a0001c0001t0002g0029others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.742-387_742-386ins others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683766 | ||||||
chr18:683767
|
A | G | 24 | a0001c0001t0002g0017a0001c0001t0002g0022a0001c0001t0002g0029others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.742-387T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683767 | ||||||
chr18:683861
|
T | C | 40 | a0001c0001t0014g0300a0001c0003t0001g0284a0002c0002t0002g0098others(37): Show | 42 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.742-481A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683861 | ||||||
chr18:683901
|
T | C | 9 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(6): Show | 9 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.742-521A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683901 | ||||||
chr18:683919
|
A | G | 1 | a0002c0002t0031g0337 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.742-539T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683919 | ||||||
chr18:683984
|
ATTTCT | A | 11 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(8): Show | 11 | HG02257.hp1 HG02615.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.742-609_742-605del others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683984 | ||||||
chr18:683999
|
CT | C | 73 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0012g0059others(70): Show | 75 | HG00280.hp1 HG00423.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.742-620delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683999 | ||||||
chr18:683999
|
CTT | C | 9 | a0001c0001t0020g0191a0003c0004t0003g0013a0003c0004t0003g0348others(6): Show | 10 | HG00438.hp2 HG00621.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.742-621_742-620del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 683999 | ||||||
chr18:684025
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.742-645C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684025 | ||||||
chr18:684048
|
C | T | 119 | a0001c0001t0001g0055a0001c0001t0001g0180a0001c0001t0002g0001others(116): Show | 123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.742-668G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684048 | ||||||
chr18:684063
|
G | A | 1 | a0003c0004t0036g0364 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.742-683C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684063 | ||||||
chr18:684112
|
G | A | 1 | a0002c0005t0001g0019 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.742-732C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684112 | ||||||
chr18:684139
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.742-759C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684139 | ||||||
chr18:684177
|
A | G | 6 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.742-797T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684177 | ||||||
chr18:684185
|
C | T | 1 | a0002c0002t0004g0183 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.742-805G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684185 | ||||||
chr18:684197
|
A | G | 11 | a0002c0002t0002g0098a0002c0002t0004g0183a0002c0002t0005g0003others(8): Show | 12 | HG01106.hp1 HG01433.hp1 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.742-817T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684197 | ||||||
chr18:684217
|
A | C | 1 | a0001c0001t0028g0304 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.742-837T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684217 | ||||||
chr18:684287
|
A | G | 94 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0012g0059others(91): Show | 96 | HG00280.hp1 HG00423.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.742-907T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684287 | ||||||
chr18:684335
|
C | T | 43 | a0001c0001t0020g0191a0001c0001t0020g0236a0003c0004t0001g0399others(40): Show | 45 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.742-955G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684335 | ||||||
chr18:684371
|
T | C | 1 | a0002c0002t0006g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.742-991A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684371 | ||||||
chr18:684373
|
C | T | 1 | a0001c0001t0038g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.742-993G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684373 | ||||||
chr18:684523
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.742-1143A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684523 | ||||||
chr18:684570
|
C | T | 13 | a0001c0001t0012g0040a0001c0001t0012g0041a0001c0001t0012g0059others(10): Show | 13 | HG01109.hp1 HG01192.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.742-1190G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684570 | ||||||
chr18:684766
|
T | C | 288 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(285): Show | 300 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.741+1155A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684766 | ||||||
chr18:684846
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.741+1075T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684846 | ||||||
chr18:684864
|
AT | A | 81 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0275others(78): Show | 81 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.741+1056delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684864 | ||||||
chr18:684993
|
G | A | 1 | a0001c0001t0006g0226 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.741+928C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 684993 | ||||||
chr18:685026
|
A | AT | 379 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(376): Show | 395 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.741+894dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685026 | ||||||
chr18:685075
|
G | A | 7 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.741+846C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685075 | ||||||
chr18:685158
|
G | C | 64 | a0001c0001t0006g0225a0001c0001t0012g0040a0001c0001t0012g0041others(61): Show | 66 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.741+763C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685158 | ||||||
chr18:685165
|
CT | C | 13 | a0002c0002t0001g0099a0002c0005t0001g0005a0002c0005t0001g0019others(10): Show | 14 | HG00642.hp2 HG01123.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.741+755delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685165 | ||||||
chr18:685198
|
G | T | 2 | a0001c0001t0001g0323a0001c0001t0001g0334 | 2 | HG00597.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.741+723C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685198 | ||||||
chr18:685239
|
C | T | 5 | a0001c0001t0001g0334a0001c0001t0012g0040a0001c0001t0012g0041others(2): Show | 5 | HG00597.hp2 HG01109.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.741+682G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685239 | ||||||
chr18:685340
|
T | C | 1 | a0001c0001t0001g0217 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.741+581A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685340 | ||||||
chr18:685392
|
T | C | 2 | a0001c0001t0020g0191a0001c0001t0020g0236 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.741+529A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685392 | ||||||
chr18:685447
|
A | G | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.741+474T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685447 | ||||||
chr18:685511
|
T | C | 51 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(48): Show | 53 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.741+410A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685511 | ||||||
chr18:685574
|
T | G | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.741+347A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685574 | ||||||
chr18:685627
|
CAT | C | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.741+292_741+293del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685627 | ||||||
chr18:685671
|
G | A | 1 | a0001c0001t0006g0153 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.741+250C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685671 | ||||||
chr18:685692
|
A | C | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.741+229T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685692 | ||||||
chr18:685706
|
C | G | 2 | a0002c0002t0005g0289a0002c0002t0005g0290 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.741+215G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685706 | ||||||
chr18:685783
|
G | A | 4 | a0001c0001t0002g0062a0001c0001t0002g0195a0001c0001t0002g0196others(1): Show | 4 | HG03017.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+138C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685783 | ||||||
chr18:685797
|
C | T | 278 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(275): Show | 290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.741+124G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685797 | ||||||
chr18:685799
|
C | T | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.741+122G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685799 | ||||||
chr18:685818
|
A | G | 42 | a0001c0013t0002g0146a0003c0004t0001g0399a0003c0004t0002g0395others(39): Show | 44 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.741+103T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685818 | ||||||
chr18:685861
|
G | A | 2 | a0002c0002t0009g0093a0002c0002t0009g0133 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.741+60C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 10/15 | chr18 | 685861 | ||||||
chr18:686055
|
G | A | 1 | a0001c0003t0001g0239 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.654-47C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686055 | ||||||
chr18:686151
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.654-143T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686151 | ||||||
chr18:686289
|
C | T | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.654-281G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686289 | ||||||
chr18:686370
|
A | G | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-362T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686370 | ||||||
chr18:686386
|
G | T | 2 | a0001c0001t0020g0191a0001c0001t0020g0236 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.654-378C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686386 | ||||||
chr18:686662
|
C | T | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-654G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686662 | ||||||
chr18:686669
|
T | C | 1 | a0006c0010t0029g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.654-661A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686669 | ||||||
chr18:686738
|
C | T | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.654-730G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686738 | ||||||
chr18:686782
|
C | T | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-774G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686782 | ||||||
chr18:686788
|
G | C | 1 | a0002c0005t0001g0064 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.654-780C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686788 | ||||||
chr18:686807
|
C | T | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-799G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686807 | ||||||
chr18:686858
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.654-850C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 686858 | ||||||
chr18:687009
|
CAGAT | C | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-1005_654-1002d others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687009 | ||||||
chr18:687017
|
C | T | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-1009G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687017 | ||||||
chr18:687031
|
C | T | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.654-1023G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687031 | ||||||
chr18:687045
|
G | A | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-1037C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687045 | ||||||
chr18:687055
|
A | ACAGC | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-1051_654-1048d others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687055 | ||||||
chr18:687056
|
C | T | 3 | a0001c0001t0006g0042a0001c0001t0006g0154a0001c0001t0006g0155 | 3 | HG02630.hp1 HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.654-1048G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687056 | ||||||
chr18:687119
|
G | T | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-1111C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687119 | ||||||
chr18:687192
|
C | T | 1 | a0001c0001t0012g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.654-1184G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687192 | ||||||
chr18:687208
|
C | G | 53 | a0001c0001t0020g0191a0001c0001t0020g0236a0002c0002t0001g0092others(50): Show | 55 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.654-1200G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687208 | ||||||
chr18:687223
|
G | A | 5 | a0002c0002t0013g0018a0002c0002t0013g0087a0002c0002t0013g0130others(2): Show | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.654-1215C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687223 | ||||||
chr18:687261
|
