geneid | 23149 |
---|---|
ensemblid | ENSG00000130475.16 |
hgncid | 29002 |
symbol | FCHO1 |
name | FCH and mu domain containing endocytic adaptor 1 |
refseq_nuc | NM_015122.3 |
refseq_prot | NP_055937.1 |
ensembl_nuc | ENST00000596536.6 |
ensembl_prot | ENSP00000470731.1 |
mane_status | MANE Select |
chr | chr19 |
start | 17751477 |
end | 17788561 |
strand | + |
ver | v1.2 |
region | chr19:17751477-17788561 |
region5000 | chr19:17746477-17793561 |
regionname0 | FCHO1_chr19_17751477_17788561 |
regionname5000 | FCHO1_chr19_17746477_17793561 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 889 | 343 | 90 | 78 | 113 | 14 | 46 | 74 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0002 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0003 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0004 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0005 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0006 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0007 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0008 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0009 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0010 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2670 | 187 | 48 | 35 | 77 | 5 | 22 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0002 | 1/0 | 2670 | 57 | 21 | 8 | 20 | 0 | 7 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0003 | 0/1 | 2670 | 38 | 5 | 12 | 3 | 6 | 11 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0004 | 0/0 | 2670 | 34 | 7 | 14 | 4 | 3 | 6 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0005 | 0/0 | 2670 | 13 | 0 | 6 | 7 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0006 | 0/0 | 2670 | 5 | 5 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0007 | 0/0 | 2670 | 3 | 2 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0008 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0009 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0010 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0011 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0012 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0013 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0014 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0015 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0016 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0017 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0018 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0019 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0020 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0021 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
c0022 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 539 | 290 | 78 | 58 | 109 | 9 | 34 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0002 | 0/0 | 539 | 35 | 9 | 14 | 3 | 3 | 6 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0003 | 0/0 | 539 | 10 | 5 | 1 | 2 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0004 | 0/0 | 539 | 4 | 0 | 2 | 0 | 2 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0005 | 0/0 | 539 | 3 | 0 | 1 | 0 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0006 | 0/0 | 539 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0007 | 0/0 | 539 | 2 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0008 | 0/0 | 539 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0009 | 0/0 | 539 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0010 | 0/0 | 539 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0011 | 0/0 | 539 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0012 | 0/0 | 539 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
t0013 | 0/0 | 524 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0308 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2670 | 187 | 48 | 35 | 77 | 5 | 22 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0002 | 1/0 | 2670 | 57 | 21 | 8 | 20 | 0 | 7 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0003 | 0/1 | 2670 | 38 | 5 | 12 | 3 | 6 | 11 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0004 | 0/0 | 2670 | 34 | 7 | 14 | 4 | 3 | 6 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0005 | 0/0 | 2670 | 13 | 0 | 6 | 7 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0006 | 0/0 | 2670 | 5 | 5 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0007 | 0/0 | 2670 | 3 | 2 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0008 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0009 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0011 | 0/0 | 2670 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0012 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0016 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0017 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0002c0022 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0003c0021 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0004c0019 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0005c0018 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0006c0013 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0007c0014 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0008c0015 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0009c0020 | 0/0 | 2670 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0010c0010 | 0/0 | 2670 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3208 | 182 | 48 | 34 | 76 | 5 | 19 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0001t0002 | 0/0 | 3208 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0001t0005 | 0/0 | 3208 | 3 | 0 | 1 | 0 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0001t0009 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0002t0001 | 1/0 | 3208 | 48 | 16 | 8 | 17 | 0 | 6 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0002t0002 | 0/0 | 3208 | 4 | 3 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0002t0006 | 0/0 | 3208 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0002t0008 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0002t0012 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0002t0013 | 0/0 | 3193 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0003t0001 | 0/1 | 3208 | 29 | 5 | 9 | 1 | 4 | 9 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0003t0002 | 0/0 | 3208 | 3 | 0 | 0 | 2 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0003t0004 | 0/0 | 3208 | 4 | 0 | 2 | 0 | 2 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0003t0007 | 0/0 | 3208 | 2 | 0 | 1 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0004t0001 | 0/0 | 3208 | 2 | 0 | 1 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0004t0002 | 0/0 | 3208 | 22 | 3 | 12 | 1 | 3 | 3 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0004t0003 | 0/0 | 3208 | 8 | 4 | 0 | 2 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0004t0010 | 0/0 | 3208 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0004t0011 | 0/0 | 3208 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0005t0001 | 0/0 | 3208 | 13 | 0 | 6 | 7 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0006t0001 | 0/0 | 3208 | 5 | 5 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0007t0002 | 0/0 | 3208 | 2 | 1 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0007t0003 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0008t0003 | 0/0 | 3208 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0009t0002 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0011t0002 | 0/0 | 3208 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0012t0001 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0016t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0001c0017t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0002c0022t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0003c0021t0001 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0004c0019t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0005c0018t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0006c0013t0001 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0007c0014t0001 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0008c0015t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0009c0020t0001 | 0/0 | 3208 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
a0010c0010t0002 | 0/0 | 3208 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | copy fasta | chr19 | 17746477 | 17793561 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0005g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0005g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0001t0009g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0002t0013g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0308 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0004g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0007g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0003t0007g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0010g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0004t0011g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0001 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0005t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0006t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0007t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0007t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0007t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0008t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0009t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0011t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0012t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0016t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0001c0017t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0002c0022t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0003c0021t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0004c0019t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0005c0018t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0006c0013t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0007c0014t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0008c0015t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0009c0020t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
a0010c0010t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0277 | EUR | GBR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00140 | hp1 | a0001 | c0004 | t0002 | g0034 | EUR | GBR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0274 | EUR | GBR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | FIN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00280 | hp2 | a0001 | c0004 | t0002 | g0038 | EUR | FIN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | FIN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0016 | EUR | FIN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00639 | hp2 | a0001 | c0005 | t0001 | g0133 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00673 | hp2 | a0005 | c0018 | t0001 | g0298 | EAS | CHS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00733 | hp2 | a0001 | c0008 | t0003 | g0020 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00738 | hp2 | a0001 | c0004 | t0002 | g0002 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0316 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01069 | hp2 | a0001 | c0005 | t0001 | g0114 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01070 | hp1 | a0001 | c0004 | t0002 | g0042 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01071 | hp1 | a0001 | c0004 | t0002 | g0002 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0236 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01099 | hp2 | a0001 | c0003 | t0004 | g0155 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0156 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01175 | hp2 | a0001 | c0003 | t0004 | g0160 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0195 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01255 | hp1 | a0001 | c0004 | t0002 | g0035 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01256 | hp1 | a0001 | c0003 | t0001 | g0158 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0257 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01257 | hp1 | a0001 | c0005 | t0001 | g0105 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01257 | hp2 | a0001 | c0004 | t0002 | g0015 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0157 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01258 | hp2 | a0001 | c0004 | t0002 | g0014 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01346 | hp1 | a0001 | c0004 | t0002 | g0037 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01358 | hp1 | a0001 | c0011 | t0002 | g0060 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01433 | hp2 | a0001 | c0004 | t0002 | g0039 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | IBS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01516 | hp2 | a0001 | c0003 | t0004 | g0146 | EUR | IBS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01517 | hp1 | a0001 | c0003 | t0004 | g0145 | EUR | IBS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01517 | hp2 | a0001 | c0003 | t0001 | g0154 | EUR | IBS | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01884 | hp2 | a0001 | c0004 | t0003 | g0017 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01934 | hp1 | a0001 | c0004 | t0001 | g0175 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01943 | hp2 | a0001 | c0005 | t0001 | g0132 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01975 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01993 | hp1 | a0001 | c0004 | t0010 | g0036 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02004 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02004 | hp2 | a0001 | c0004 | t0002 | g0028 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02055 | hp2 | a0001 | c0002 | t0006 | g0182 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02145 | hp2 | a0007 | c0014 | t0001 | g0049 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02148 | hp2 | a0001 | c0004 | t0002 | g0026 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | CDX | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0108 | EAS | CDX | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CDX | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02258 | hp1 | a0001 | c0002 | t0006 | g0188 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02258 | hp2 | a0001 | c0007 | t0003 | g0331 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02273 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0242 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02280 | hp1 | a0001 | c0004 | t0002 | g0023 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02293 | hp2 | a0001 | c0004 | t0002 | g0012 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02300 | hp2 | a0001 | c0003 | t0007 | g0147 | AMR | PEL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0098 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02523 | hp1 | a0001 | c0001 | t0009 | g0213 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02572 | hp1 | a0001 | c0004 | t0003 | g0022 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02602 | hp1 | a0001 | c0004 | t0002 | g0040 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02630 | hp2 | a0001 | c0006 | t0001 | g0179 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0162 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02698 | hp2 | a0001 | c0004 | t0002 | g0029 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0254 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0204 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02818 | hp2 | a0010 | c0010 | t0002 | g0140 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02895 | hp2 | a0001 | c0006 | t0001 | g0168 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02965 | hp1 | a0001 | c0012 | t0001 | g0142 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0064 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02976 | hp1 | a0001 | c0004 | t0003 | g0024 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0165 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03041 | hp2 | a0001 | c0006 | t0001 | g0169 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0138 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03139 | hp1 | a0001 | c0007 | t0002 | g0139 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03209 | hp1 | a0001 | c0004 | t0003 | g0018 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03209 | hp2 | a0001 | c0009 | t0002 | g0333 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03239 | hp1 | a0001 | c0004 | t0011 | g0003 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03239 | hp2 | a0001 | c0004 | t0002 | g0032 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03453 | hp2 | a0001 | c0006 | t0001 | g0171 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0149 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03491 | hp1 | a0001 | c0003 | t0007 | g0161 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03516 | hp1 | a0006 | c0013 | t0001 | g0225 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ESN | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0342 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03704 | hp2 | a0001 | c0004 | t0003 | g0019 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0173 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03710 | hp2 | a0001 | c0004 | t0003 | g0031 | SAS | PJL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0205 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0263 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0006 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0143 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0152 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0163 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0148 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG04228 | hp2 | a0001 | c0003 | t0002 | g0044 | SAS | STU | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18612 | hp1 | a0001 | c0017 | t0001 | g0267 | EAS | CHB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0166 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18957 | hp2 | a0001 | c0002 | t0008 | g0122 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18962 | hp2 | a0001 | c0016 | t0001 | g0232 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18966 | hp2 | a0001 | c0005 | t0001 | g0112 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18970 | hp2 | a0001 | c0005 | t0001 | g0106 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18971 | hp1 | a0001 | c0005 | t0001 | g0001 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18971 | hp2 | a0009 | c0020 | t0001 | g0198 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18977 | hp1 | a0001 | c0005 | t0001 | g0118 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18979 | hp1 | a0008 | c0015 | t0001 | g0336 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18980 | hp2 | a0001 | c0004 | t0003 | g0033 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18985 | hp1 | a0004 | c0019 | t0001 | g0324 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18989 | hp1 | a0002 | c0022 | t0001 | g0131 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18990 | hp2 | a0001 | c0005 | t0001 | g0117 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18991 | hp1 | a0001 | c0003 | t0002 | g0045 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18994 | hp1 | a0001 | c0003 | t0002 | g0043 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19010 | hp2 | a0001 | c0005 | t0001 | g0115 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19011 | hp1 | a0001 | c0002 | t0013 | g0083 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19030 | hp1 | a0001 | c0004 | t0002 | g0027 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19056 | hp2 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19070 | hp1 | a0001 | c0005 | t0001 | g0113 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19080 | hp2 | a0001 | c0002 | t0012 | g0129 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19087 | hp2 | a0001 | c0004 | t0003 | g0030 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0085 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ASW | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | ASW | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20752 | hp1 | a0001 | c0004 | t0002 | g0208 | EUR | TSI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0159 | EUR | TSI | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | GIH | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | GIH | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0216 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG01123 | hp2 | a0001 | c0007 | t0002 | g0332 | AMR | CLM | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0063 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02109 | hp2 | a0003 | c0021 | t0001 | g0135 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG02559 | hp2 | a0001 | c0004 | t0002 | g0041 | AFR | ACB | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0091 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | USA | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | USA | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0170 | AFR | USA | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | USA | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0101 | AFR | LWK | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0308 | REF | REF | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0102 | REF | REF | FCHO1_chr19_17746477_17793561 | FCHO1 | chr19 | 17746477 | 17793561 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17754311
|
TTGCAGAT others(13): Show |
T | 1 | a0001 | 1 | NA19011.hp1 | splice_acceptor_variant&splice_region_variant&5_prime_UTR_variant&intron_variant | HIGH | c.-182-5_-168delTGCA others(16): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/29 | 834 | chr19 | 17754311 | |||||
chr19:17764410
|
C | T | 1 | a0010 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.155C>T | p.Ala52Val | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/29 | 438/3208 | 155/2670 | 52/889 | chr19 | 17764410 | ||
chr19:17766690
|
G | T | 1 | a0002 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.216G>T | p.Glu72Asp | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/29 | 499/3208 | 216/2670 | 72/889 | chr19 | 17766690 | ||
chr19:17770831
|
C | T | 1 | a0003 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.529C>T | p.Arg177Cys | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/29 | 812/3208 | 529/2670 | 177/889 | chr19 | 17770831 | ||
chr19:17774415
|
C | T | 1 | a0009 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.857C>T | p.Ala286Val | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1140/3208 | 857/2670 | 286/889 | chr19 | 17774415 | ||
chr19:17774444
|
C | G | 1 | a0004 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.886C>G | p.Arg296Gly | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1169/3208 | 886/2670 | 296/889 | chr19 | 17774444 | ||
chr19:17774447
|
C | G | 1 | a0004 | 1 | NA18985.hp1 | missense_variant | MODERATE | c.889C>G | p.Arg297Gly | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1172/3208 | 889/2670 | 297/889 | chr19 | 17774447 | ||
chr19:17775486
|
A | T | 1 | a0005 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.976A>T | p.Thr326Ser | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/29 | 1259/3208 | 976/2670 | 326/889 | chr19 | 17775486 | ||
chr19:17784795
|
C | A | 1 | a0006 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2297C>A | p.Thr766Asn | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/29 | 2580/3208 | 2297/2670 | 766/889 | chr19 | 17784795 | ||
chr19:17784899
|
G | A | 1 | a0007 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.2401G>A | p.Val801Ile | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/29 | 2684/3208 | 2401/2670 | 801/889 | chr19 | 17784899 | ||
chr19:17787783
|
G | A | 1 | a0008 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.2584G>A | p.Val862Met | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/29 | 2867/3208 | 2584/2670 | 862/889 | chr19 | 17787783 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17755170
|
G | A | 1 | a0001c0008 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.6G>A | p.Ser2Ser | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/29 | 289/3208 | 6/2670 | 2/889 | chr19 | 17755170 | ||
chr19:17755179
|
G | C | 3 | a0001c0007a0001c0009a0010c0010 | 5 | HG01123.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.15G>C | p.Gly5Gly | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/29 | 298/3208 | 15/2670 | 5/889 | chr19 | 17755179 | ||
chr19:17766765
|
G | A | 1 | a0001c0011 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.291G>A | p.Lys97Lys | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/29 | 574/3208 | 291/2670 | 97/889 | chr19 | 17766765 | ||
chr19:17774446
|
G | C | 1 | a0004c0019 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.888G>C | p.Arg296Arg | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1171/3208 | 888/2670 | 296/889 | chr19 | 17774446 | ||
chr19:17774461
|
A | G | 13 | a0001c0001a0001c0005a0001c0006others(10): Show | 215 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(212): Show |
synonymous_variant | LOW | c.903A>G | p.Pro301Pro | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/29 | 1186/3208 | 903/2670 | 301/889 | chr19 | 17774461 | ||
chr19:17775071
|
C | T | 2 | a0001c0004a0001c0008 | 35 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(32): Show |
synonymous_variant | LOW | c.936C>T | p.Pro312Pro | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 14/29 | 1219/3208 | 936/2670 | 312/889 | chr19 | 17775071 | ||
chr19:17776131
|
G | A | 12 | a0001c0001a0001c0006a0001c0009others(9): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
synonymous_variant | LOW | c.1152G>A | p.Ala384Ala | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 16/29 | 1435/3208 | 1152/2670 | 384/889 | chr19 | 17776131 | ||
chr19:17781283
|
A | G | 1 | a0001c0017 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.1680A>G | p.Pro560Pro | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 21/29 | 1963/3208 | 1680/2670 | 560/889 | chr19 | 17781283 | ||
chr19:17781782
|
A | G | 16 | a0001c0001a0001c0003a0001c0004others(13): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
synonymous_variant | LOW | c.1899A>G | p.Thr633Thr | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/29 | 2182/3208 | 1899/2670 | 633/889 | chr19 | 17781782 | ||
chr19:17781794
|
C | T | 2 | a0001c0012a0001c0016 | 2 | HG02965.hp1 NA18962.hp2 |
synonymous_variant | LOW | c.1911C>T | p.His637His | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/29 | 2194/3208 | 1911/2670 | 637/889 | chr19 | 17781794 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17751531
|
G | A | 1 | a0001c0002t0008 | 1 | NA18957.hp2 | 5_prime_UTR_variant | MODIFIER | c.-229G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/29 | 3634 | chr19 | 17751531 | |||||
chr19:17754340
|
T | G | 1 | a0001c0001t0009 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/29 | 825 | chr19 | 17754340 | |||||
chr19:17754341
|
G | A | 1 | a0001c0004t0010 | 1 | HG01993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-158G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/29 | 824 | chr19 | 17754341 | |||||
chr19:17754667
|
A | G | 2 | a0001c0003t0004a0001c0003t0007 | 6 | HG01099.hp2 HG01175.hp2 HG01516.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-62A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/29 | chr19 | 17754667 | ||||||
chr19:17754670
|
T | G | 13 | a0001c0001t0002a0001c0002t0002a0001c0003t0002others(10): Show | 47 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-59T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/29 | 495 | chr19 | 17754670 | |||||
chr19:17755155
|
G | A | 1 | a0001c0002t0012 | 1 | NA19080.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/29 | 10 | chr19 | 17755155 | |||||
chr19:17788324
|
C | T | 1 | a0001c0002t0006 | 2 | HG02055.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*18C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 29/29 | 18 | chr19 | 17788324 | |||||
chr19:17788457
|
C | G | 1 | a0001c0004t0011 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 29/29 | 151 | chr19 | 17788457 | |||||
chr19:17788458
|
C | T | 5 | a0001c0001t0005a0001c0003t0007a0001c0004t0003others(2): Show | 15 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*152C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 29/29 | 152 | chr19 | 17788458 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:17751608
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-183+31A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17751608 | ||||||
chr19:17751727
|
C | T | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-183+150C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17751727 | ||||||
chr19:17751819
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-183+242C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17751819 | ||||||
chr19:17752116
|
C | G | 166 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0177others(163): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.-183+539C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752116 | ||||||
chr19:17752149
|
A | G | 1 | a0001c0001t0001g0338 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-183+572A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752149 | ||||||
chr19:17752158
|
C | T | 1 | a0001c0002t0001g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-183+581C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752158 | ||||||
chr19:17752226
|
T | TTGTA | 16 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0050others(13): Show | 16 | HG01167.hp1 HG01169.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.-183+679_-183+682d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752226 | |||||
chr19:17752226
|
T | TTGTATGT others(1): Show |
40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(37): Show | 41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.-183+675_-183+682d others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752226 | |||||
chr19:17752226
|
TTGTA | T | 198 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0151others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.-183+679_-183+682d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752226 | |||||
chr19:17752226
|
TTGTATGT others(5): Show |
T | 2 | a0001c0001t0001g0337a0001c0001t0001g0339 | 2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-183+671_-183+682d others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752226 | |||||
chr19:17752304
|
G | T | 258 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(255): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-183+727G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752304 | ||||||
chr19:17752345
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-183+768G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752345 | ||||||
chr19:17752345
|
G | T | 2 | a0001c0002t0002g0061a0001c0011t0002g0060 | 2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-183+768G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752345 | ||||||
chr19:17752361
|
T | C | 271 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(268): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-183+784T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752361 | ||||||
chr19:17752416
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-183+839G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752416 | ||||||
chr19:17752485
|
C | T | 4 | a0001c0002t0001g0134a0001c0002t0001g0136a0001c0002t0001g0137others(1): Show | 4 | HG02055.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-183+908C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752485 | ||||||
chr19:17752508
|
CCTCGGCC others(17): Show |
C | 155 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0177others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.-183+932_-183+955d others(26): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752508 | ||||||
chr19:17752512
|
G | A | 110 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0025others(107): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.-183+935G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752512 | ||||||
chr19:17752534
|
A | T | 155 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0177others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.-183+957A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752534 | ||||||
chr19:17752535
|
C | G | 155 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0177others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.-183+958C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752535 | ||||||
chr19:17752736
|
C | CA | 175 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0048others(172): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-183+1176dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752736 | |||||
chr19:17752736
|
C | CAA | 9 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0001g0194others(6): Show | 9 | HG01192.hp2 HG02132.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.-183+1175_-183+117 others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | 17752736 | |||||
chr19:17752754
|
T | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0051others(9): Show | 12 | HG01167.hp1 HG01169.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-183+1177T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752754 | ||||||
chr19:17752833
|
G | A | 2 | a0001c0004t0002g0014a0001c0004t0002g0015 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-183+1256G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752833 | ||||||
chr19:17752842
|
A | G | 2 | a0001c0002t0002g0061a0001c0011t0002g0060 | 2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-183+1265A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752842 | ||||||
chr19:17752919
|
T | A | 1 | a0009c0020t0001g0198 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-183+1342T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17752919 | ||||||
chr19:17753037
|
G | A | 3 | a0001c0002t0001g0078a0001c0002t0001g0079a0001c0002t0001g0080 | 3 | HG02895.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-182-1280G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753037 | ||||||
chr19:17753069
|
G | A | 10 | a0001c0001t0001g0025a0001c0001t0002g0021a0001c0003t0001g0016others(7): Show | 10 | HG00323.hp2 HG00733.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-182-1248G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753069 | ||||||
chr19:17753184
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-182-1133A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753184 | ||||||
chr19:17753235
|
G | T | 1 | a0001c0001t0001g0330 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-182-1082G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753235 | ||||||
chr19:17753236
|
T | C | 257 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-182-1081T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753236 | ||||||
chr19:17753303
|
A | C | 4 | a0001c0002t0002g0046a0001c0003t0002g0043a0001c0003t0002g0044others(1): Show | 4 | HG03688.hp2 HG04228.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.-182-1014A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753303 | ||||||
chr19:17753394
|
C | T | 38 | a0001c0001t0001g0025a0001c0001t0002g0021a0001c0002t0002g0046others(35): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.-182-923C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753394 | ||||||
chr19:17753545
|
A | G | 253 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(250): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-182-772A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753545 | ||||||
chr19:17753643
|
T | C | 257 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0025others(254): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-182-674T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753643 | ||||||
chr19:17753705
|
C | T | 2 | a0001c0001t0001g0328a0001c0001t0001g0329 | 2 | NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-182-612C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753705 | ||||||
chr19:17753891
|
T | C | 256 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(253): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.-182-426T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17753891 | ||||||
chr19:17754009
|
G | T | 1 | a0001c0001t0001g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-182-308G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17754009 | ||||||
chr19:17754111
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-182-206C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 1/28 | chr19 | 17754111 | ||||||
chr19:17754400
|
G | T | 1 | a0001c0005t0001g0133 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-138+39G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/28 | chr19 | 17754400 | ||||||
chr19:17754433
|
G | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-138+72G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/28 | chr19 | 17754433 | ||||||
chr19:17754496
|
T | C | 259 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(256): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-137-96T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 2/28 | chr19 | 17754496 | ||||||
chr19:17754759
|
G | T | 3 | a0001c0001t0001g0326a0001c0001t0001g0327a0008c0015t0001g0336 | 3 | HG02523.hp2 NA18979.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-48+78G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/28 | chr19 | 17754759 | ||||||
