geneid | 2346 |
---|---|
ensemblid | ENSG00000086205.18 |
hgncid | 3788 |
symbol | FOLH1 |
name | folate hydrolase 1 |
refseq_nuc | NM_004476.3 |
refseq_prot | NP_004467.1 |
ensembl_nuc | ENST00000256999.7 |
ensembl_prot | ENSP00000256999.2 |
mane_status | MANE Select |
chr | chr11 |
start | 49145092 |
end | 49208602 |
strand | - |
ver | v1.2 |
region | chr11:49145092-49208602 |
region5000 | chr11:49140092-49213602 |
regionname0 | FOLH1_chr11_49145092_49208602 |
regionname5000 | FOLH1_chr11_49140092_49213602 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 750 | 195 | 35 | 39 | 92 | 11 | 17 | 70 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002 | 0/1 | 750 | 166 | 50 | 21 | 74 | 5 | 15 | 56 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0003 | 0/0 | 749 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0004 | 0/0 | 750 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0005 | 0/0 | 750 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2253 | 184 | 27 | 37 | 92 | 11 | 16 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0002 | 0/1 | 2253 | 99 | 50 | 11 | 33 | 0 | 4 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0003 | 0/0 | 2253 | 66 | 0 | 9 | 41 | 5 | 11 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0004 | 0/0 | 2253 | 8 | 8 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0005 | 0/0 | 2250 | 6 | 5 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0006 | 0/0 | 2253 | 5 | 5 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0007 | 0/0 | 2253 | 2 | 1 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0008 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0009 | 0/0 | 2253 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0010 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
c0011 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1858 | 139 | 45 | 18 | 54 | 8 | 13 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0002 | 0/0 | 1858 | 138 | 15 | 29 | 75 | 5 | 14 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0003 | 0/1 | 1858 | 66 | 19 | 11 | 33 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0004 | 0/0 | 1858 | 6 | 6 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0005 | 0/0 | 1858 | 5 | 0 | 3 | 0 | 2 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0006 | 0/0 | 1858 | 4 | 4 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0007 | 0/0 | 1858 | 3 | 3 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0008 | 0/0 | 1858 | 3 | 1 | 0 | 0 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0009 | 0/0 | 1858 | 2 | 1 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0010 | 0/0 | 1858 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0011 | 0/0 | 1858 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0012 | 0/0 | 1858 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0013 | 0/0 | 1858 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0014 | 0/0 | 1858 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0015 | 0/0 | 1858 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
t0016 | 0/0 | 1858 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
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 | 9 | 0 | 0 | 9 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0009 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2253 | 184 | 27 | 37 | 92 | 11 | 16 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0004 | 0/0 | 2253 | 8 | 8 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0008 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0009 | 0/0 | 2253 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0010 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0002 | 0/1 | 2253 | 99 | 50 | 11 | 33 | 0 | 4 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0003 | 0/0 | 2253 | 66 | 0 | 9 | 41 | 5 | 11 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0011 | 0/0 | 2253 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0003c0005 | 0/0 | 2250 | 6 | 5 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0004c0006 | 0/0 | 2253 | 5 | 5 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0005c0007 | 0/0 | 2253 | 2 | 1 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4110 | 40 | 11 | 8 | 14 | 4 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0001t0002 | 0/0 | 4110 | 131 | 13 | 26 | 75 | 4 | 13 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0001t0005 | 0/0 | 4110 | 5 | 0 | 3 | 0 | 2 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0001t0007 | 0/0 | 4110 | 3 | 3 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0001t0011 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0001t0012 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0001t0014 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0001t0015 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0001t0016 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0004t0001 | 0/0 | 4110 | 8 | 8 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0008t0002 | 0/0 | 4110 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0009t0002 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0001c0010t0002 | 0/0 | 4110 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0002t0001 | 0/0 | 4110 | 26 | 26 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0002t0002 | 0/0 | 4110 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0002t0003 | 0/1 | 4110 | 66 | 19 | 11 | 33 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0002t0004 | 0/0 | 4110 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0002t0008 | 0/0 | 4110 | 3 | 1 | 0 | 0 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0002t0010 | 0/0 | 4110 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0003t0001 | 0/0 | 4110 | 64 | 0 | 9 | 40 | 4 | 11 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0003t0002 | 0/0 | 4110 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0003t0013 | 0/0 | 4110 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0002c0011t0001 | 0/0 | 4110 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0003c0005t0002 | 0/0 | 4107 | 2 | 1 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0003c0005t0006 | 0/0 | 4107 | 4 | 4 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0004c0006t0004 | 0/0 | 4110 | 5 | 5 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