T | A | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-1253A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687261 | ||||||
chr18:687267
|
C | T | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.654-1259G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687267 | ||||||
chr18:687270
|
G | A | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.654-1262C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687270 | ||||||
chr18:687410
|
C | T | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.653+1164G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687410 | ||||||
chr18:687534
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.653+1040C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687534 | ||||||
chr18:687850
|
G | A | 2 | a0001c0001t0020g0191a0001c0001t0020g0236 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.653+724C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687850 | ||||||
chr18:687879
|
C | T | 1 | a0010c0012t0002g0169 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.653+695G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687879 | ||||||
chr18:687904
|
C | A | 57 | a0001c0006t0004g0149a0002c0002t0001g0092a0002c0002t0001g0099others(54): Show | 59 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.653+670G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687904 | ||||||
chr18:687914
|
C | G | 2 | a0002c0002t0009g0026a0009c0014t0027g0156 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.653+660G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 687914 | ||||||
chr18:688012
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.653+562G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688012 | ||||||
chr18:688040
|
G | A | 1 | a0002c0005t0001g0210 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.653+534C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688040 | ||||||
chr18:688103
|
C | G | 332 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0053others(329): Show | 346 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.653+471G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688103 | ||||||
chr18:688123
|
C | T | 8 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.653+451G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688123 | ||||||
chr18:688139
|
T | C | 42 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(39): Show | 44 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.653+435A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688139 | ||||||
chr18:688167
|
C | CA | 106 | a0001c0001t0002g0017a0001c0001t0002g0021a0001c0001t0002g0022others(103): Show | 110 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.653+406dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688167 | ||||||
chr18:688167
|
C | CAA | 123 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(120): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.653+405_653+406dup others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688167 | ||||||
chr18:688167
|
C | CAAA | 6 | a0002c0002t0005g0178a0002c0002t0005g0179a0002c0005t0001g0063others(3): Show | 6 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.653+404_653+406dup others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688167 | ||||||
chr18:688190
|
G | T | 2 | a0001c0001t0002g0171a0001c0001t0002g0229 | 2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.653+384C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688190 | ||||||
chr18:688191
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.653+383T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688191 | ||||||
chr18:688428
|
G | A | 86 | a0001c0001t0020g0191a0001c0001t0020g0236a0002c0002t0001g0092others(83): Show | 89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.653+146C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688428 | ||||||
chr18:688441
|
T | C | 9 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.653+133A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688441 | ||||||
chr18:688442
|
A | C | 1 | a0002c0002t0004g0183 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.653+132T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688442 | ||||||
chr18:688463
|
G | T | 277 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(274): Show | 289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.653+111C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 9/15 | chr18 | 688463 | ||||||
chr18:688711
|
T | C | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-103A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 688711 | ||||||
chr18:689018
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.619-410C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689018 | ||||||
chr18:689021
|
T | G | 1 | a0002c0002t0009g0131 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.619-413A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689021 | ||||||
chr18:689070
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.619-462A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689070 | ||||||
chr18:689142
|
C | T | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.619-534G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689142 | ||||||
chr18:689232
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.619-624G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689232 | ||||||
chr18:689242
|
G | C | 129 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(126): Show | 136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.619-634C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689242 | ||||||
chr18:689333
|
G | T | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.619-725C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689333 | ||||||
chr18:689437
|
C | T | 8 | a0002c0002t0002g0098a0002c0002t0005g0003a0002c0002t0005g0097others(5): Show | 9 | HG01256.hp1 HG01433.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-829G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689437 | ||||||
chr18:689660
|
G | T | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.618+889C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689660 | ||||||
chr18:689665
|
A | G | 26 | a0002c0002t0002g0319a0002c0002t0004g0024a0002c0002t0004g0025others(23): Show | 27 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.618+884T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689665 | ||||||
chr18:689680
|
TCTGCCCC others(5): Show |
T | 1 | a0001c0001t0020g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.618+857_618+868del others(12): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689680 | ||||||
chr18:689693
|
C | T | 1 | a0001c0001t0039g0312 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.618+856G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689693 | ||||||
chr18:689748
|
CTGAG | C | 5 | a0002c0002t0013g0018a0002c0002t0013g0087a0002c0002t0013g0130others(2): Show | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+797_618+800del others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689748 | ||||||
chr18:689779
|
C | T | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.618+770G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689779 | ||||||
chr18:689818
|
C | T | 174 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0309others(171): Show | 183 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.618+731G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689818 | ||||||
chr18:689843
|
A | G | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.618+706T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689843 | ||||||
chr18:689845
|
AGGCATGA others(486): Show |
A | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.618+211_618+703del | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689845 | ||||||
chr18:689854
|
T | G | 135 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(132): Show | 142 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.618+695A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 689854 | ||||||
chr18:690207
|
G | A | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+342C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690207 | ||||||
chr18:690230
|
T | G | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.618+319A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690230 | ||||||
chr18:690297
|
T | C | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.618+252A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690297 | ||||||
chr18:690339
|
T | C | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.618+210A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690339 | ||||||
chr18:690346
|
T | C | 1 | a0001c0001t0034g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.618+203A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690346 | ||||||
chr18:690436
|
C | T | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.618+113G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690436 | ||||||
chr18:690460
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.618+89C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690460 | ||||||
chr18:690521
|
G | A | 1 | a0003c0007t0002g0353 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.618+28C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 8/15 | chr18 | 690521 | ||||||
chr18:690656
|
A | G | 7 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.536-25T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690656 | ||||||
chr18:690702
|
A | AAGCTGTT others(15): Show |
172 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(169): Show | 181 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.536-93_536-72dupGG others(20): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690702 | ||||||
chr18:690702
|
A | AAGCTGTT others(37): Show |
1 | a0001c0001t0002g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.536-72_536-71insGG others(42): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690702 | ||||||
chr18:690734
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0180 | 2 | HG00642.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.536-103G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690734 | ||||||
chr18:690781
|
G | A | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.536-150C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690781 | ||||||
chr18:690810
|
C | T | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.536-179G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 7/15 | chr18 | 690810 | ||||||
chr18:691117
|
T | C | 2 | a0001c0003t0001g0285a0001c0003t0001g0314 | 2 | NA18968.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.497-11A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 6/15 | chr18 | 691117 | ||||||
chr18:691173
|
G | A | 277 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(274): Show | 289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.496+31C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 6/15 | chr18 | 691173 | ||||||
chr18:691305
|
C | G | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-29G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691305 | ||||||
chr18:691439
|
T | C | 279 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(276): Show | 291 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.424-163A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691439 | ||||||
chr18:691484
|
T | A | 1 | a0002c0002t0002g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424-208A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691484 | ||||||
chr18:691485
|
C | G | 1 | a0002c0002t0002g0193 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.424-209G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691485 | ||||||
chr18:691507
|
G | A | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.424-231C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691507 | ||||||
chr18:691682
|
T | A | 1 | a0001c0001t0020g0236 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.424-406A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691682 | ||||||
chr18:691780
|
A | G | 95 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(92): Show | 98 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.424-504T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691780 | ||||||
chr18:691890
|
T | C | 92 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(89): Show | 95 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.424-614A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691890 | ||||||
chr18:691927
|
C | T | 14 | a0002c0002t0006g0147a0002c0002t0011g0058a0002c0002t0011g0103others(11): Show | 14 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.424-651G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691927 | ||||||
chr18:691968
|
A | G | 1 | a0003c0004t0003g0383 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.424-692T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 691968 | ||||||
chr18:692066
|
C | A | 4 | a0002c0002t0002g0098a0002c0002t0005g0135a0002c0002t0005g0177others(1): Show | 4 | HG01496.hp1 HG02738.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-790G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692066 | ||||||
chr18:692082
|
G | A | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.424-806C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692082 | ||||||
chr18:692095
|
A | G | 277 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(274): Show | 289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.424-819T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692095 | ||||||