chr19:17754768
|
C | T | 1 | a0001c0001t0001g0325 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-48+87C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/28 | chr19 | 17754768 | ||||||
chr19:17754964
|
G | T | 1 | a0001c0012t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-47-154G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/28 | chr19 | 17754964 | ||||||
chr19:17755032
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-47-86T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 3/28 | chr19 | 17755032 | ||||||
chr19:17755266
|
T | A | 1 | a0007c0014t0001g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.27+75T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755266 | ||||||
chr19:17755379
|
C | A | 1 | a0001c0001t0001g0008 | 2 | HG00733.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.27+188C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755379 | ||||||
chr19:17755391
|
A | G | 1 | a0001c0002t0001g0138 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.27+200A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755391 | ||||||
chr19:17755538
|
C | T | 255 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(252): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.27+347C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755538 | ||||||
chr19:17755675
|
T | TA | 34 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(31): Show | 36 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.27+485dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17755675 | |||||
chr19:17755936
|
T | C | 242 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(239): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.27+745T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17755936 | ||||||
chr19:17756024
|
A | G | 2 | a0001c0002t0001g0138a0001c0012t0001g0142 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.27+833A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756024 | ||||||
chr19:17756144
|
T | A | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.27+953T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756144 | ||||||
chr19:17756244
|
C | T | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.27+1053C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756244 | ||||||
chr19:17756370
|
G | A | 3 | a0001c0003t0004g0145a0001c0003t0004g0146a0001c0003t0007g0147 | 3 | HG01516.hp2 HG01517.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.27+1179G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756370 | ||||||
chr19:17756646
|
C | T | 1 | a0001c0002t0002g0046 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+1455C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756646 | ||||||
chr19:17756733
|
G | A | 4 | a0001c0002t0002g0046a0001c0003t0002g0043a0001c0003t0002g0044others(1): Show | 4 | HG03688.hp2 HG04228.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.27+1542G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756733 | ||||||
chr19:17756737
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG01928.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.27+1546T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756737 | ||||||
chr19:17756765
|
C | G | 1 | a0001c0001t0001g0323 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.27+1574C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756765 | ||||||
chr19:17756796
|
A | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.27+1605A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756796 | ||||||
chr19:17756803
|
T | C | 31 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(28): Show | 33 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.27+1612T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756803 | ||||||
chr19:17756821
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.27+1630G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756821 | ||||||
chr19:17756915
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 7 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+1724G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17756915 | ||||||
chr19:17757087
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.27+1896G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757087 | ||||||
chr19:17757114
|
G | A | 89 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047others(86): Show | 92 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.27+1923G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757114 | ||||||
chr19:17757165
|
T | C | 1 | a0001c0002t0001g0078 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.27+1974T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757165 | ||||||
chr19:17757170
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.27+1979T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757170 | ||||||
chr19:17757177
|
C | A | 2 | a0001c0003t0004g0145a0001c0003t0004g0146 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.27+1986C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757177 | ||||||
chr19:17757182
|
T | TA | 32 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0050others(29): Show | 32 | HG00639.hp1 HG00735.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.27+2013dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757182 | |||||
chr19:17757182
|
TA | T | 9 | a0001c0001t0001g0322a0001c0004t0002g0042a0001c0005t0001g0132others(6): Show | 9 | HG01070.hp1 HG01943.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+2013delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757182 | |||||
chr19:17757303
|
A | G | 50 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047others(47): Show | 51 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.27+2112A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757303 | ||||||
chr19:17757401
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.27+2210G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757401 | ||||||
chr19:17757401
|
G | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2210G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757401 | ||||||
chr19:17757405
|
G | A | 2 | a0001c0001t0001g0328a0001c0001t0001g0329 | 2 | NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.27+2214G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757405 | ||||||
chr19:17757457
|
C | T | 2 | a0001c0002t0001g0138a0001c0012t0001g0142 | 2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.27+2266C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757457 | ||||||
chr19:17757477
|
G | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2286G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757477 | ||||||
chr19:17757485
|
G | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2294G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757485 | ||||||
chr19:17757505
|
T | A | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2314T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757505 | ||||||
chr19:17757512
|
A | G | 1 | a0001c0001t0001g0341 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.27+2321A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757512 | ||||||
chr19:17757520
|
G | A | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2329G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757520 | ||||||
chr19:17757550
|
A | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2359A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757550 | ||||||
chr19:17757557
|
A | AAGGTGGA others(4): Show |
1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2366_27+2367ins others(11): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757557 | ||||||
chr19:17757558
|
G | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2367G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757558 | ||||||
chr19:17757562
|
C | A | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2371C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757562 | ||||||
chr19:17757564
|
C | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2373C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757564 | ||||||
chr19:17757567
|
T | A | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2376T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757567 | ||||||
chr19:17757569
|
C | A | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2378C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757569 | ||||||
chr19:17757570
|
G | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2379G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757570 | ||||||
chr19:17757579
|
G | A | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2388G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757579 | ||||||
chr19:17757602
|
A | G | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2411A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757602 | ||||||
chr19:17757610
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.27+2419C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757610 | ||||||
chr19:17757612
|
A | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2421A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757612 | ||||||
chr19:17757633
|
A | G | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2442A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757633 | ||||||
chr19:17757634
|
G | A | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2443G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757634 | ||||||
chr19:17757653
|
C | T | 3 | a0001c0003t0001g0164a0001c0003t0001g0165a0001c0003t0001g0166 | 3 | HG02886.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.27+2462C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757653 | ||||||
chr19:17757658
|
G | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2467G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757658 | ||||||
chr19:17757660
|
A | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2469A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757660 | ||||||
chr19:17757663
|
C | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2472C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757663 | ||||||
chr19:17757664
|
C | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2473C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757664 | ||||||
chr19:17757665
|
A | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2474A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757665 | ||||||
chr19:17757666
|
A | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2475A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757666 | ||||||
chr19:17757667
|
A | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2476A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757667 | ||||||
chr19:17757674
|
G | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2483G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757674 | ||||||
chr19:17757675
|
A | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2484A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757675 | ||||||
chr19:17757676
|
G | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2485G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757676 | ||||||
chr19:17757677
|
A | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2486A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757677 | ||||||
chr19:17757678
|
A | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2487A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757678 | ||||||
chr19:17757679
|
G | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2488G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757679 | ||||||
chr19:17757682
|
G | A | 5 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2491G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757682 | ||||||
chr19:17757682
|
G | C | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2491G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757682 | ||||||
chr19:17757683
|
A | T | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2492A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757683 | ||||||
chr19:17757694
|
C | T | 5 | a0001c0001t0001g0167a0001c0002t0002g0061a0001c0002t0002g0063others(2): Show | 5 | HG01358.hp1 HG02109.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2503C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757694 | ||||||
chr19:17757894
|
C | T | 1 | a0001c0001t0001g0320 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.27+2703C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757894 | ||||||
chr19:17757915
|
C | A | 1 | a0001c0002t0013g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.27+2724C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757915 | ||||||
chr19:17757915
|
C | CA | 30 | a0001c0001t0001g0050a0001c0001t0001g0084a0001c0001t0001g0178others(27): Show | 30 | HG01123.hp1 HG01261.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.27+2744dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757915 | |||||
chr19:17757915
|
CA | C | 9 | a0001c0001t0001g0180a0001c0001t0001g0199a0001c0001t0001g0200others(6): Show | 9 | HG01243.hp1 HG01516.hp1 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.27+2744delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757915 | |||||
chr19:17757915
|
CAA | C | 32 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0138others(29): Show | 34 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.27+2743_27+2744del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17757915 | |||||
chr19:17757982
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.27+2791G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17757982 | ||||||
chr19:17758102
|
C | T | 5 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+2911C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758102 | ||||||
chr19:17758132
|
G | A | 1 | a0001c0012t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.27+2941G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758132 | ||||||
chr19:17758572
|
T | C | 1 | a0006c0013t0001g0225 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.27+3381T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758572 | ||||||
chr19:17758789
|
A | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0077 | 2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.27+3598A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758789 | ||||||
chr19:17758825
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 7 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+3634C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758825 | ||||||
chr19:17758835
|
C | A | 301 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.27+3644C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758835 | ||||||
chr19:17758925
|
G | T | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.27+3734G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758925 | ||||||
chr19:17758992
|
A | G | 2 | a0001c0001t0001g0317a0001c0001t0001g0318 | 2 | HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.28-3770A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17758992 | ||||||
chr19:17759009
|
G | A | 301 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(298): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.28-3753G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759009 | ||||||
chr19:17759036
|
G | T | 174 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.28-3726G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759036 | ||||||
chr19:17759084
|
G | A | 3 | a0001c0001t0001g0226a0001c0001t0001g0328a0001c0001t0001g0329 | 3 | HG03834.hp2 NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.28-3678G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759084 | ||||||
chr19:17759101
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.28-3661T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759101 | ||||||
chr19:17759136
|
A | T | 3 | a0001c0002t0002g0061a0001c0003t0001g0101a0001c0011t0002g0060 | 3 | HG01358.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-3626A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759136 | ||||||
chr19:17759200
|
A | G | 1 | a0001c0004t0002g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.28-3562A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759200 | ||||||
chr19:17759226
|
C | CT | 119 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(116): Show | 124 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.28-3522dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | |||||
chr19:17759226
|
C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0214a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG03490.hp1 NA18965.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.28-3533_28-3522dup others(12): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | |||||
chr19:17759226
|
C | CTTTTTTT others(6): Show |
149 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0071others(146): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.28-3534_28-3522dup others(13): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | |||||
chr19:17759226
|
C | CTTTTTTT others(7): Show |
63 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0070others(60): Show | 64 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.28-3535_28-3522dup others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | |||||
chr19:17759226
|
C | CTTTTTTT others(8): Show |
4 | a0001c0001t0001g0167a0001c0001t0001g0212a0001c0003t0001g0316others(1): Show | 4 | HG00741.hp1 HG01358.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-3522_28-3521ins others(15): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | |||||
chr19:17759226
|
C | CTTTTTTT others(9): Show |
1 | a0001c0003t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.28-3522_28-3521ins others(16): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759226 | |||||
chr19:17759655
|
G | A | 43 | a0001c0001t0001g0180a0001c0001t0002g0021a0001c0002t0001g0138others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.28-3107G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759655 | ||||||
chr19:17759752
|
G | C | 1 | a0001c0001t0001g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-3010G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759752 | ||||||
chr19:17759812
|
TA | T | 43 | a0001c0001t0001g0180a0001c0001t0002g0021a0001c0002t0001g0138others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.28-2940delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17759812 | |||||
chr19:17759908
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.28-2854A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17759908 | ||||||
chr19:17760009
|
C | T | 1 | a0001c0001t0001g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-2753C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760009 | ||||||
chr19:17760047
|
CT | C | 76 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0048others(73): Show | 79 | HG00423.hp2 HG00639.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.28-2700delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17760047 | |||||
chr19:17760047
|
CTT | C | 254 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(251): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.28-2701_28-2700del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17760047 | |||||
chr19:17760115
|
G | T | 24 | a0001c0001t0001g0062a0001c0001t0001g0196a0001c0001t0001g0197others(21): Show | 24 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.28-2647G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760115 | ||||||
chr19:17760302
|
C | T | 2 | a0001c0003t0001g0007a0001c0003t0001g0150 | 3 | HG01070.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.28-2460C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760302 | ||||||
chr19:17760332
|
T | G | 1 | a0001c0006t0001g0168 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.28-2430T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760332 | ||||||
chr19:17760423
|
G | A | 174 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(171): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.28-2339G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760423 | ||||||
chr19:17760547
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.28-2215A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760547 | ||||||
chr19:17760928
|
G | C | 222 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(219): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.28-1834G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760928 | ||||||
chr19:17760940
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.28-1822C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17760940 | ||||||
chr19:17761036
|
C | A | 1 | a0001c0002t0001g0202 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.28-1726C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761036 | ||||||
chr19:17761163
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.28-1599C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761163 | ||||||
chr19:17761260
|
C | T | 48 | a0001c0001t0001g0180a0001c0001t0002g0021a0001c0002t0001g0138others(45): Show | 49 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.28-1502C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761260 | ||||||
chr19:17761283
|
C | T | 48 | a0001c0001t0001g0180a0001c0001t0002g0021a0001c0002t0001g0138others(45): Show | 49 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.28-1479C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761283 | ||||||
chr19:17761401
|
C | CT | 252 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(249): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.28-1349dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761401 | |||||
chr19:17761438
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.28-1324T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761438 | ||||||
chr19:17761560
|
G | T | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.28-1202G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761560 | ||||||
chr19:17761633
|
C | CAT | 6 | a0001c0002t0001g0148a0001c0002t0001g0174a0001c0003t0001g0149others(3): Show | 6 | HG01496.hp1 HG01516.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-1109_28-1108dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATAT | 122 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0062others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.28-1111_28-1108dup others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATATAT | 28 | a0001c0001t0001g0081a0001c0001t0001g0181a0001c0001t0001g0183others(25): Show | 28 | HG00099.hp2 HG00741.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.28-1113_28-1108dup others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATATATA others(1): Show |
7 | a0001c0001t0001g0189a0001c0001t0001g0279a0001c0001t0001g0280others(4): Show | 7 | HG01891.hp2 HG02922.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-1115_28-1108dup others(8): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATATATA others(3): Show |
12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG02056.hp1 HG02071.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-1117_28-1108dup others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATATATA others(5): Show |
1 | a0001c0001t0005g0195 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.28-1119_28-1108dup others(12): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATATATA others(7): Show |
1 | a0001c0001t0001g0075 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.28-1121_28-1108dup others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATATATA others(9): Show |
1 | a0001c0001t0001g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.28-1123_28-1108dup others(16): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATATATA others(11): Show |
1 | a0001c0001t0001g0283 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.28-1125_28-1108dup others(18): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
C | CATATATA others(15): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01175.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.28-1108_28-1107ins others(22): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761633
|
CAT | C | 44 | a0001c0001t0001g0167a0001c0001t0001g0180a0001c0001t0002g0021others(41): Show | 45 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.28-1109_28-1108del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761633 | |||||
chr19:17761653
|
T | C | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0180 | 3 | HG02572.hp2 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.28-1109T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761653 | ||||||
chr19:17761653
|
T | TATATATA others(15): Show |
1 | a0001c0001t0001g0047 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.28-1108_28-1107ins others(22): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761653 | |||||
chr19:17761664
|
T | G | 1 | a0001c0001t0001g0339 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.28-1098T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761664 | ||||||
chr19:17761673
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.28-1089G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761673 | ||||||
chr19:17761729
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.28-1033C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761729 | ||||||
chr19:17761905
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.28-857C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761905 | ||||||
chr19:17761927
|
A | T | 1 | a0002c0022t0001g0131 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.28-835A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17761927 | ||||||
chr19:17761969
|
T | TTTCA | 163 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0053others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.28-766_28-763dupCA others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761969 | |||||
chr19:17761969
|
T | TTTCATTC others(1): Show |
54 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0071others(51): Show | 56 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.28-770_28-763dupCA others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761969 | |||||
chr19:17761969
|
T | TTTCATTC others(5): Show |
4 | a0001c0001t0001g0180a0001c0004t0002g0028a0001c0007t0002g0139others(1): Show | 4 | HG02004.hp2 HG02145.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-774_28-763dupCA others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761969 | |||||
chr19:17761969
|
T | TTTCATTC others(9): Show |
1 | a0001c0001t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-778_28-763dupCA others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17761969 | |||||
chr19:17762000
|
T | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 7 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-762T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762000 | ||||||
chr19:17762027
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.28-735C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762027 | ||||||
chr19:17762214
|
G | C | 2 | a0001c0002t0002g0061a0001c0011t0002g0060 | 2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.28-548G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762214 | ||||||
chr19:17762287
|
A | C | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.28-475A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762287 | ||||||
chr19:17762293
|
C | CT | 21 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0180others(18): Show | 22 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.28-455dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17762293 | |||||
chr19:17762293
|
C | CTT | 148 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0062others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.28-456_28-455dupTT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr19 | 17762293 | |||||
chr19:17762312
|
A | G | 5 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-450A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762312 | ||||||
chr19:17762530
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.28-232C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762530 | ||||||
chr19:17762606
|
A | G | 3 | a0001c0004t0001g0175a0001c0004t0002g0014a0001c0004t0002g0015 | 3 | HG01257.hp2 HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.28-156A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 4/28 | chr19 | 17762606 | ||||||
chr19:17762923
|
A | G | 1 | a0001c0001t0001g0322 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.119+70A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17762923 | ||||||
chr19:17763094
|
A | C | 341 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(338): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.119+241A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763094 | ||||||
chr19:17763196
|
A | C | 2 | a0001c0003t0001g0274a0001c0003t0001g0308 | 2 | HG00140.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.119+343A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763196 | ||||||
chr19:17763259
|
C | CT | 8 | a0001c0001t0001g0181a0001c0001t0001g0311a0001c0002t0001g0078others(5): Show | 8 | HG01361.hp1 HG01978.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.119+428dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763259 | |||||
chr19:17763259
|
CT | C | 204 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0062others(201): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.119+428delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763259 | |||||
chr19:17763259
|
CTT | C | 7 | a0001c0001t0001g0234a0001c0001t0001g0279a0001c0001t0001g0294others(4): Show | 7 | HG00558.hp2 HG02523.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.119+427_119+428del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763259 | |||||
chr19:17763501
|
C | T | 6 | a0001c0002t0001g0089a0001c0002t0001g0119a0001c0002t0001g0120others(3): Show | 6 | NA18945.hp2 NA18957.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.119+648C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763501 | ||||||
chr19:17763530
|
G | T | 1 | a0001c0003t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.119+677G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763530 | ||||||
chr19:17763553
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.119+700T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763553 | ||||||
chr19:17763563
|
C | CT | 120 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(117): Show | 123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.119+725dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763563 | |||||
chr19:17763563
|
C | CTT | 51 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0077others(48): Show | 51 | HG00099.hp1 HG00544.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.119+724_119+725dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763563 | |||||
chr19:17763563
|
C | CTTT | 12 | a0001c0001t0001g0192a0001c0001t0001g0221a0001c0001t0001g0269others(9): Show | 12 | HG00280.hp1 HG00423.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.119+723_119+725dup others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763563 | |||||
chr19:17763563
|
CT | C | 29 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(26): Show | 31 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.119+725delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17763563 | |||||
chr19:17763579
|
C | T | 225 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(222): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.119+726C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763579 | ||||||
chr19:17763650
|
C | T | 26 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(23): Show | 28 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.120-725C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763650 | ||||||
chr19:17763660
|
C | T | 3 | a0001c0001t0001g0167a0001c0002t0002g0061a0001c0011t0002g0060 | 3 | HG01358.hp1 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.120-715C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763660 | ||||||
chr19:17763735
|
A | T | 9 | a0001c0001t0001g0190a0001c0001t0001g0325a0001c0002t0002g0061others(6): Show | 9 | HG01358.hp1 HG01993.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.120-640A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763735 | ||||||
chr19:17763789
|
C | G | 5 | a0001c0001t0001g0197a0001c0001t0001g0223a0001c0001t0001g0312others(2): Show | 5 | HG00558.hp1 HG02056.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.120-586C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763789 | ||||||
chr19:17763927
|
C | T | 1 | a0001c0002t0001g0257 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.120-448C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17763927 | ||||||
chr19:17764044
|
C | CT | 170 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.120-318dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17764044 | |||||
chr19:17764044
|
C | CTT | 6 | a0001c0001t0001g0070a0001c0001t0001g0214a0001c0001t0001g0282others(3): Show | 6 | HG02071.hp2 HG02083.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.120-319_120-318dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr19 | 17764044 | |||||
chr19:17764165
|
C | T | 2 | a0001c0002t0002g0061a0001c0011t0002g0060 | 2 | HG01358.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.120-210C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17764165 | ||||||
chr19:17764214
|
T | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.120-161T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17764214 | ||||||
chr19:17764336
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0289 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.120-39C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17764336 | ||||||
chr19:17764350
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0230 | 2 | NA18941.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.120-25A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 5/28 | chr19 | 17764350 | ||||||
chr19:17764457
|
G | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0191 | 2 | HG01109.hp1 HG01891.hp2 |
splice_region_variant&intron_variant | LOW | c.194+8G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764457 | ||||||
chr19:17764465
|
G | T | 1 | a0001c0001t0001g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.194+16G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764465 | ||||||
chr19:17764508
|
T | A | 1 | a0001c0001t0001g0335 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.194+59T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764508 | ||||||
chr19:17764661
|
AGC | A | 43 | a0001c0001t0001g0180a0001c0001t0002g0021a0001c0002t0001g0138others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.194+213_194+214del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764661 | ||||||
chr19:17764755
|
T | A | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.194+306T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764755 | ||||||
chr19:17764814
|
C | G | 6 | a0001c0004t0002g0003a0001c0004t0002g0012a0001c0004t0002g0026others(3): Show | 6 | HG00280.hp2 HG01433.hp2 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.194+365C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764814 | ||||||
chr19:17764815
|
C | T | 1 | a0001c0002t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.194+366C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764815 | ||||||
chr19:17764871
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.194+422G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764871 | ||||||
chr19:17764896
|
C | G | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.194+447C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764896 | ||||||
chr19:17764933
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.194+484G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764933 | ||||||
chr19:17764946
|
C | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(172): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.194+497C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17764946 | ||||||
chr19:17765066
|
GA | G | 7 | a0001c0001t0001g0226a0001c0001t0001g0313a0001c0001t0001g0319others(4): Show | 7 | HG02523.hp1 HG03834.hp2 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.194+635delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765066 | |||||
chr19:17765213
|
G | A | 3 | a0001c0001t0001g0337a0001c0001t0001g0339a0007c0014t0001g0049 | 3 | HG02145.hp2 HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.194+764G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765213 | ||||||
chr19:17765235
|
G | GAAGGCCC others(8): Show |
1 | a0001c0001t0001g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.194+787_194+801dup others(15): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765235 | |||||
chr19:17765255
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.194+806C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765255 | ||||||
chr19:17765306
|
G | T | 1 | a0001c0003t0001g0101 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.194+857G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765306 | ||||||
chr19:17765384
|
C | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.194+935C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765384 | ||||||
chr19:17765530
|
G | A | 1 | a0001c0002t0001g0138 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.194+1081G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765530 | ||||||
chr19:17765533
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.194+1084C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765533 | ||||||
chr19:17765682
|