chr18:692107
|
T | C | 128 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(125): Show | 135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.424-831A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692107 | ||||||
chr18:692118
|
T | C | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.424-842A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692118 | ||||||
chr18:692152
|
T | C | 81 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(78): Show | 84 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.424-876A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692152 | ||||||
chr18:692154
|
C | T | 1 | a0003c0007t0002g0378 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.424-878G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692154 | ||||||
chr18:692183
|
C | T | 119 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(116): Show | 123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.424-907G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692183 | ||||||
chr18:692233
|
T | C | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.424-957A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692233 | ||||||
chr18:692238
|
T | A | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.424-962A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692238 | ||||||
chr18:692251
|
A | G | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-975T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692251 | ||||||
chr18:692282
|
T | G | 173 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(170): Show | 182 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.424-1006A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692282 | ||||||
chr18:692397
|
C | T | 2 | a0001c0001t0010g0317a0003c0007t0010g0397 | 2 | HG00140.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.424-1121G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692397 | ||||||
chr18:692517
|
A | G | 1 | a0001c0001t0038g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.424-1241T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692517 | ||||||
chr18:692596
|
T | TA | 28 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(25): Show | 29 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.423+1285dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692596 | ||||||
chr18:692596
|
TA | T | 15 | a0001c0001t0001g0246a0001c0001t0001g0328a0001c0001t0002g0043others(12): Show | 15 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.423+1285delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692596 | ||||||
chr18:692629
|
AAAAAG | A | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.423+1248_423+1252d others(7): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692629 | ||||||
chr18:692631
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.423+1251T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692631 | ||||||
chr18:692638
|
A | G | 1 | a0003c0004t0003g0347 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.423+1244T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692638 | ||||||
chr18:692808
|
C | T | 17 | a0001c0001t0001g0152a0001c0001t0006g0042a0001c0001t0006g0107others(14): Show | 17 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.423+1074G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692808 | ||||||
chr18:692817
|
A | T | 1 | a0002c0002t0004g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.423+1065T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692817 | ||||||
chr18:692889
|
A | G | 2 | a0003c0007t0002g0354a0003c0007t0002g0380 | 2 | NA18986.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.423+993T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692889 | ||||||
chr18:692891
|
C | A | 1 | a0006c0010t0002g0346 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.423+991G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692891 | ||||||
chr18:692928
|
CTT | C | 9 | a0001c0006t0004g0002a0001c0006t0004g0006a0001c0006t0004g0148others(6): Show | 12 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.423+952_423+953del others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692928 | ||||||
chr18:692998
|
C | T | 2 | a0001c0001t0002g0115a0001c0001t0002g0166 | 2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.423+884G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 692998 | ||||||
chr18:693073
|
G | A | 1 | a0001c0003t0001g0249 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.423+809C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693073 | ||||||
chr18:693112
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.423+770C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693112 | ||||||
chr18:693266
|
T | C | 1 | a0001c0001t0035g0109 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.423+616A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693266 | ||||||
chr18:693269
|
A | C | 82 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(79): Show | 85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.423+613T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693269 | ||||||
chr18:693285
|
A | T | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.423+597T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693285 | ||||||
chr18:693673
|
C | T | 1 | a0002c0002t0005g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.423+209G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693673 | ||||||
chr18:693674
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.423+208G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693674 | ||||||
chr18:693763
|
T | C | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.423+119A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693763 | ||||||
chr18:693767
|
C | T | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.423+115G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693767 | ||||||
chr18:693826
|
T | A | 14 | a0002c0002t0006g0147a0002c0002t0011g0058a0002c0002t0011g0103others(11): Show | 14 | HG01884.hp1 HG02486.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.423+56A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693826 | ||||||
chr18:693828
|
A | C | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.423+54T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 5/15 | chr18 | 693828 | ||||||
chr18:693931
|
T | C | 1 | a0004c0008t0001g0386 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.397-23A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693931 | ||||||
chr18:693940
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.397-32T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693940 | ||||||
chr18:693943
|
T | C | 1 | a0001c0001t0038g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.397-35A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693943 | ||||||
chr18:693977
|
G | A | 191 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(188): Show | 200 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.397-69C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693977 | ||||||
chr18:693986
|
GCT | G | 278 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(275): Show | 290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.397-80_397-79delAG | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 693986 | ||||||
chr18:694192
|
A | G | 1 | a0001c0001t0010g0318 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.396+56T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 694192 | ||||||
chr18:694206
|
A | G | 282 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(279): Show | 294 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.396+42T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 4/15 | chr18 | 694206 | ||||||
chr18:694538
|
G | A | 42 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(39): Show | 44 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.310-204C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694538 | ||||||
chr18:694568
|
C | T | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.310-234G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694568 | ||||||
chr18:694600
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.310-266G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694600 | ||||||
chr18:694627
|
C | CA | 21 | a0001c0001t0001g0152a0001c0001t0002g0028a0001c0001t0002g0076others(18): Show | 21 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.310-294dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694627 | ||||||
chr18:694635
|
A | C | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.310-301T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694635 | ||||||
chr18:694653
|
G | A | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.310-319C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694653 | ||||||
chr18:694678
|
G | A | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.310-344C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694678 | ||||||
chr18:694703
|
T | C | 87 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(84): Show | 90 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.310-369A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694703 | ||||||
chr18:694784
|
A | T | 1 | a0001c0006t0004g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.310-450T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694784 | ||||||
chr18:694808
|
T | TTCTC | 57 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(54): Show | 59 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.310-478_310-475dup others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694808 | ||||||
chr18:694818
|
C | A | 16 | a0001c0001t0001g0152a0001c0001t0006g0042a0001c0001t0006g0153others(13): Show | 16 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.310-484G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694818 | ||||||
chr18:694818
|
C | CTCTA | 26 | a0002c0002t0002g0319a0002c0002t0004g0024a0002c0002t0004g0025others(23): Show | 27 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.310-485_310-484ins others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694818 | ||||||
chr18:694868
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.310-534A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694868 | ||||||
chr18:694902
|
G | C | 1 | a0003c0007t0003g0361 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.310-568C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 694902 | ||||||
chr18:695030
|
G | A | 58 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(55): Show | 60 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.310-696C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695030 | ||||||
chr18:695105
|
C | G | 1 | a0001c0001t0002g0167 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.310-771G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695105 | ||||||
chr18:695136
|
C | A | 1 | a0001c0001t0002g0172 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.310-802G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695136 | ||||||
chr18:695252
|
T | G | 4 | a0001c0003t0001g0249a0001c0003t0001g0254a0001c0003t0001g0316others(1): Show | 4 | HG02015.hp1 NA18955.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.310-918A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695252 | ||||||
chr18:695297
|
G | A | 3 | a0001c0003t0001g0287a0001c0003t0001g0332a0001c0017t0001g0344 | 3 | NA18981.hp1 NA19005.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.310-963C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695297 | ||||||
chr18:695319
|
T | C | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.310-985A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695319 | ||||||
chr18:695322
|
T | C | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.310-988A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695322 | ||||||
chr18:695367
|
G | A | 58 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(55): Show | 60 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.310-1033C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695367 | ||||||
chr18:695467
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.310-1133G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695467 | ||||||
chr18:695558
|
A | ATGG | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.310-1227_310-1225d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695558 | ||||||
chr18:695738
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.310-1404G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695738 | ||||||
chr18:695959
|
T | C | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.309+1281A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695959 | ||||||
chr18:695980
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.309+1260G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695980 | ||||||
chr18:695981
|
G | A | 1 | a0003c0007t0002g0353 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.309+1259C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 695981 | ||||||
chr18:696082
|
T | C | 1 | a0003c0004t0002g0358 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.309+1158A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696082 | ||||||
chr18:696204
|
C | CT | 12 | a0001c0001t0001g0053a0001c0001t0001g0271a0001c0001t0001g0277others(9): Show | 12 | HG01358.hp1 HG01516.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.309+1035dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | ||||||
chr18:696204
|
C | CTT | 161 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0004others(158): Show | 170 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.309+1034_309+1035d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | ||||||
chr18:696204
|
C | CTTT | 12 | a0001c0001t0001g0152a0001c0001t0002g0028a0001c0001t0002g0082others(9): Show | 12 | HG00673.hp1 HG02622.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.309+1033_309+1035d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | ||||||
chr18:696204
|
CTT | C | 82 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(79): Show | 85 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.309+1034_309+1035d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | ||||||
chr18:696204
|
CTTTTTTT others(3): Show |
C | 6 | a0001c0001t0002g0027a0001c0001t0002g0034a0001c0001t0002g0048others(3): Show | 6 | NA18941.hp1 NA18984.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1026_309+1035d others(12): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696204 | ||||||
chr18:696254
|
C | G | 1 | a0001c0001t0001g0108 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.309+986G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696254 | ||||||
chr18:696274
|
C | T | 1 | a0001c0001t0038g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.309+966G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696274 | ||||||
chr18:696302
|
C | G | 1 | a0001c0001t0002g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.309+938G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696302 | ||||||
chr18:696313
|
G | A | 1 | a0002c0002t0031g0337 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.309+927C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696313 | ||||||
chr18:696360
|
C | T | 1 | a0002c0002t0005g0177 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.309+880G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696360 | ||||||
chr18:696401
|
C | T | 1 | a0006c0010t0029g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309+839G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696401 | ||||||
chr18:696451
|
T | C | 1 | a0001c0001t0012g0041 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.309+789A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696451 | ||||||
chr18:696478
|
T | C | 4 | a0003c0004t0001g0399a0003c0004t0003g0350a0003c0004t0003g0377others(1): Show | 4 | HG00544.hp2 NA18747.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+762A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696478 | ||||||
chr18:696501
|
G | A | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.309+739C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696501 | ||||||
chr18:696502
|
C | T | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.309+738G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696502 | ||||||
chr18:696533
|
C | T | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.309+707G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696533 | ||||||
chr18:696583
|
C | A | 8 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.309+657G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696583 | ||||||
chr18:696645
|
T | C | 86 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(83): Show | 89 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.309+595A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696645 | ||||||
chr18:696667
|
C | T | 3 | a0004c0008t0001g0367a0004c0008t0001g0368a0004c0008t0001g0386 | 3 | HG01257.hp2 HG01258.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.309+573G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696667 | ||||||
chr18:696703
|
A | G | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.309+537T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696703 | ||||||
chr18:696748
|
T | C | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.309+492A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696748 | ||||||
chr18:696842
|
C | A | 2 | a0002c0002t0005g0289a0002c0002t0005g0290 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.309+398G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696842 | ||||||
chr18:696892
|
G | A | 9 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.309+348C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696892 | ||||||
chr18:696915
|
G | A | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.309+325C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696915 | ||||||
chr18:696933
|
G | A | 1 | a0002c0002t0004g0024 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.309+307C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 696933 | ||||||
chr18:697049
|
G | A | 3 | a0001c0001t0002g0127a0001c0001t0002g0129a0001c0001t0002g0172 | 3 | HG03490.hp2 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.309+191C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697049 | ||||||
chr18:697065
|
C | T | 17 | a0001c0001t0001g0152a0001c0001t0006g0042a0001c0001t0006g0107others(14): Show | 17 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.309+175G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697065 | ||||||
chr18:697066
|
A | G | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.309+174T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697066 | ||||||
chr18:697123
|
TAAATAAA others(5): Show |
T | 2 | a0001c0001t0002g0171a0001c0001t0002g0229 | 2 | HG01167.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.309+105_309+116del others(12): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697123 | ||||||
chr18:697147
|
C | T | 1 | a0001c0003t0001g0293 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.309+93G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 3/15 | chr18 | 697147 | ||||||
chr18:697377
|
CTT | C | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.194-24_194-23delAA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697377 | ||||||
chr18:697622
|
G | A | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.194-267C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697622 | ||||||
chr18:697699
|
C | T | 1 | a0001c0003t0001g0269 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.194-344G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697699 | ||||||
chr18:697857
|
T | C | 179 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(176): Show | 185 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.194-502A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697857 | ||||||
chr18:697912
|
G | A | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.194-557C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697912 | ||||||
chr18:697922
|
A | G | 87 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(84): Show | 90 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.194-567T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697922 | ||||||
chr18:697927
|
A | G | 87 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(84): Show | 90 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.194-572T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697927 | ||||||
chr18:697938
|
C | A | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.194-583G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697938 | ||||||
chr18:697943
|
G | A | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.194-588C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697943 | ||||||
chr18:697945
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.194-590G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 697945 | ||||||
chr18:698024
|
G | A | 118 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(115): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(119): Show |
intron_variant | MODIFIER | c.194-669C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698024 | ||||||
chr18:698225
|
T | C | 1 | a0001c0001t0034g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.194-870A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698225 | ||||||
chr18:698227
|
G | A | 1 | a0001c0003t0001g0291 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.194-872C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698227 | ||||||
chr18:698311
|
C | T | 21 | a0002c0002t0001g0099a0002c0002t0002g0231a0002c0002t0005g0178others(18): Show | 22 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.194-956G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698311 | ||||||
chr18:698312
|
A | G | 87 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(84): Show | 90 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.194-957T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698312 | ||||||
chr18:698491
|
T | C | 7 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.194-1136A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698491 | ||||||
chr18:698589
|
G | A | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.194-1234C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698589 | ||||||
chr18:698624
|
A | AATTATT | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.194-1275_194-1270d others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698624 | ||||||
chr18:698696
|
T | C | 2 | a0001c0001t0017g0077a0001c0001t0017g0205 | 2 | NA18995.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.194-1341A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698696 | ||||||
chr18:698738
|
C | T | 1 | a0006c0010t0029g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.194-1383G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 698738 | ||||||
chr18:699120
|
G | T | 83 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.194-1765C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699120 | ||||||
chr18:699281
|
G | A | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.194-1926C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699281 | ||||||
chr18:699478
|
A | AAAT | 9 | a0001c0001t0001g0055a0001c0001t0001g0180a0001c0001t0001g0255others(6): Show | 9 | HG00642.hp1 HG01074.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.194-2126_194-2124d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | ||||||
chr18:699478
|
A | AAATAATA others(11): Show |
2 | a0002c0002t0009g0026a0002c0015t0002g0260 | 2 | HG02055.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.194-2141_194-2124d others(20): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | ||||||
chr18:699478
|
A | AAATAATA others(14): Show |
1 | a0009c0014t0027g0156 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.194-2144_194-2124d others(23): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | ||||||
chr18:699478
|
AAAT | A | 83 | a0002c0002t0001g0099a0002c0002t0002g0098a0002c0002t0002g0193others(80): Show | 86 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.194-2126_194-2124d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | ||||||
chr18:699478
|
AAATAAT | A | 190 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(187): Show | 199 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.194-2129_194-2124d others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699478 | ||||||
chr18:699530
|
A | T | 1 | a0001c0003t0001g0330 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.194-2175T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699530 | ||||||
chr18:699755
|
G | A | 1 | a0002c0002t0004g0056 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.194-2400C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699755 | ||||||
chr18:699805
|
C | A | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-2450G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699805 | ||||||
chr18:699881
|
A | G | 84 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(81): Show | 87 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.194-2526T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 699881 | ||||||
chr18:700039
|
C | A | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.194-2684G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700039 | ||||||
chr18:700041
|
T | C | 1 | a0001c0003t0001g0341 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.194-2686A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700041 | ||||||
chr18:700086
|
A | G | 2 | a0002c0002t0009g0093a0002c0002t0009g0133 | 2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.194-2731T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700086 | ||||||
chr18:700612
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.194-3257G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700612 | ||||||
chr18:700687
|
T | C | 277 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(274): Show | 289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.194-3332A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700687 | ||||||
chr18:700878
|
G | A | 57 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(54): Show | 59 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.194-3523C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700878 | ||||||
chr18:700890
|
C | CA | 65 | a0001c0001t0001g0189a0001c0001t0001g0217a0001c0001t0001g0222others(62): Show | 67 | HG00280.hp1 HG00639.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.194-3536dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | ||||||
chr18:700890
|
C | CAA | 28 | a0001c0001t0006g0042a0001c0001t0006g0153a0001c0001t0006g0154others(25): Show | 28 | HG00642.hp2 HG00673.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.194-3537_194-3536d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | ||||||
chr18:700890
|