C | A | 1 | a0001c0001t0001g0295 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.195-987C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765682 | ||||||
chr19:17765756
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.195-913A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765756 | ||||||
chr19:17765856
|
T | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0312 | 2 | HG02056.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.195-813T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765856 | ||||||
chr19:17765882
|
C | CT | 35 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0047others(32): Show | 37 | HG01123.hp2 HG01175.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.195-763dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | |||||
chr19:17765882
|
C | CTT | 27 | a0001c0001t0001g0011a0001c0001t0002g0021a0001c0002t0001g0138others(24): Show | 28 | HG00280.hp2 HG00733.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.195-764_195-763dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | |||||
chr19:17765882
|
C | CTTT | 10 | a0001c0004t0002g0012a0001c0004t0002g0023a0001c0004t0002g0027others(7): Show | 10 | HG00140.hp1 HG01255.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.195-765_195-763dup others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | |||||
chr19:17765882
|
CT | C | 35 | a0001c0001t0001g0070a0001c0001t0001g0167a0001c0001t0001g0178others(32): Show | 35 | HG00280.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.195-763delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | |||||
chr19:17765882
|
CTT | C | 135 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(132): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.195-764_195-763del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17765882 | |||||
chr19:17765950
|
G | T | 16 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(13): Show | 16 | HG00544.hp2 HG01192.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.195-719G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17765950 | ||||||
chr19:17766090
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0116 | 2 | HG02135.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.195-579A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766090 | ||||||
chr19:17766177
|
A | AT | 17 | a0001c0001t0001g0011a0001c0001t0001g0059a0001c0001t0001g0070others(14): Show | 17 | HG01175.hp1 HG01175.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.195-475dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17766177 | |||||
chr19:17766177
|
AT | A | 6 | a0001c0001t0001g0279a0001c0002t0002g0061a0001c0004t0002g0013others(3): Show | 6 | HG01358.hp1 NA18522.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.195-475delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr19 | 17766177 | |||||
chr19:17766245
|
C | T | 2 | a0001c0001t0001g0266a0001c0001t0001g0338 | 2 | HG00423.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.195-424C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766245 | ||||||
chr19:17766270
|
G | A | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.195-399G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766270 | ||||||
chr19:17766348
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.195-321G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766348 | ||||||
chr19:17766414
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.195-255C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 6/28 | chr19 | 17766414 | ||||||
chr19:17766922
|
TCCGTTAA others(3): Show |
T | 1 | a0002c0022t0001g0131 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.336+114_336+123del others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17766922 | |||||
chr19:17767074
|
G | GT | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(264): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.336+276dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767074 | |||||
chr19:17767197
|
C | A | 41 | a0001c0001t0001g0180a0001c0003t0001g0141a0001c0004t0001g0175others(38): Show | 42 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.336+387C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767197 | ||||||
chr19:17767205
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.336+395A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767205 | ||||||
chr19:17767224
|
G | A | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0272 | 3 | HG00735.hp1 HG01168.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.336+414G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767224 | ||||||
chr19:17767333
|
A | C | 82 | a0001c0001t0001g0009a0001c0001t0001g0062a0001c0001t0001g0178others(79): Show | 83 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.336+523A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767333 | ||||||
chr19:17767385
|
C | T | 12 | a0001c0002t0013g0083a0001c0005t0001g0001a0001c0005t0001g0105others(9): Show | 14 | HG00639.hp2 HG01069.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.336+575C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767385 | ||||||
chr19:17767395
|
C | CAAAAAA | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(159): Show | 166 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.336+593_336+598dup others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767395 | |||||
chr19:17767395
|
C | CAAAAAAA | 23 | a0001c0001t0001g0048a0001c0001t0001g0066a0001c0001t0001g0072others(20): Show | 23 | HG00280.hp1 HG00544.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.336+592_336+598dup others(7): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767395 | |||||
chr19:17767395
|
CA | C | 83 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047others(80): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.336+598delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767395 | |||||
chr19:17767431
|
A | G | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(271): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.336+621A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767431 | ||||||
chr19:17767557
|
A | ACT | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+748_336+749dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767557 | |||||
chr19:17767563
|
T | TA | 76 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0001t0001g0180others(73): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.336+773dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767563 | |||||
chr19:17767563
|
T | TAA | 8 | a0001c0002t0002g0046a0001c0003t0001g0152a0001c0003t0001g0163others(5): Show | 8 | HG01175.hp2 HG03688.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.336+772_336+773dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767563 | |||||
chr19:17767563
|
T | TC | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(10): Show | 13 | HG00099.hp1 HG02132.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.336+753_336+754ins others(1): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767563 | ||||||
chr19:17767563
|
T | TCA | 143 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(140): Show | 146 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.336+753_336+754ins others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767563 | ||||||
chr19:17767563
|
T | TCAA | 26 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0048others(23): Show | 27 | HG01358.hp2 HG01891.hp1 HG01981.hp2 others(24): Show |
intron_variant | MODIFIER | c.336+753_336+754ins others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767563 | ||||||
chr19:17767563
|
T | TCAAA | 5 | a0001c0001t0001g0066a0001c0001t0001g0167a0001c0002t0002g0061others(2): Show | 5 | HG01358.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+753_336+754ins others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767563 | ||||||
chr19:17767563
|
TA | T | 8 | a0001c0002t0001g0080a0001c0002t0001g0086a0001c0002t0001g0098others(5): Show | 8 | HG01069.hp2 HG02451.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.336+773delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17767563 | |||||
chr19:17767574
|
A | C | 1 | a0001c0001t0001g0265 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.336+764A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767574 | ||||||
chr19:17767744
|
T | G | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.336+934T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767744 | ||||||
chr19:17767755
|
TG | T | 41 | a0001c0001t0001g0180a0001c0003t0001g0141a0001c0004t0001g0175others(38): Show | 42 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.336+946delG | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767755 | ||||||
chr19:17767870
|
T | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1060T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767870 | ||||||
chr19:17767913
|
A | G | 132 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0062others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.336+1103A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767913 | ||||||
chr19:17767966
|
T | C | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.336+1156T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17767966 | ||||||
chr19:17768024
|
T | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1214T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768024 | ||||||
chr19:17768042
|
G | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1232G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768042 | ||||||
chr19:17768082
|
T | C | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1272T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768082 | ||||||
chr19:17768126
|
G | A | 35 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(32): Show | 37 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.336+1316G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768126 | ||||||
chr19:17768157
|
C | A | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1347C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768157 | ||||||
chr19:17768213
|
T | C | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1403T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768213 | ||||||
chr19:17768295
|
C | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.336+1485C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768295 | ||||||
chr19:17768324
|
C | A | 1 | a0001c0003t0001g0316 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.336+1514C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768324 | ||||||
chr19:17768386
|
T | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.336+1576T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768386 | ||||||
chr19:17768411
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.336+1601G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768411 | ||||||
chr19:17768553
|
G | C | 19 | a0001c0001t0001g0004a0001c0001t0001g0025a0001c0001t0001g0048others(16): Show | 20 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.336+1743G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768553 | ||||||
chr19:17768584
|
C | T | 35 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(32): Show | 37 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.336+1774C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768584 | ||||||
chr19:17768589
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.336+1779G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768589 | ||||||
chr19:17768590
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.336+1780A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768590 | ||||||
chr19:17768618
|
T | C | 273 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(270): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.337-1807T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768618 | ||||||
chr19:17768618
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.337-1807T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768618 | ||||||
chr19:17768638
|
C | G | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1787C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768638 | ||||||
chr19:17768649
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.337-1776G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768649 | ||||||
chr19:17768709
|
C | CA | 57 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(54): Show | 60 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.337-1702dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17768709 | |||||
chr19:17768723
|
A | AAG | 6 | a0001c0001t0001g0190a0001c0001t0001g0220a0001c0001t0001g0238others(3): Show | 6 | HG02027.hp1 HG02083.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-1702_337-1701i others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768723 | ||||||
chr19:17768724
|
G | A | 31 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 32 | HG01175.hp1 HG01358.hp1 HG01496.hp2 others(29): Show |
intron_variant | MODIFIER | c.337-1701G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768724 | ||||||
chr19:17768724
|
G | GA | 159 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(156): Show | 162 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.337-1701_337-1700i others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768724 | ||||||
chr19:17768745
|
C | T | 25 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(22): Show | 26 | HG01175.hp1 HG01358.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.337-1680C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768745 | ||||||
chr19:17768760
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01175.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.337-1665T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768760 | ||||||
chr19:17768782
|
G | A | 5 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-1643G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768782 | ||||||
chr19:17768823
|
C | T | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1602C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17768823 | ||||||
chr19:17768984
|
T | TA | 187 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(184): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.337-1431dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17768984 | |||||
chr19:17769049
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.337-1376G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769049 | ||||||
chr19:17769086
|
G | T | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1339G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769086 | ||||||
chr19:17769148
|
G | C | 35 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(32): Show | 37 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.337-1277G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769148 | ||||||
chr19:17769227
|
A | G | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1198A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769227 | ||||||
chr19:17769241
|
C | T | 3 | a0001c0003t0001g0164a0001c0003t0001g0165a0001c0003t0001g0166 | 3 | HG02886.hp2 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.337-1184C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769241 | ||||||
chr19:17769274
|
C | CA | 49 | a0001c0001t0001g0104a0001c0001t0001g0151a0001c0001t0001g0153others(46): Show | 51 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.337-1131dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769274 | |||||
chr19:17769274
|
C | CAAAA | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(136): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.337-1134_337-1131d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769274 | |||||
chr19:17769274
|
C | CAAAAA | 42 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(39): Show | 42 | HG00438.hp1 HG00609.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.337-1135_337-1131d others(7): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769274 | |||||
chr19:17769274
|
CA | C | 34 | a0001c0001t0001g0180a0001c0004t0002g0002a0001c0004t0002g0003others(31): Show | 35 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.337-1131delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769274 | |||||
chr19:17769358
|
C | T | 20 | a0001c0001t0001g0193a0001c0001t0001g0214a0001c0001t0001g0220others(17): Show | 20 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.337-1067C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769358 | ||||||
chr19:17769425
|
G | A | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-1000G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769425 | ||||||
chr19:17769443
|
G | A | 1 | a0001c0002t0001g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.337-982G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769443 | ||||||
chr19:17769449
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.337-976G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769449 | ||||||
chr19:17769462
|
T | C | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(188): Show | 195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.337-963T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769462 | ||||||
chr19:17769495
|
C | T | 35 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(32): Show | 37 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.337-930C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769495 | ||||||
chr19:17769535
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.337-890C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769535 | ||||||
chr19:17769572
|
T | C | 226 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(223): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.337-853T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769572 | ||||||
chr19:17769579
|
AAACACAC others(10): Show |
A | 1 | a0001c0003t0001g0236 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.337-844_337-828del others(17): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769579 | |||||
chr19:17769580
|
AAC | A | 19 | a0001c0001t0001g0226a0001c0001t0001g0238a0001c0001t0001g0250others(16): Show | 19 | HG00609.hp2 HG00673.hp1 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.337-793_337-792del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACAC | A | 67 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0077others(64): Show | 69 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.337-795_337-792del others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACAC | A | 84 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0050others(81): Show | 86 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.337-797_337-792del others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACACA others(1): Show |
A | 26 | a0001c0001t0001g0053a0001c0001t0001g0071a0001c0001t0001g0072others(23): Show | 26 | HG01256.hp2 HG01261.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.337-799_337-792del others(8): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACACA others(3): Show |