CA | C | 109 | a0001c0001t0001g0084a0001c0001t0002g0001a0001c0001t0002g0016others(106): Show | 115 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.194-3536delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | ||||||
chr18:700890
|
CAA | C | 16 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(13): Show | 17 | HG00438.hp2 HG01261.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.194-3537_194-3536d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | ||||||
chr18:700890
|
CAAA | C | 34 | a0001c0001t0038g0335a0003c0004t0002g0358a0003c0004t0002g0395others(31): Show | 36 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.194-3538_194-3536d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700890 | ||||||
chr18:700916
|
A | G | 278 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(275): Show | 290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.194-3561T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700916 | ||||||
chr18:700951
|
G | T | 2 | a0001c0001t0020g0191a0001c0001t0020g0236 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.194-3596C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 700951 | ||||||
chr18:701022
|
A | G | 1 | a0003c0004t0004g0357 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.194-3667T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701022 | ||||||
chr18:701192
|
A | G | 7 | a0001c0001t0008g0007a0001c0001t0008g0216a0001c0001t0008g0218others(4): Show | 8 | NA18948.hp1 NA18969.hp2 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.194-3837T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701192 | ||||||
chr18:701193
|
T | G | 1 | a0001c0001t0008g0242 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.194-3838A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701193 | ||||||
chr18:701219
|
A | G | 1 | a0003c0004t0002g0395 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.194-3864T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701219 | ||||||
chr18:701464
|
A | AC | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.194-4110_194-4109i others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701464 | ||||||
chr18:701572
|
T | C | 276 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(273): Show | 288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.194-4217A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701572 | ||||||
chr18:701598
|
T | A | 1 | a0001c0001t0002g0112 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.194-4243A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701598 | ||||||
chr18:701749
|
T | C | 5 | a0002c0002t0013g0018a0002c0002t0013g0087a0002c0002t0013g0130others(2): Show | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.194-4394A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701749 | ||||||
chr18:701752
|
A | G | 95 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(92): Show | 98 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.194-4397T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701752 | ||||||
chr18:701756
|
C | CAA | 85 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0234others(82): Show | 88 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.194-4403_194-4402d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701756 | ||||||
chr18:701756
|
CA | C | 191 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(188): Show | 200 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.194-4402delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701756 | ||||||
chr18:701780
|
C | T | 1 | a0001c0006t0004g0235 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.194-4425G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701780 | ||||||
chr18:701939
|
G | GATAA | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+4527_193+4530d others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701939 | ||||||
chr18:701939
|
G | GATAAATA others(1): Show |
35 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0234others(32): Show | 36 | HG00408.hp2 HG00621.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.193+4523_193+4530d others(10): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701939 | ||||||
chr18:701939
|
G | GATAAATA others(5): Show |
10 | a0002c0002t0006g0147a0002c0002t0011g0058a0002c0002t0011g0103others(7): Show | 10 | HG01192.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+4519_193+4530d others(14): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 701939 | ||||||
chr18:702014
|
G | A | 279 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(276): Show | 291 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.193+4456C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702014 | ||||||
chr18:702077
|
A | G | 43 | a0001c0013t0002g0146a0003c0004t0001g0399a0003c0004t0002g0358others(40): Show | 45 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.193+4393T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702077 | ||||||
chr18:702098
|
T | C | 87 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0234others(84): Show | 90 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.193+4372A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702098 | ||||||
chr18:702196
|
T | G | 276 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(273): Show | 288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.193+4274A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702196 | ||||||
chr18:702217
|
T | C | 87 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0234others(84): Show | 90 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.193+4253A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702217 | ||||||
chr18:702264
|
C | CA | 72 | a0001c0001t0001g0252a0001c0003t0001g0139a0001c0003t0001g0234others(69): Show | 74 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.193+4205dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702264 | ||||||
chr18:702264
|
C | CAA | 16 | a0001c0003t0001g0138a0002c0002t0002g0193a0002c0002t0004g0024others(13): Show | 17 | HG01074.hp2 HG01123.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.193+4204_193+4205d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702264 | ||||||
chr18:702264
|
CA | C | 163 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(160): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.193+4205delT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702264 | ||||||
chr18:702264
|
CAA | C | 118 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(115): Show | 122 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.193+4204_193+4205d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702264 | ||||||
chr18:702439
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.193+4031C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702439 | ||||||
chr18:702512
|
C | T | 276 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(273): Show | 288 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.193+3958G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702512 | ||||||
chr18:702617
|
G | A | 98 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(95): Show | 102 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.193+3853C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702617 | ||||||
chr18:702632
|
C | T | 5 | a0002c0002t0013g0018a0002c0002t0013g0087a0002c0002t0013g0130others(2): Show | 5 | HG02809.hp1 HG03041.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+3838G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702632 | ||||||
chr18:702656
|
T | C | 1 | a0002c0002t0031g0337 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.193+3814A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702656 | ||||||
chr18:702862
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.193+3608T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702862 | ||||||
chr18:702993
|
G | C | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.193+3477C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 702993 | ||||||
chr18:703032
|
T | A | 1 | a0002c0002t0013g0130 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.193+3438A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703032 | ||||||
chr18:703062
|
T | C | 1 | a0001c0001t0012g0192 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.193+3408A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703062 | ||||||
chr18:703087
|
G | A | 9 | a0003c0004t0003g0013a0003c0004t0003g0348a0003c0004t0003g0359others(6): Show | 10 | HG00438.hp2 HG00621.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.193+3383C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703087 | ||||||
chr18:703185
|
G | A | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+3285C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703185 | ||||||
chr18:703216
|
G | A | 2 | a0001c0003t0001g0287a0001c0003t0001g0332 | 2 | NA18981.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.193+3254C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703216 | ||||||
chr18:703302
|
T | C | 1 | a0001c0003t0001g0291 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.193+3168A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703302 | ||||||
chr18:703388
|
AT | A | 277 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(274): Show | 289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.193+3081delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703388 | ||||||
chr18:703442
|
G | A | 277 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0001g0152others(274): Show | 289 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.193+3028C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703442 | ||||||
chr18:703446
|
G | T | 1 | a0002c0002t0002g0098 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.193+3024C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703446 | ||||||
chr18:703472
|
A | G | 1 | a0001c0001t0002g0198 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193+2998T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703472 | ||||||
chr18:703544
|
T | A | 1 | a0001c0003t0007g0288 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.193+2926A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703544 | ||||||
chr18:703785
|
G | C | 282 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(279): Show | 294 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.193+2685C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703785 | ||||||
chr18:703853
|
T | G | 1 | a0001c0003t0001g0313 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.193+2617A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 703853 | ||||||
chr18:704120
|
C | T | 3 | a0002c0002t0009g0089a0002c0002t0009g0090a0002c0002t0031g0337 | 3 | HG02258.hp1 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.193+2350G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704120 | ||||||
chr18:704191
|
TGAGAGGC others(12): Show |
T | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.193+2260_193+2278d others(21): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704191 | ||||||
chr18:704232
|
G | A | 272 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(269): Show | 284 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.193+2238C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704232 | ||||||
chr18:704246
|
T | C | 203 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(200): Show | 212 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.193+2224A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704246 | ||||||
chr18:704262
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.193+2208A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704262 | ||||||
chr18:704381
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.193+2089A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704381 | ||||||
chr18:704407
|
A | G | 272 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(269): Show | 284 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.193+2063T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704407 | ||||||
chr18:704440
|
G | GA | 8 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(5): Show | 8 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.193+2029dupT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | ||||||
chr18:704440
|
G | GAAA | 6 | a0002c0002t0013g0018a0002c0002t0013g0087a0002c0002t0013g0130others(3): Show | 6 | HG01192.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.193+2027_193+2029d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | ||||||
chr18:704440
|
G | GAAAA | 88 | a0001c0001t0001g0055a0001c0001t0001g0180a0001c0001t0002g0057others(85): Show | 93 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.193+2026_193+2029d others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | ||||||
chr18:704440
|
G | GAAAAA | 109 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(106): Show | 113 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.193+2025_193+2029d others(7): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | ||||||
chr18:704440
|
G | GAAAAAA | 52 | a0001c0001t0002g0048a0001c0001t0002g0054a0001c0001t0002g0072others(49): Show | 55 | HG00423.hp1 HG01074.hp2 HG01257.hp2 others(52): Show |
intron_variant | MODIFIER | c.193+2024_193+2029d others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | ||||||
chr18:704440
|
G | GAAAAAAA | 14 | a0001c0001t0001g0152a0001c0001t0002g0083a0001c0001t0006g0225others(11): Show | 14 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.193+2023_193+2029d others(9): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704440 | ||||||
chr18:704444
|