A | 35 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0051others(32): Show | 36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.337-801_337-792del others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACACA others(5): Show |
A | 32 | a0001c0001t0001g0180a0001c0001t0001g0189a0001c0001t0001g0211others(29): Show | 32 | HG00140.hp1 HG01255.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.337-803_337-792del others(12): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACACA others(7): Show |
A | 14 | a0001c0001t0001g0167a0001c0002t0001g0085a0001c0003t0001g0016others(11): Show | 14 | HG00323.hp2 HG00733.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.337-805_337-792del others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACACA others(9): Show |
A | 32 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0151others(29): Show | 35 | HG00323.hp1 HG01070.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.337-807_337-792del others(16): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACACA others(11): Show |
A | 9 | a0001c0001t0001g0337a0001c0001t0001g0339a0001c0002t0001g0148others(6): Show | 9 | HG00140.hp2 HG00741.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-809_337-792del others(18): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACACA others(13): Show |
A | 10 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(7): Show | 11 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.337-811_337-792del others(20): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769580
|
AACACACA others(17): Show |
A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.337-815_337-792del others(24): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769580 | |||||
chr19:17769628
|
CACACA | C | 3 | a0001c0001t0001g0309a0001c0002t0006g0182a0001c0017t0001g0267 | 3 | HG00741.hp2 HG02055.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.337-795_337-791del others(5): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769628 | |||||
chr19:17769632
|
C | A | 1 | a0001c0005t0001g0112 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.337-793C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769632 | ||||||
chr19:17769638
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.337-787G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769638 | ||||||
chr19:17769652
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00099.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.337-773C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769652 | ||||||
chr19:17769688
|
G | C | 5 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-737G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769688 | ||||||
chr19:17769752
|
T | C | 1 | a0001c0001t0001g0334 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.337-673T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769752 | ||||||
chr19:17769819
|
T | G | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-606T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769819 | ||||||
chr19:17769839
|
C | CT | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(187): Show | 194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.337-578dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17769839 | |||||
chr19:17769890
|
G | A | 35 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(32): Show | 37 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.337-535G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769890 | ||||||
chr19:17769909
|
A | T | 35 | a0001c0001t0001g0151a0001c0001t0001g0153a0001c0002t0001g0148others(32): Show | 37 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.337-516A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769909 | ||||||
chr19:17769996
|
G | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.337-429G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17769996 | ||||||
chr19:17770021
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.337-404C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770021 | ||||||
chr19:17770318
|
A | AAC | 3 | a0001c0001t0001g0008a0001c0002t0002g0063a0001c0002t0002g0064 | 4 | HG00733.hp1 HG02109.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.337-93_337-92dupCA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr19 | 17770318 | |||||
chr19:17770332
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0001g0289 | 2 | HG01978.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.337-93C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770332 | ||||||
chr19:17770362
|
G | A | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.337-63G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770362 | ||||||
chr19:17770415
|
T | C | 5 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(2): Show | 5 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.337-10T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770415 | ||||||
chr19:17770421
|
G | A | 1 | a0001c0005t0001g0132 | 1 | HG01943.hp2 | splice_region_variant&intron_variant | LOW | c.337-4G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 7/28 | chr19 | 17770421 | ||||||
chr19:17770597
|
G | A | 2 | a0001c0001t0001g0339a0007c0014t0001g0049 | 2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.489+20G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770597 | ||||||
chr19:17770666
|
G | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02572.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.489+89G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770666 | ||||||
chr19:17770677
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.489+100C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770677 | ||||||
chr19:17770704
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.490-88C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770704 | ||||||
chr19:17770743
|
C | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.490-49C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770743 | ||||||
chr19:17770744
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.490-48C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 8/28 | chr19 | 17770744 | ||||||
chr19:17771025
|
G | A | 39 | a0001c0004t0001g0108a0001c0004t0001g0175a0001c0004t0002g0002others(36): Show | 40 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.594+129G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771025 | ||||||
chr19:17771130
|
G | T | 20 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 21 | HG01175.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.594+234G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771130 | ||||||
chr19:17771219
|
T | G | 1 | a0001c0002t0001g0086 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.594+323T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771219 | ||||||
chr19:17771237
|
G | A | 6 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+341G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771237 | ||||||
chr19:17771295
|
G | C | 11 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0050others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.594+399G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771295 | ||||||
chr19:17771309
|
T | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0058others(2): Show | 5 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+413T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771309 | ||||||
chr19:17771345
|
C | A | 1 | a0001c0002t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.594+449C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771345 | ||||||
chr19:17771358
|
T | TA | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047others(11): Show | 14 | HG01175.hp1 HG01496.hp2 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.594+474dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr19 | 17771358 | |||||
chr19:17771367
|
A | C | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG01243.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.594+471A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771367 | ||||||
chr19:17771370
|
AG | A | 49 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(46): Show | 51 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(48): Show |
intron_variant | MODIFIER | c.594+475delG | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771370 | ||||||
chr19:17771371
|
G | A | 225 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(222): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.594+475G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771371 | ||||||
chr19:17771387
|
G | C | 1 | a0001c0002t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.594+491G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771387 | ||||||
chr19:17771389
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.594+493C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771389 | ||||||
chr19:17771520
|
T | G | 2 | a0001c0001t0001g0297a0001c0001t0001g0342 | 2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.594+624T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771520 | ||||||
chr19:17771585
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.594+689C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771585 | ||||||
chr19:17771589
|
A | T | 1 | a0001c0001t0005g0195 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.594+693A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771589 | ||||||
chr19:17771605
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.594+709C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771605 | ||||||
chr19:17771626
|
G | A | 6 | a0001c0002t0001g0090a0001c0002t0001g0126a0001c0002t0001g0127others(3): Show | 6 | NA18963.hp1 NA18985.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+730G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771626 | ||||||
chr19:17771739
|
A | G | 154 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0062others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.595-718A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771739 | ||||||
chr19:17771874
|
G | A | 2 | a0001c0003t0001g0164a0001c0003t0001g0166 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.595-583G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17771874 | ||||||
chr19:17772003
|
G | T | 1 | a0001c0001t0001g0230 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.595-454G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772003 | ||||||
chr19:17772054
|
A | G | 276 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(273): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.595-403A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772054 | ||||||
chr19:17772113
|
T | C | 276 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(273): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.595-344T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772113 | ||||||
chr19:17772174
|
T | TTG | 3 | a0001c0001t0001g0226a0001c0001t0001g0328a0001c0001t0001g0329 | 3 | HG03834.hp2 NA18968.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.595-266_595-265dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr19 | 17772174 | |||||
chr19:17772174
|
TTG | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(164): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.595-266_595-265del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr19 | 17772174 | |||||
chr19:17772218
|
G | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047others(1): Show | 4 | HG01175.hp1 HG01496.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-239G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772218 | ||||||
chr19:17772264
|
A | G | 21 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(18): Show | 22 | HG01175.hp1 HG01496.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.595-193A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772264 | ||||||
chr19:17772266
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.595-191A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772266 | ||||||
chr19:17772425
|
C | G | 6 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-32C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 9/28 | chr19 | 17772425 | ||||||
chr19:17772630
|
G | A | 4 | a0001c0002t0002g0046a0001c0003t0002g0043a0001c0003t0002g0044others(1): Show | 4 | HG03688.hp2 HG04228.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-15G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 10/28 | chr19 | 17772630 | ||||||
chr19:17772818
|
AT | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0081a0001c0001t0001g0094others(10): Show | 14 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.790+87delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 17772818 | |||||
chr19:17772882
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.790+141C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17772882 | ||||||
chr19:17772955
|
A | T | 3 | a0001c0001t0001g0262a0001c0001t0001g0304a0001c0001t0001g0306 | 3 | HG00280.hp1 HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.790+214A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17772955 | ||||||
chr19:17772964
|
GGCCTTGG others(3): Show |
G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.790+224_790+233del others(10): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17772964 | ||||||
chr19:17773311
|
C | T | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(271): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.790+570C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773311 | ||||||
chr19:17773406
|
T | G | 1 | a0001c0009t0002g0333 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790+665T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773406 | ||||||
chr19:17773643
|
C | T | 1 | a0001c0001t0005g0195 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.791-596C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773643 | ||||||
chr19:17773764
|
G | T | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(194): Show | 201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.791-475G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773764 | ||||||
chr19:17773901
|
CTCT | C | 12 | a0001c0002t0001g0148a0001c0003t0001g0007a0001c0003t0001g0016others(9): Show | 13 | HG00323.hp2 HG01070.hp2 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.791-336_791-334del others(3): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 17773901 | |||||
chr19:17773903
|
CT | C | 44 | a0001c0001t0001g0247a0001c0001t0001g0249a0001c0001t0001g0253others(41): Show | 45 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.791-320delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 17773903 | |||||
chr19:17773903
|
CTT | C | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.791-321_791-320del others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr19 | 17773903 | |||||
chr19:17773904
|
T | TC | 23 | a0001c0002t0002g0046a0001c0002t0002g0063a0001c0002t0002g0064others(20): Show | 24 | HG00140.hp2 HG00741.hp1 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.791-335_791-334ins others(1): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773904 | ||||||
chr19:17773905
|
T | C | 3 | a0001c0001t0001g0271a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG03831.hp2 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.791-334T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773905 | ||||||
chr19:17773996
|
C | T | 1 | a0001c0002t0001g0138 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.791-243C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17773996 | ||||||
chr19:17774036
|
C | G | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.791-203C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17774036 | ||||||
chr19:17774072
|
G | A | 43 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.791-167G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 11/28 | chr19 | 17774072 | ||||||
chr19:17774499
|
G | A | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.920+21G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774499 | ||||||
chr19:17774516
|
A | C | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.920+38A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774516 | ||||||
chr19:17774527
|
C | T | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(271): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.920+49C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774527 | ||||||
chr19:17774730
|
G | A | 2 | a0001c0003t0001g0141a0001c0012t0001g0142 | 2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.920+252G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774730 | ||||||
chr19:17774846
|
C | A | 20 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(17): Show | 21 | HG01175.hp1 HG01496.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.921-210C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774846 | ||||||
chr19:17774890
|
A | G | 7 | a0001c0001t0001g0220a0001c0001t0001g0238a0001c0001t0001g0248others(4): Show | 7 | HG00609.hp2 HG00673.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.921-166A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17774890 | ||||||
chr19:17775019
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.921-37C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 13/28 | chr19 | 17775019 | ||||||
chr19:17775213
|
G | A | 5 | a0001c0003t0001g0165a0001c0007t0002g0139a0001c0007t0002g0332others(2): Show | 5 | HG01123.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+133G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 14/28 | chr19 | 17775213 | ||||||
chr19:17775253
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0310 | 2 | NA18965.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.945+173C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 14/28 | chr19 | 17775253 | ||||||
chr19:17775447
|
C | T | 1 | a0001c0006t0001g0179 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.946-9C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 14/28 | chr19 | 17775447 | ||||||
chr19:17775741
|
G | T | 3 | a0001c0001t0001g0262a0001c0001t0001g0304a0001c0001t0001g0306 | 3 | HG00280.hp1 HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1003+228G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775741 | ||||||
chr19:17775810
|
G | C | 6 | a0001c0001t0001g0178a0001c0001t0001g0215a0001c0001t0001g0217others(3): Show | 6 | HG03490.hp1 HG03491.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.1004-173G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775810 | ||||||
chr19:17775857
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1004-126G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775857 | ||||||
chr19:17775885
|
C | T | 1 | a0001c0011t0002g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1004-98C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775885 | ||||||
chr19:17775943
|