A | G | 2 | a0001c0001t0020g0191a0001c0001t0020g0236 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.193+2026T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704444 | ||||||
chr18:704535
|
T | C | 1 | a0001c0001t0038g0335 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193+1935A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704535 | ||||||
chr18:704569
|
G | T | 25 | a0001c0001t0001g0055a0001c0001t0001g0180a0001c0003t0001g0138others(22): Show | 25 | HG00408.hp2 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.193+1901C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704569 | ||||||
chr18:704578
|
T | C | 1 | a0002c0002t0021g0184 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.193+1892A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704578 | ||||||
chr18:704605
|
C | CT | 172 | a0001c0001t0001g0053a0001c0001t0001g0084a0001c0001t0002g0001others(169): Show | 181 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.193+1864dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704605 | ||||||
chr18:704605
|
C | CTT | 30 | a0001c0001t0001g0055a0001c0001t0001g0180a0001c0001t0002g0029others(27): Show | 30 | HG00438.hp1 HG00597.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.193+1863_193+1864d others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704605 | ||||||
chr18:704605
|
C | CTTT | 8 | a0001c0001t0002g0072a0001c0001t0002g0116a0001c0003t0001g0138others(5): Show | 8 | HG00408.hp2 HG02155.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+1862_193+1864d others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704605 | ||||||
chr18:704611
|
TC | T | 10 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(7): Show | 10 | HG00423.hp1 HG01109.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.193+1858delG | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704611 | ||||||
chr18:704612
|
C | T | 261 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(258): Show | 273 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(270): Show |
intron_variant | MODIFIER | c.193+1858G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704612 | ||||||
chr18:704667
|
G | A | 1 | a0005c0009t0001g0190 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.193+1803C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704667 | ||||||
chr18:704699
|
A | C | 1 | a0002c0002t0005g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.193+1771T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704699 | ||||||
chr18:704804
|
C | G | 208 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(205): Show | 217 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.193+1666G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704804 | ||||||
chr18:704825
|
T | C | 208 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(205): Show | 217 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.193+1645A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704825 | ||||||
chr18:704826
|
G | A | 20 | a0002c0002t0001g0099a0002c0002t0002g0231a0002c0002t0005g0178others(17): Show | 21 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.193+1644C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704826 | ||||||
chr18:704853
|
G | A | 1 | a0002c0002t0004g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.193+1617C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704853 | ||||||
chr18:704901
|
T | C | 271 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(268): Show | 283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.193+1569A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704901 | ||||||
chr18:704935
|
G | A | 1 | a0002c0002t0024g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193+1535C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704935 | ||||||
chr18:704955
|
C | CAGG | 278 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(275): Show | 290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.193+1514_193+1515i others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 704955 | ||||||
chr18:705087
|
C | T | 271 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(268): Show | 283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.193+1383G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705087 | ||||||
chr18:705147
|
G | A | 1 | a0004c0008t0004g0011 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.193+1323C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705147 | ||||||
chr18:705173
|
G | A | 1 | a0002c0005t0001g0019 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.193+1297C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705173 | ||||||
chr18:705257
|
C | A | 1 | a0002c0002t0024g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193+1213G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705257 | ||||||
chr18:705361
|
AT | A | 7 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(4): Show | 7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+1108delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705361 | ||||||
chr18:705489
|
C | T | 8 | a0001c0001t0034g0105a0002c0002t0011g0058a0002c0002t0011g0103others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.193+981G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705489 | ||||||
chr18:705519
|
C | T | 25 | a0001c0001t0001g0055a0001c0001t0001g0180a0001c0003t0001g0138others(22): Show | 25 | HG00408.hp2 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.193+951G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705519 | ||||||
chr18:705537
|
T | C | 1 | a0003c0004t0003g0371 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.193+933A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705537 | ||||||
chr18:705550
|
CTGTT | C | 7 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+916_193+919del others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705550 | ||||||
chr18:705598
|
T | C | 345 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(342): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.193+872A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705598 | ||||||
chr18:705648
|
G | A | 1 | a0002c0002t0024g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193+822C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705648 | ||||||
chr18:705658
|
G | A | 56 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(53): Show | 59 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.193+812C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705658 | ||||||
chr18:705686
|
T | C | 1 | a0001c0001t0002g0057 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.193+784A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705686 | ||||||
chr18:705695
|
G | T | 271 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(268): Show | 283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.193+775C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705695 | ||||||
chr18:705753
|
A | G | 5 | a0001c0001t0001g0188a0001c0001t0001g0215a0001c0001t0001g0263others(2): Show | 5 | HG00558.hp2 HG00597.hp2 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.193+717T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705753 | ||||||
chr18:705755
|
T | C | 7 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.193+715A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705755 | ||||||
chr18:705788
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.193+682G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705788 | ||||||
chr18:705820
|
T | C | 271 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(268): Show | 283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.193+650A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705820 | ||||||
chr18:705996
|
G | C | 1 | a0001c0001t0002g0054 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.193+474C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 705996 | ||||||
chr18:706047
|
G | T | 278 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(275): Show | 290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.193+423C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706047 | ||||||
chr18:706092
|
G | A | 46 | a0001c0013t0002g0146a0003c0004t0001g0399a0003c0004t0002g0358others(43): Show | 49 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.193+378C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706092 | ||||||
chr18:706125
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.193+345G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706125 | ||||||
chr18:706182
|
T | C | 271 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(268): Show | 283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.193+288A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706182 | ||||||
chr18:706183
|
C | T | 207 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(204): Show | 216 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.193+287G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706183 | ||||||
chr18:706187
|
G | T | 1 | a0001c0001t0010g0257 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.193+283C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706187 | ||||||
chr18:706206
|
G | A | 56 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(53): Show | 59 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.193+264C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706206 | ||||||
chr18:706322
|
C | CACTG | 271 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(268): Show | 283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.193+147_193+148ins others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706322 | ||||||
chr18:706348
|
A | T | 2 | a0002c0002t0009g0026a0009c0014t0027g0156 | 2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.193+122T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706348 | ||||||
chr18:706450
|
C | T | 1 | a0002c0002t0024g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.193+20G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 2/15 | chr18 | 706450 | ||||||
chr18:706589
|
A | G | 278 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(275): Show | 290 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.85-11T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706589 | ||||||
chr18:706626
|
C | T | 1 | a0003c0004t0003g0384 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.85-48G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706626 | ||||||
chr18:706801
|
G | GTATA | 3 | a0002c0002t0009g0026a0002c0015t0002g0260a0009c0014t0027g0156 | 3 | HG02055.hp2 HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.85-227_85-224dupTA others(2): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | ||||||
chr18:706801
|
G | GTATATAT others(1): Show |
13 | a0001c0001t0001g0084a0001c0001t0002g0017a0001c0001t0002g0036others(10): Show | 13 | HG00741.hp1 HG01106.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.85-231_85-224dupTA others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | ||||||
chr18:706801
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0002g0126 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.85-233_85-224dupTA others(8): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | ||||||
chr18:706801
|
G | GTGTATA | 7 | a0003c0004t0003g0356a0003c0004t0003g0366a0003c0004t0003g0372others(4): Show | 7 | HG01257.hp2 HG01258.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-224_85-223insTA others(4): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | ||||||
chr18:706801
|
G | GTGTATAT others(1): Show |
16 | a0003c0004t0003g0013a0003c0004t0003g0347a0003c0004t0003g0348others(13): Show | 17 | HG00423.hp1 HG02004.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.85-224_85-223insTA others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706801 | ||||||
chr18:706803
|
A | G | 38 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(35): Show | 40 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.85-225T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706803 | ||||||
chr18:706810
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-232A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706810 | ||||||
chr18:706812
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-234A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706812 | ||||||
chr18:706813
|
A | G | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-235T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706813 | ||||||
chr18:706813
|
A | T | 1 | a0003c0007t0010g0397 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.85-235T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706813 | ||||||
chr18:706814
|
T | A | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-236A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706814 | ||||||
chr18:706815
|
A | ATATAT | 8 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-238_85-237insAT others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | ATATATAT | 80 | a0001c0001t0001g0180a0001c0001t0002g0001a0001c0001t0002g0004others(77): Show | 84 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.85-238_85-237insAT others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | ATATATAT others(2): Show |
7 | a0001c0001t0001g0053a0001c0001t0002g0052a0001c0001t0002g0054others(4): Show | 7 | HG01516.hp2 HG02300.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.85-238_85-237insAT others(7): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | ATATATAT others(4): Show |