G | A | 17 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(14): Show | 17 | HG00544.hp2 HG01192.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.1004-40G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 15/28 | chr19 | 17775943 | ||||||
chr19:17776181
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1182+20C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 16/28 | chr19 | 17776181 | ||||||
chr19:17776215
|
T | C | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(271): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1183-32T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 16/28 | chr19 | 17776215 | ||||||
chr19:17776235
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-12C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 16/28 | chr19 | 17776235 | ||||||
chr19:17776511
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1208-124C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 17/28 | chr19 | 17776511 | ||||||
chr19:17776550
|
C | T | 1 | a0001c0002t0001g0110 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1208-85C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 17/28 | chr19 | 17776550 | ||||||
chr19:17776754
|
G | A | 76 | a0001c0002t0001g0148a0001c0002t0002g0046a0001c0002t0002g0063others(73): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1259+68G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17776754 | ||||||
chr19:17776799
|
G | GT | 11 | a0001c0001t0001g0068a0001c0001t0001g0196a0001c0001t0001g0305others(8): Show | 11 | HG01934.hp1 HG02559.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1259+120dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17776799 | |||||
chr19:17776999
|
T | C | 2 | a0001c0003t0001g0164a0001c0003t0001g0166 | 2 | HG02886.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1259+313T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17776999 | ||||||
chr19:17777061
|
G | T | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1259+375G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777061 | ||||||
chr19:17777067
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1259+381G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777067 | ||||||
chr19:17777177
|
T | A | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+491T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777177 | ||||||
chr19:17777179
|
G | T | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+493G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777179 | ||||||
chr19:17777181
|
G | T | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+495G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777181 | ||||||
chr19:17777185
|
G | C | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+499G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777185 | ||||||
chr19:17777186
|
G | A | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+500G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777186 | ||||||
chr19:17777188
|
T | G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+502T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777188 | ||||||
chr19:17777201
|
C | G | 6 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1259+515C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777201 | ||||||
chr19:17777226
|
T | G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+540T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777226 | ||||||
chr19:17777227
|
G | T | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+541G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777227 | ||||||
chr19:17777228
|
A | C | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+542A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777228 | ||||||
chr19:17777237
|
T | A | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+551T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777237 | ||||||
chr19:17777245
|
T | C | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+559T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777245 | ||||||
chr19:17777263
|
G | C | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+577G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777263 | ||||||
chr19:17777264
|
T | A | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+578T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777264 | ||||||
chr19:17777265
|
G | A | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+579G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777265 | ||||||
chr19:17777297
|
G | A | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+611G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777297 | ||||||
chr19:17777303
|
A | G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+617A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777303 | ||||||
chr19:17777308
|
A | T | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+622A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777308 | ||||||
chr19:17777311
|
C | G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+625C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777311 | ||||||
chr19:17777312
|
G | C | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+626G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777312 | ||||||
chr19:17777327
|
G | A | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+641G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777327 | ||||||
chr19:17777328
|
A | G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+642A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777328 | ||||||
chr19:17777345
|
T | G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+659T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777345 | ||||||
chr19:17777355
|
A | G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+669A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777355 | ||||||
chr19:17777366
|
A | G | 1 | a0004c0019t0001g0324 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1259+680A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777366 | ||||||
chr19:17777405
|
A | G | 274 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(271): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1259+719A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777405 | ||||||
chr19:17777512
|
G | A | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(195): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.1260-625G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777512 | ||||||
chr19:17777535
|
CA | C | 91 | a0001c0002t0001g0054a0001c0002t0001g0055a0001c0002t0001g0078others(88): Show | 94 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.1260-575delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | |||||
chr19:17777535
|
CAAA | C | 25 | a0001c0001t0001g0062a0001c0001t0001g0111a0001c0001t0001g0196others(22): Show | 25 | HG01358.hp2 HG01928.hp2 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.1260-577_1260-575d others(5): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | |||||
chr19:17777535
|
CAAAA | C | 144 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(141): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1260-578_1260-575d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | |||||
chr19:17777535
|
CAAAAA | C | 15 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 16 | HG01175.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1260-579_1260-575d others(7): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | |||||
chr19:17777535
|
CAAAAAA | C | 13 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(10): Show | 13 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1260-580_1260-575d others(8): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17777535 | |||||
chr19:17777551
|
A | G | 73 | a0001c0002t0001g0148a0001c0002t0002g0046a0001c0002t0002g0063others(70): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.1260-586A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777551 | ||||||
chr19:17777845
|
G | C | 268 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(265): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1260-292G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777845 | ||||||
chr19:17777854
|
C | A | 1 | a0001c0001t0001g0284 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1260-283C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777854 | ||||||
chr19:17777970
|
C | T | 1 | a0001c0001t0005g0263 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1260-167C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777970 | ||||||
chr19:17777978
|
G | A | 172 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(169): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1260-159G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777978 | ||||||
chr19:17777986
|
C | T | 1 | a0001c0002t0002g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1260-151C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17777986 | ||||||
chr19:17778017
|
C | T | 1 | a0001c0002t0001g0085 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1260-120C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | chr19 | 17778017 | ||||||
chr19:17778038
|
C | CA | 76 | a0001c0001t0001g0057a0001c0002t0001g0148a0001c0002t0002g0046others(73): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1260-87dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr19 | 17778038 | |||||
chr19:17778235
|
G | A | 29 | a0001c0002t0001g0148a0001c0003t0001g0006a0001c0003t0001g0007others(26): Show | 31 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(28): Show |
splice_region_variant&intron_variant | LOW | c.1351+7G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 19/28 | chr19 | 17778235 | ||||||
chr19:17778350
|
A | G | 1 | a0001c0004t0003g0022 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1351+122A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 19/28 | chr19 | 17778350 | ||||||
chr19:17778977
|
G | C | 4 | a0001c0002t0002g0063a0001c0002t0002g0064a0001c0003t0001g0164others(1): Show | 4 | HG02109.hp1 HG02886.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+93G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17778977 | ||||||
chr19:17779036
|
G | A | 1 | a0001c0012t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1627+152G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779036 | ||||||
chr19:17779054
|
C | CG | 38 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0151others(35): Show | 38 | HG00609.hp2 HG01175.hp2 HG01891.hp2 others(35): Show |
intron_variant | MODIFIER | c.1627+172dupG | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779054 | |||||
chr19:17779269
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1627+385A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779269 | ||||||
chr19:17779270
|
A | G | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(261): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1627+386A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779270 | ||||||
chr19:17779378
|
T | C | 5 | a0001c0003t0001g0165a0001c0007t0002g0139a0001c0007t0002g0332others(2): Show | 5 | HG01123.hp2 HG02258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627+494T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779378 | ||||||
chr19:17779382
|
G | A | 1 | a0001c0003t0001g0152 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1627+498G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779382 | ||||||
chr19:17779506
|
G | A | 3 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0047 | 3 | HG01175.hp1 HG01496.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1627+622G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779506 | ||||||
chr19:17779515
|
G | T | 1 | a0005c0018t0001g0298 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1627+631G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779515 | ||||||
chr19:17779545
|
A | G | 268 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(265): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1627+661A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779545 | ||||||
chr19:17779613
|
A | AGCGGAGT others(327): Show |
2 | a0001c0003t0001g0141a0001c0012t0001g0142 | 2 | HG02809.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1627+763_1627+764i others(336): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779613 | |||||
chr19:17779613
|
AGCGGAGT others(27): Show |
A | 24 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(21): Show | 25 | HG01123.hp2 HG01175.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1627+764_1627+797d others(36): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779613 | |||||
chr19:17779625
|
G | GGAGGGAG others(89): Show |
1 | a0001c0005t0001g0118 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1627+742_1627+837d others(98): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779625 | |||||
chr19:17779648
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1627+764G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779648 | ||||||
chr19:17779651
|
G | GAGTCAAG others(25): Show |
1 | a0001c0001t0001g0337 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1627+798_1627+829d others(34): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779651 | |||||
chr19:17779721
|
CAAGG | C | 155 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0062others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1627+838_1627+841d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17779721 | ||||||
chr19:17779952
|
T | TG | 34 | a0001c0001t0001g0051a0001c0001t0001g0057a0001c0001t0001g0084others(31): Show | 34 | HG00544.hp2 HG01099.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1627+1074dupG | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17779952 | |||||
chr19:17780011
|
G | A | 159 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0062others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1627+1127G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780011 | ||||||
chr19:17780156
|
A | C | 1 | a0001c0003t0004g0145 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1628-1075A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780156 | ||||||
chr19:17780161
|
C | CT | 227 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1628-1050dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17780161 | |||||
chr19:17780161
|
C | CTT | 14 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0151others(11): Show | 14 | HG00140.hp2 HG00741.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-1051_1628-105 others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | INFO_REALIGN_3_PRIME | chr19 | 17780161 | |||||
chr19:17780161
|
C | T | 1 | a0001c0005t0001g0113 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1628-1070C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780161 | ||||||
chr19:17780207
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1628-1024C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780207 | ||||||
chr19:17780208
|
G | A | 1 | a0001c0003t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1628-1023G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780208 | ||||||
chr19:17780272
|
T | C | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(261): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1628-959T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780272 | ||||||
chr19:17780323
|
G | A | 2 | a0001c0007t0002g0332a0001c0007t0003g0331 | 2 | HG01123.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1628-908G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780323 | ||||||
chr19:17780453
|
C | T | 1 | a0001c0012t0001g0142 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1628-778C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780453 | ||||||
chr19:17780567
|
C | G | 1 | a0001c0001t0001g0201 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1628-664C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780567 | ||||||
chr19:17780687
|
C | T | 3 | a0001c0002t0001g0085a0001c0002t0001g0087a0001c0002t0001g0095 | 3 | HG03516.hp2 NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-544C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780687 | ||||||
chr19:17780750
|
T | G | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(261): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1628-481T>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780750 | ||||||
chr19:17780959
|
C | T | 2 | a0001c0003t0001g0154a0001c0003t0004g0146 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1628-272C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 20/28 | chr19 | 17780959 | ||||||
chr19:17781356
|
G | A | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1740+13G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 21/28 | chr19 | 17781356 | ||||||
chr19:17781357
|
C | A | 2 | a0001c0002t0002g0063a0001c0002t0002g0064 | 2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1740+14C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 21/28 | chr19 | 17781357 | ||||||
chr19:17781384
|
G | C | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(264): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1740+41G>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 21/28 | chr19 | 17781384 | ||||||
chr19:17781564
|
G | A | 15 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0081others(12): Show | 16 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1828+25G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 22/28 | chr19 | 17781564 | ||||||
chr19:17781635
|
C | T | 7 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0003t0001g0165others(4): Show | 7 | HG01123.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1829-77C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 22/28 | chr19 | 17781635 | ||||||
chr19:17781669
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(264): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1829-43A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 22/28 | chr19 | 17781669 | ||||||
chr19:17781680
|
G | T | 1 | a0001c0001t0001g0167 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1829-32G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 22/28 | chr19 | 17781680 | ||||||
chr19:17781897
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1937+77C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17781897 | ||||||
chr19:17781987
|
CT | C | 62 | a0001c0001t0001g0011a0001c0001t0001g0051a0001c0002t0001g0054others(59): Show | 64 | HG00639.hp2 HG01069.hp2 HG01167.hp1 others(61): Show |
intron_variant | MODIFIER | c.1937+196delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | |||||
chr19:17781987
|
CTT | C | 35 | a0001c0001t0001g0047a0001c0001t0001g0052a0001c0003t0001g0165others(32): Show | 36 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.1937+195_1937+196d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | |||||
chr19:17781987
|
CTTTT | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0050others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1937+193_1937+196d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | |||||
chr19:17781987