1 | a0001c0006t0004g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.85-238_85-237insAT others(9): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | ATATATAT others(4): Show |
1 | a0002c0002t0006g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.85-238_85-237insAA others(9): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | ATATATAT others(1): Show |
22 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0029others(19): Show | 22 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.85-238_85-237insAA others(6): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | ATATATTT | 10 | a0001c0001t0002g0164a0001c0001t0002g0199a0001c0013t0002g0146others(7): Show | 11 | HG01074.hp2 HG01261.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.85-238_85-237insAA others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | ATATTT | 6 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-238_85-237insAA others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | C | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-237T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
A | T | 47 | a0001c0001t0001g0188a0001c0001t0001g0215a0001c0001t0001g0217others(44): Show | 49 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.85-237T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706815
|
AT | A | 9 | a0001c0001t0001g0252a0001c0001t0020g0191a0001c0001t0020g0236others(6): Show | 9 | HG00673.hp2 HG01361.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.85-238delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706815 | ||||||
chr18:706816
|
T | A | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-238A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | ||||||
chr18:706816
|
T | TA | 6 | a0001c0001t0001g0222a0001c0001t0001g0255a0001c0001t0001g0292others(3): Show | 6 | HG00639.hp2 HG01074.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-239_85-238insT | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | ||||||
chr18:706816
|
T | TATATA | 7 | a0002c0002t0005g0186a0002c0002t0013g0018a0002c0002t0013g0087others(4): Show | 7 | HG02809.hp1 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-239_85-238insTA others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | ||||||
chr18:706816
|
T | TATATATA | 69 | a0001c0001t0001g0055a0001c0001t0002g0037a0001c0001t0002g0127others(66): Show | 71 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.85-239_85-238insTA others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | ||||||
chr18:706816
|
T | TATATATA others(2): Show |
3 | a0001c0001t0034g0105a0002c0002t0024g0061a0003c0004t0003g0374 | 3 | HG02523.hp2 HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.85-239_85-238insTA others(7): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | ||||||
chr18:706816
|
T | TATATATA others(4): Show |
4 | a0001c0006t0004g0002a0001c0006t0004g0148a0001c0006t0004g0235others(1): Show | 6 | HG01496.hp1 HG01891.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-239_85-238insTA others(9): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | ||||||
chr18:706816
|
T | TATATATA others(6): Show |
5 | a0001c0006t0004g0006a0001c0006t0004g0149a0001c0006t0004g0237others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.85-239_85-238insTA others(11): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706816 | ||||||
chr18:706817
|
T | A | 16 | a0001c0001t0001g0342a0001c0001t0002g0086a0001c0001t0002g0163others(13): Show | 16 | HG00741.hp1 HG01106.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.85-239A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706817 | ||||||
chr18:706817
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-239A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706817 | ||||||
chr18:706818
|
T | A | 48 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(45): Show | 50 | HG00280.hp1 HG00408.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.85-240A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706818 | ||||||
chr18:706818
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-240A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706818 | ||||||
chr18:706819
|
T | A | 9 | a0001c0001t0001g0343a0001c0001t0006g0042a0001c0001t0006g0107others(6): Show | 9 | HG01106.hp1 HG01934.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.85-241A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706819 | ||||||
chr18:706820
|
T | A | 30 | a0002c0002t0001g0099a0002c0002t0002g0098a0002c0002t0002g0231others(27): Show | 31 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.85-242A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706820 | ||||||
chr18:706820
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-242A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706820 | ||||||
chr18:706821
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-243A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706821 | ||||||
chr18:706822
|
T | A | 2 | a0001c0001t0001g0343a0002c0005t0001g0064 | 2 | HG01934.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.85-244A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706822 | ||||||
chr18:706824
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.85-246A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706824 | ||||||
chr18:706944
|
G | A | 2 | a0001c0003t0001g0238a0001c0003t0001g0239 | 2 | NA18999.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.85-366C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706944 | ||||||
chr18:706957
|
T | C | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-379A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706957 | ||||||
chr18:706961
|
G | C | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-383C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706961 | ||||||
chr18:706962
|
G | T | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-384C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706962 | ||||||
chr18:706964
|
A | T | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-386T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706964 | ||||||
chr18:706965
|
C | T | 215 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(212): Show | 224 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.85-387G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706965 | ||||||
chr18:706966
|
G | A | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-388C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706966 | ||||||
chr18:706967
|
T | G | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-389A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706967 | ||||||
chr18:706968
|
G | A | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-390C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706968 | ||||||
chr18:706969
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-391G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706969 | ||||||
chr18:706970
|
C | T | 1 | a0001c0001t0001g0322 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.85-392G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 706970 | ||||||
chr18:707431
|
A | C | 3 | a0001c0003t0001g0241a0001c0003t0001g0262a0001c0003t0001g0301 | 3 | HG00673.hp2 NA18961.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.85-853T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707431 | ||||||
chr18:707470
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.85-892C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707470 | ||||||
chr18:707497
|
T | C | 271 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(268): Show | 283 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(280): Show |
intron_variant | MODIFIER | c.85-919A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707497 | ||||||
chr18:707511
|
G | C | 40 | a0002c0002t0001g0092a0002c0002t0001g0099a0002c0002t0002g0098others(37): Show | 42 | HG00280.hp1 HG00642.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.85-933C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707511 | ||||||
chr18:707560
|
A | C | 272 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(269): Show | 284 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(281): Show |
intron_variant | MODIFIER | c.85-982T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707560 | ||||||
chr18:707592
|
T | C | 1 | a0003c0004t0003g0375 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.85-1014A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707592 | ||||||
chr18:707637
|
A | G | 2 | a0001c0001t0001g0261a0001c0001t0014g0300 | 2 | HG00099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.85-1059T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707637 | ||||||
chr18:707732
|
GTTTAA | G | 56 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(53): Show | 59 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.85-1159_85-1155del others(5): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707732 | ||||||
chr18:707851
|
TTTA | T | 281 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(278): Show | 293 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.85-1276_85-1274del others(3): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 707851 | ||||||
chr18:708023
|
C | CT | 52 | a0001c0001t0002g0198a0001c0001t0007g0321a0001c0003t0001g0214others(49): Show | 55 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.85-1446dupA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708023 | ||||||
chr18:708023
|
CT | C | 194 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(191): Show | 203 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.85-1446delA | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708023 | ||||||
chr18:708063
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1485C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708063 | ||||||
chr18:708066
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1488C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708066 | ||||||
chr18:708068
|
C | T | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1490G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708068 | ||||||
chr18:708069
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1491G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708069 | ||||||
chr18:708071
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1493C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708071 | ||||||
chr18:708074
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1496A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708074 | ||||||
chr18:708075
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1497C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708075 | ||||||
chr18:708077
|
T | C | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1499A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708077 | ||||||
chr18:708078
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1500G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708078 | ||||||
chr18:708081
|
G | T | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1503C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708081 | ||||||
chr18:708082
|
A | T | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1504T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708082 | ||||||
chr18:708083
|
A | C | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1505T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708083 | ||||||
chr18:708085
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1507A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708085 | ||||||
chr18:708089
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1511C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708089 | ||||||
chr18:708093
|
T | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1515A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708093 | ||||||
chr18:708114
|
G | C | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1536C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708114 | ||||||
chr18:708136
|
C | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1558G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708136 | ||||||
chr18:708137
|
A | C | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1559T>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708137 | ||||||
chr18:708138
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1560C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708138 | ||||||
chr18:708150
|
C | CACGCCCA others(3): Show |
1 | a0001c0001t0002g0043 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.85-1573_85-1572ins others(10): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708150 | ||||||
chr18:708157
|
G | A | 7 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(4): Show | 7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.85-1579C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708157 | ||||||
chr18:708207
|
C | T | 6 | a0002c0002t0005g0178a0002c0002t0005g0179a0002c0005t0001g0063others(3): Show | 6 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.85-1629G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708207 | ||||||
chr18:708237
|
G | C | 1 | a0001c0001t0001g0334 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.85-1659C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708237 | ||||||
chr18:708299
|
T | C | 272 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(269): Show | 284 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.85-1721A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708299 | ||||||
chr18:708586
|
C | T | 1 | a0002c0002t0024g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.85-2008G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708586 | ||||||
chr18:708710
|
C | G | 273 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(270): Show | 285 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.85-2132G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 708710 | ||||||
chr18:709140
|
C | A | 1 | a0004c0008t0004g0398 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.85-2562G>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709140 | ||||||
chr18:709179
|
G | A | 8 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.85-2601C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709179 | ||||||
chr18:709202
|
G | A | 61 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(58): Show | 64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.85-2624C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709202 | ||||||
chr18:709232
|
C | T | 209 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(206): Show | 218 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.85-2654G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709232 | ||||||
chr18:709293
|
G | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0180a0001c0003t0001g0138others(22): Show | 25 | HG00408.hp2 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.85-2715C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709293 | ||||||
chr18:709379
|
A | G | 272 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(269): Show | 284 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.85-2801T>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709379 | ||||||
chr18:709396
|
G | A | 3 | a0002c0002t0025g0102a0002c0005t0001g0145a0002c0005t0001g0185 | 3 | HG01123.hp2 HG01192.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.85-2818C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709396 | ||||||
chr18:709590
|
G | T | 272 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(269): Show | 284 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.84+2914C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709590 | ||||||
chr18:709679
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.84+2825C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709679 | ||||||
chr18:709834
|
T | A | 1 | a0003c0004t0003g0376 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.84+2670A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709834 | ||||||
chr18:709950
|
C | T | 6 | a0002c0002t0011g0058a0002c0002t0011g0103a0002c0002t0011g0104others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.84+2554G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 709950 | ||||||
chr18:710143
|
C | T | 1 | a0003c0004t0003g0355 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.84+2361G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710143 | ||||||
chr18:710146
|
T | A | 60 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(57): Show | 63 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.84+2358A>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710146 | ||||||
chr18:710177
|
C | G | 1 | a0001c0001t0002g0197 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.84+2327G>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710177 | ||||||
chr18:710265
|
C | T | 59 | a0001c0001t0001g0152a0001c0001t0006g0225a0001c0001t0012g0040others(56): Show | 62 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.84+2239G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710265 | ||||||
chr18:710388
|
G | C | 4 | a0003c0004t0001g0399a0003c0004t0003g0350a0003c0004t0003g0377others(1): Show | 4 | HG00544.hp2 NA18747.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.84+2116C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710388 | ||||||
chr18:710534
|
G | T | 1 | a0002c0002t0005g0186 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.84+1970C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710534 | ||||||
chr18:710554
|
G | A | 7 | a0001c0001t0006g0042a0001c0001t0006g0107a0001c0001t0006g0153others(4): Show | 7 | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.84+1950C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710554 | ||||||
chr18:710560
|
G | A | 1 | a0003c0004t0003g0400 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.84+1944C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710560 | ||||||
chr18:710854
|
G | C | 1 | a0002c0002t0005g0212 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.84+1650C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710854 | ||||||
chr18:710883
|
T | C | 1 | a0002c0002t0025g0102 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.84+1621A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710883 | ||||||
chr18:710980
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.84+1524C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 710980 | ||||||
chr18:711017
|
G | A | 68 | a0001c0001t0001g0152a0001c0001t0006g0042a0001c0001t0006g0107others(65): Show | 71 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.84+1487C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711017 | ||||||
chr18:711066
|
A | T | 3 | a0001c0001t0002g0062a0001c0001t0002g0195a0001c0001t0002g0196 | 3 | HG03491.hp1 HG03492.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.84+1438T>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711066 | ||||||
chr18:711167
|
C | T | 8 | a0001c0001t0034g0105a0002c0002t0011g0058a0002c0002t0011g0103others(5): Show | 8 | HG01884.hp1 HG02486.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.84+1337G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711167 | ||||||
chr18:711334
|
T | C | 1 | a0001c0003t0001g0295 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.84+1170A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711334 | ||||||
chr18:711341
|
G | A | 69 | a0001c0001t0001g0152a0001c0001t0006g0042a0001c0001t0006g0107others(66): Show | 72 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.84+1163C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711341 | ||||||
chr18:711370
|
G | A | 1 | a0002c0002t0024g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.84+1134C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711370 | ||||||
chr18:711462
|
T | C | 14 | a0001c0006t0004g0002a0001c0006t0004g0006a0001c0006t0004g0148others(11): Show | 17 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.84+1042A>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711462 | ||||||
chr18:711559
|
G | C | 194 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(191): Show | 203 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.84+945C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711559 | ||||||
chr18:711845
|
G | C | 1 | a0001c0001t0016g0150 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.84+659C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711845 | ||||||
chr18:711919
|
C | T | 2 | a0001c0003t0001g0238a0001c0003t0001g0239 | 2 | NA18999.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.84+585G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 711919 | ||||||
chr18:712037
|
G | A | 195 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(192): Show | 204 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.84+467C>T | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712037 | ||||||
chr18:712263
|
T | G | 6 | a0001c0001t0001g0258a0001c0001t0010g0223a0001c0001t0010g0224others(3): Show | 6 | HG00741.hp2 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.84+241A>C | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712263 | ||||||
chr18:712319
|
TCGG | T | 275 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(272): Show | 287 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.84+182_84+184delCC others(1): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712319 | ||||||
chr18:712331
|
G | C | 1 | a0001c0001t0002g0187 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.84+173C>G | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712331 | ||||||
chr18:712349
|
G | GCCGCGCG others(11): Show |
1 | a0001c0003t0001g0259 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.84+137_84+154dupAC others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(11): Show |
11 | a0001c0001t0002g0227a0001c0001t0002g0228a0001c0001t0002g0229others(8): Show | 11 | HG00609.hp2 HG01891.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(29): Show |
22 | a0001c0001t0001g0194a0001c0001t0002g0195a0001c0001t0002g0196others(19): Show | 22 | HG00408.hp2 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(34): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(47): Show |
48 | a0001c0001t0001g0152a0001c0001t0001g0180a0001c0001t0002g0001others(45): Show | 52 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(52): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(65): Show |
64 | a0001c0001t0001g0108a0001c0001t0002g0004a0001c0001t0002g0110others(61): Show | 67 | HG00544.hp2 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(70): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(83): Show |
64 | a0001c0001t0001g0084a0001c0001t0002g0062a0001c0001t0002g0065others(61): Show | 68 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(65): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(88): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(101): Show |
27 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0002g0043others(24): Show | 27 | HG00558.hp1 HG00621.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(106): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(119): Show |
16 | a0001c0001t0002g0027a0001c0001t0002g0028a0001c0001t0002g0029others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(124): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(137): Show |
9 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0032g0020others(6): Show | 9 | HG00408.hp1 HG00544.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(142): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
G | GCCGCGCT others(155): Show |
5 | a0001c0001t0002g0016a0001c0001t0002g0017a0002c0002t0013g0018others(2): Show | 5 | HG01943.hp2 HG02135.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.84+154_84+155insAC others(160): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
GCCGCGCG others(11): Show |
G | 1 | a0001c0001t0002g0297 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.84+137_84+154delAC others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712349
|
GCCGCGCG others(29): Show |
G | 1 | a0002c0002t0002g0319 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.84+119_84+154delAC others(34): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712349 | ||||||
chr18:712356
|
G | GTACCATG others(11): Show |
27 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0250others(24): Show | 28 | HG00673.hp2 HG00741.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.84+130_84+147dupAG others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712356
|
G | GTACCATG others(29): Show |
12 | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0220others(9): Show | 12 | HG00558.hp2 HG00738.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.84+112_84+147dupAG others(34): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712356
|
G | GTACCATG others(47): Show |
3 | a0001c0001t0001g0188a0001c0001t0001g0189a0005c0009t0001g0190 | 3 | NA18960.hp2 NA19083.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.84+94_84+147dupAGC others(51): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712356
|
G | GTACCATG others(65): Show |
1 | a0002c0002t0011g0151 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.84+76_84+147dupAGC others(69): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712356
|
G | T | 266 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0084others(263): Show | 277 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.84+148C>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712356
|
GTACCATG others(11): Show |
G | 23 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0305others(20): Show | 25 | HG00639.hp1 HG01069.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.84+130_84+147delAG others(16): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712356
|
GTACCATG others(29): Show |
G | 20 | a0001c0001t0001g0010a0001c0001t0001g0322a0001c0001t0001g0323others(17): Show | 21 | HG00280.hp2 HG00597.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.84+112_84+147delAG others(34): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712356
|
GTACCATG others(47): Show |
G | 4 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0003t0001g0340others(1): Show | 4 | HG00735.hp1 HG02976.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.84+94_84+147delAGC others(51): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712356
|
GTACCATG others(65): Show |
G | 2 | a0001c0001t0001g0342a0001c0003t0001g0341 | 2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.84+76_84+147delAGC others(69): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712356 | ||||||
chr18:712365
|
C | T | 1 | a0001c0001t0002g0015 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.84+139G>A | ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712365 | ||||||
chr18:712476
|
CCGCGCTT others(10): Show |
C | 1 | a0001c0001t0001g0343 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.84+11_84+27delACGC others(13): Show |
ENOSF1 | ENSG00000132199.20 | transcript | ENST00000647584.2 | protein_coding | 1/15 | chr18 | 712476 |