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0214a0001c0001t0001g0221 | 2 | HG01981.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1937+182_1937+196d others(17): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | |||||
chr19:17781987
|
CTTTTTTT others(9): Show |
C | 205 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(202): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1937+181_1937+196d others(18): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr19 | 17781987 | |||||
chr19:17782071
|
G | A | 219 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(216): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.1937+251G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782071 | ||||||
chr19:17782103
|
G | A | 6 | a0001c0006t0001g0168a0001c0006t0001g0169a0001c0006t0001g0170others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1937+283G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782103 | ||||||
chr19:17782328
|
G | A | 60 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 62 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1937+508G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782328 | ||||||
chr19:17782371
|
A | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 6 | HG01891.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1937+551A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782371 | ||||||
chr19:17782528
|
A | G | 2 | a0001c0003t0001g0159a0001c0003t0004g0145 | 2 | HG01517.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1938-489A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782528 | ||||||
chr19:17782565
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(264): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1938-452A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782565 | ||||||
chr19:17782679
|
A | C | 28 | a0001c0003t0001g0006a0001c0003t0001g0007a0001c0003t0001g0016others(25): Show | 30 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.1938-338A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782679 | ||||||
chr19:17782793
|
A | G | 60 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 62 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.1938-224A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782793 | ||||||
chr19:17782814
|
T | A | 1 | a0001c0001t0001g0214 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1938-203T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 23/28 | chr19 | 17782814 | ||||||
chr19:17783185
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0001g0181a0001c0001t0001g0183others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2093+13G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783185 | ||||||
chr19:17783247
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2093+75C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783247 | ||||||
chr19:17783259
|
A | AT | 44 | a0001c0001t0001g0005a0001c0001t0001g0067a0001c0001t0001g0081others(41): Show | 46 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.2093+93dupT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 17783259 | |||||
chr19:17783259
|
A | ATT | 3 | a0001c0003t0001g0006a0001c0003t0001g0156a0001c0003t0001g0204 | 4 | HG01167.hp2 HG02738.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2093+92_2093+93dup others(2): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | INFO_REALIGN_3_PRIME | chr19 | 17783259 | |||||
chr19:17783266
|
C | T | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(264): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.2093+94C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783266 | ||||||
chr19:17783271
|
C | T | 1 | a0001c0003t0002g0045 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2093+99C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783271 | ||||||
chr19:17783441
|
G | A | 2 | a0001c0002t0006g0182a0001c0002t0006g0188 | 2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2093+269G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783441 | ||||||
chr19:17783460
|
G | A | 1 | a0001c0001t0001g0296 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2093+288G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783460 | ||||||
chr19:17783488
|
A | G | 269 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(266): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.2093+316A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783488 | ||||||
chr19:17783506
|
A | G | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2093+334A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783506 | ||||||
chr19:17783563
|
C | T | 3 | a0001c0002t0001g0176a0001c0002t0001g0242a0001c0002t0001g0257 | 3 | HG01256.hp2 HG02273.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2093+391C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17783563 | ||||||
chr19:17784032
|
G | T | 1 | a0001c0001t0001g0256 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2094-71G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17784032 | ||||||
chr19:17784069
|
C | T | 39 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0050others(36): Show | 41 | HG00140.hp2 HG00323.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.2094-34C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 24/28 | chr19 | 17784069 | ||||||
chr19:17784413
|
C | T | 1 | a0001c0002t0001g0120 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2226+178C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784413 | ||||||
chr19:17784442
|
G | A | 267 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(264): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.2226+207G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784442 | ||||||
chr19:17784471
|
A | C | 227 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(224): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.2226+236A>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784471 | ||||||
chr19:17784550
|
C | T | 1 | a0001c0001t0001g0326 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2227-175C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784550 | ||||||
chr19:17784631
|
G | A | 2 | a0001c0002t0001g0242a0001c0003t0001g0141 | 2 | HG02273.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2227-94G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 25/28 | chr19 | 17784631 | ||||||
chr19:17784981
|
C | A | 3 | a0001c0001t0001g0339a0001c0002t0002g0063a0001c0002t0002g0064 | 3 | HG02109.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2426+57C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17784981 | ||||||
chr19:17785017
|
G | A | 34 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0059others(31): Show | 34 | HG00280.hp1 HG00609.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2426+93G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785017 | ||||||
chr19:17785065
|
G | A | 126 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0010others(123): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.2426+141G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785065 | ||||||
chr19:17785242
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2426+318T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785242 | ||||||
chr19:17785341
|
C | G | 1 | a0001c0001t0001g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2426+417C>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785341 | ||||||
chr19:17785423
|
A | G | 6 | a0001c0002t0001g0090a0001c0002t0001g0126a0001c0002t0001g0127others(3): Show | 6 | NA18963.hp1 NA18985.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426+499A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785423 | ||||||
chr19:17785483
|
A | G | 37 | a0001c0001t0001g0051a0001c0001t0001g0074a0001c0001t0001g0206others(34): Show | 38 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.2426+559A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785483 | ||||||
chr19:17785518
|
C | T | 1 | a0001c0003t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2426+594C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785518 | ||||||
chr19:17785533
|
AT | A | 6 | a0001c0001t0001g0074a0001c0002t0001g0092a0001c0002t0001g0093others(3): Show | 6 | HG02615.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2426+610delT | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785533 | ||||||
chr19:17785555
|
C | T | 6 | a0001c0002t0001g0089a0001c0002t0001g0119a0001c0002t0001g0120others(3): Show | 6 | NA18945.hp2 NA18957.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426+631C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785555 | ||||||
chr19:17785556
|
G | A | 1 | a0001c0016t0001g0232 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2426+632G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785556 | ||||||
chr19:17785562
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2426+638G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785562 | ||||||
chr19:17785615
|
C | T | 4 | a0001c0001t0001g0269a0001c0003t0001g0154a0001c0003t0004g0146others(1): Show | 4 | HG01168.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426+691C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785615 | ||||||
chr19:17785636
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2426+712A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785636 | ||||||
chr19:17785753
|
G | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0077a0001c0001t0001g0183others(3): Show | 6 | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2427-821G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785753 | ||||||
chr19:17785833
|
C | CA | 94 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0052others(91): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.2427-726dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17785833 | |||||
chr19:17785833
|
C | CAA | 32 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0065others(29): Show | 33 | HG00733.hp2 HG01168.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.2427-727_2427-726d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17785833 | |||||
chr19:17785833
|
C | CAAA | 10 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0048others(7): Show | 10 | HG01981.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2427-728_2427-726d others(5): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17785833 | |||||
chr19:17785833
|
CA | C | 7 | a0001c0001t0001g0196a0001c0001t0001g0256a0001c0001t0001g0287others(4): Show | 7 | HG01257.hp2 HG01975.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.2427-726delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17785833 | |||||
chr19:17785935
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2427-639G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785935 | ||||||
chr19:17785978
|
T | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 41 | HG00733.hp2 HG01168.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.2427-596T>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785978 | ||||||
chr19:17785979
|
A | T | 57 | a0001c0001t0001g0051a0001c0001t0001g0074a0001c0001t0001g0167others(54): Show | 59 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.2427-595A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785979 | ||||||
chr19:17785980
|
A | T | 1 | a0001c0003t0001g0149 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2427-594A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17785980 | ||||||
chr19:17786016
|
T | C | 24 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0284others(21): Show | 26 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.2427-558T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17786016 | ||||||
chr19:17786048
|
A | G | 1 | a0001c0007t0002g0139 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2427-526A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17786048 | ||||||
chr19:17786091
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2427-483T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17786091 | ||||||
chr19:17786331
|
TCAAAAAA others(5): Show |
T | 29 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0067others(26): Show | 30 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.2427-230_2427-219d others(14): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17786331 | |||||
chr19:17786361
|
A | AAC | 3 | a0001c0001t0001g0276a0001c0001t0001g0279a0001c0001t0001g0286 | 3 | HG03017.hp1 NA19091.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2427-191_2427-190d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17786361 | |||||
chr19:17786361
|
AAC | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(65): Show | 71 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.2427-191_2427-190d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17786361 | |||||
chr19:17786361
|
AACAC | A | 3 | a0001c0002t0002g0063a0001c0002t0002g0064a0010c0010t0002g0140 | 3 | HG02109.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2427-193_2427-190d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr19 | 17786361 | |||||
chr19:17786461
|
A | T | 1 | a0001c0002t0001g0148 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2427-113A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 26/28 | chr19 | 17786461 | ||||||
chr19:17787175
|
G | T | 1 | a0001c0003t0001g0141 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2483-507G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787175 | ||||||
chr19:17787187
|
G | A | 34 | a0001c0001t0001g0051a0001c0001t0001g0074a0001c0001t0001g0206others(31): Show | 35 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2483-495G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787187 | ||||||
chr19:17787223
|
C | CA | 65 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0076others(62): Show | 65 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2483-429dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | |||||
chr19:17787223
|
C | CAA | 15 | a0001c0001t0001g0070a0001c0001t0001g0073a0001c0001t0001g0082others(12): Show | 15 | HG00280.hp1 HG00423.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.2483-430_2483-429d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | |||||
chr19:17787223
|
CA | C | 8 | a0001c0001t0001g0153a0001c0001t0001g0266a0001c0001t0001g0288others(5): Show | 8 | HG00323.hp1 HG02040.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2483-429delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | |||||
chr19:17787223
|
CAA | C | 14 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(11): Show | 15 | HG01175.hp1 HG01891.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.2483-430_2483-429d others(4): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | |||||
chr19:17787223
|
CAAA | C | 67 | a0001c0001t0001g0025a0001c0001t0001g0048a0001c0001t0001g0050others(64): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.2483-431_2483-429d others(5): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | |||||
chr19:17787223
|
CAAAA | C | 6 | a0001c0001t0001g0269a0001c0002t0001g0085a0001c0002t0001g0095others(3): Show | 6 | HG01168.hp2 HG01256.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2483-432_2483-429d others(6): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | |||||
chr19:17787223
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2483-438_2483-429d others(12): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | |||||
chr19:17787223
|
CAAAAAAA others(4): Show |
C | 28 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0067others(25): Show | 29 | HG00738.hp1 HG00741.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2483-439_2483-429d others(13): Show |
FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787223 | |||||
chr19:17787242
|
A | T | 1 | a0001c0001t0001g0280 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2483-440A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787242 | ||||||
chr19:17787402
|
C | A | 1 | a0001c0001t0001g0051 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2483-280C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787402 | ||||||
chr19:17787411
|
T | TA | 42 | a0001c0001t0001g0005a0001c0001t0001g0052a0001c0001t0001g0067others(39): Show | 43 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.2483-254dupA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787411 | |||||
chr19:17787411
|
TA | T | 7 | a0001c0001t0001g0069a0001c0001t0001g0075a0001c0001t0001g0275others(4): Show | 7 | HG01099.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2483-254delA | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr19 | 17787411 | |||||
chr19:17787412
|
A | G | 2 | a0001c0001t0001g0328a0001c0002t0001g0096 | 2 | HG02622.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2483-270A>G | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787412 | ||||||
chr19:17787658
|
G | A | 6 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(3): Show | 7 | HG01891.hp1 HG02280.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2483-24G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 27/28 | chr19 | 17787658 | ||||||
chr19:17787908
|
G | A | 27 | a0001c0001t0001g0075a0001c0001t0001g0209a0001c0001t0001g0210others(24): Show | 29 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2647+62G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17787908 | ||||||
chr19:17787953
|
G | A | 1 | a0001c0003t0001g0204 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2647+107G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17787953 | ||||||
chr19:17787981
|
A | T | 9 | a0001c0003t0007g0147a0001c0003t0007g0161a0001c0004t0003g0017others(6): Show | 9 | HG00733.hp2 HG01884.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2647+135A>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17787981 | ||||||
chr19:17788077
|
G | T | 3 | a0001c0001t0001g0217a0001c0001t0001g0258a0001c0002t0001g0109 | 3 | HG03491.hp2 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2648-207G>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788077 | ||||||
chr19:17788221
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2648-63G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788221 | ||||||
chr19:17788238
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2648-46G>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788238 | ||||||
chr19:17788242
|
C | T | 1 | a0001c0001t0001g0340 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2648-42C>T | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788242 | ||||||
chr19:17788271
|
T | C | 3 | a0001c0004t0003g0017a0001c0004t0003g0018a0001c0007t0003g0331 | 3 | HG01884.hp2 HG02258.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2648-13T>C | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788271 | ||||||
chr19:17788277
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | splice_region_variant&intron_variant | LOW | c.2648-7C>A | FCHO1 | ENSG00000130475.16 | transcript | ENST00000596536.6 | protein_coding | 28/28 | chr19 | 17788277 |