a0005c0007t0009 | 0/0 | 4110 | 2 | 1 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | copy fasta | chr11 | 49140092 | 49213602 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0007g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0014g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0015g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0001t0016g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0004t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0004t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0008t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0009t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0001c0010t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0001 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0008g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0008g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0002t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0003t0013g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0002c0011t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0003c0005t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0003c0005t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0003c0005t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0003c0005t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0003c0005t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0004c0006t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0004c0006t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0004c0006t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0004c0006t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0005c0007t0009g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
a0005c0007t0009g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0212 | EUR | GBR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0062 | EUR | GBR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00140 | hp2 | a0001 | c0001 | t0005 | g0170 | EUR | GBR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0144 | EUR | FIN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00408 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00423 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00544 | hp2 | a0002 | c0003 | t0001 | g0085 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00558 | hp2 | a0002 | c0002 | t0003 | g0281 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00597 | hp1 | a0002 | c0003 | t0001 | g0052 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00597 | hp2 | a0002 | c0002 | t0003 | g0287 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00609 | hp1 | a0002 | c0002 | t0003 | g0272 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00609 | hp2 | a0002 | c0003 | t0001 | g0057 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0065 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00733 | hp1 | a0002 | c0002 | t0003 | g0283 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00733 | hp2 | a0002 | c0003 | t0001 | g0084 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0033 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01081 | hp2 | a0002 | c0002 | t0003 | g0011 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01099 | hp2 | a0002 | c0003 | t0001 | g0054 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01109 | hp1 | a0003 | c0005 | t0002 | g0030 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01109 | hp2 | a0002 | c0011 | t0001 | g0312 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01168 | hp1 | a0001 | c0008 | t0002 | g0213 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01175 | hp2 | a0001 | c0010 | t0002 | g0210 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0252 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01255 | hp1 | a0002 | c0002 | t0003 | g0011 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01257 | hp1 | a0002 | c0002 | t0003 | g0304 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0097 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01346 | hp1 | a0002 | c0002 | t0003 | g0024 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01346 | hp2 | a0005 | c0007 | t0009 | g0243 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01358 | hp1 | a0002 | c0002 | t0003 | g0024 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01361 | hp1 | a0002 | c0003 | t0001 | g0070 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01433 | hp1 | a0002 | c0003 | t0001 | g0073 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0204 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01496 | hp1 | a0002 | c0002 | t0003 | g0266 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01515 | hp2 | a0001 | c0001 | t0015 | g0324 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0201 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0064 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01517 | hp1 | a0002 | c0003 | t0001 | g0061 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01884 | hp1 | a0003 | c0005 | t0006 | g0028 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0300 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01952 | hp2 | a0002 | c0003 | t0001 | g0071 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01978 | hp1 | a0002 | c0002 | t0003 | g0284 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01978 | hp2 | a0002 | c0003 | t0001 | g0086 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01993 | hp1 | a0002 | c0003 | t0001 | g0068 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02040 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02040 | hp2 | a0002 | c0002 | t0003 | g0271 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02055 | hp1 | a0003 | c0005 | t0006 | g0327 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02056 | hp2 | a0002 | c0002 | t0003 | g0259 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02074 | hp1 | a0002 | c0002 | t0003 | g0285 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02135 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02135 | hp2 | a0001 | c0001 | t0014 | g0180 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0315 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | CDX | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02155 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | CDX | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CDX | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02165 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | CDX | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02258 | hp1 | a0002 | c0002 | t0003 | g0254 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02273 | hp1 | a0002 | c0002 | t0003 | g0011 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02293 | hp1 | a0002 | c0003 | t0001 | g0069 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0314 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02451 | hp2 | a0002 | c0002 | t0003 | g0299 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02602 | hp1 | a0002 | c0003 | t0001 | g0032 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02602 | hp2 | a0001 | c0009 | t0002 | g0169 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02615 | hp1 | a0004 | c0006 | t0004 | g0318 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02615 | hp2 | a0002 | c0002 | t0003 | g0022 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02622 | hp1 | a0004 | c0006 | t0004 | g0026 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0102 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02647 | hp1 | a0002 | c0002 | t0003 | g0248 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0291 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02698 | hp1 | a0002 | c0002 | t0008 | g0258 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0034 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02717 | hp2 | a0004 | c0006 | t0004 | g0026 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0309 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02738 | hp2 | a0002 | c0003 | t0001 | g0072 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0112 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02818 | hp1 | a0002 | c0002 | t0003 | g0261 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0245 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02886 | hp1 | a0002 | c0002 | t0003 | g0267 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02886 | hp2 | a0002 | c0002 | t0003 | g0251 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0108 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0298 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0257 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02897 | hp1 | a0002 | c0002 | t0003 | g0256 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02897 | hp2 | a0001 | c0004 | t0001 | g0111 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0307 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0306 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02970 | hp1 | a0002 | c0002 | t0003 | g0021 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02976 | hp1 | a0003 | c0005 | t0002 | g0029 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03017 | hp1 | a0002 | c0003 | t0001 | g0260 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0292 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0316 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0308 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0305 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03209 | hp1 | a0002 | c0002 | t0003 | g0297 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0301 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0021 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0063 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03453 | hp2 | a0004 | c0006 | t0004 | g0320 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0311 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0255 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03491 | hp1 | a0002 | c0003 | t0001 | g0013 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0262 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03492 | hp1 | a0002 | c0003 | t0001 | g0013 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03492 | hp2 | a0002 | c0002 | t0008 | g0275 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03516 | hp1 | a0002 | c0002 | t0003 | g0253 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0310 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0198 | AFR | GWD | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03579 | hp1 | a0002 | c0002 | t0004 | g0313 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0199 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0059 | SAS | PJL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0277 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03834 | hp2 | a0002 | c0003 | t0001 | g0058 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03942 | hp2 | a0001 | c0001 | t0012 | g0184 | SAS | BEB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0103 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG04115 | hp2 | a0002 | c0003 | t0001 | g0074 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG04199 | hp1 | a0002 | c0003 | t0001 | g0075 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | STU | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18522 | hp1 | a0002 | c0002 | t0010 | g0249 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0109 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | CHB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18906 | hp2 | a0002 | c0002 | t0003 | g0022 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18939 | hp1 | a0002 | c0003 | t0013 | g0046 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18940 | hp1 | a0002 | c0002 | t0003 | g0286 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0282 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0041 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18944 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18944 | hp2 | a0002 | c0002 | t0003 | g0270 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18945 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18946 | hp1 | a0002 | c0002 | t0003 | g0278 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18947 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18948 | hp2 | a0002 | c0003 | t0001 | g0081 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18951 | hp2 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18953 | hp1 | a0002 | c0002 | t0003 | g0274 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18954 | hp1 | a0002 | c0002 | t0003 | g0269 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18954 | hp2 | a0002 | c0003 | t0001 | g0051 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18956 | hp2 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18959 | hp1 | a0002 | c0002 | t0003 | g0276 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0050 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18962 | hp2 | a0002 | c0003 | t0001 | g0053 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18965 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18970 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18975 | hp1 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18977 | hp1 | a0002 | c0002 | t0003 | g0288 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18978 | hp2 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18981 | hp1 | a0002 | c0002 | t0003 | g0280 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18981 | hp2 | a0002 | c0003 | t0001 | g0083 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18982 | hp1 | a0002 | c0002 | t0003 | g0012 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18986 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18986 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18987 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18990 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18991 | hp1 | a0001 | c0001 | t0011 | g0142 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18993 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18999 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19001 | hp2 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19007 | hp1 | a0002 | c0002 | t0003 | g0246 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0077 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0268 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0317 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19043 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19056 | hp1 | a0002 | c0003 | t0001 | g0031 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19057 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19062 | hp1 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19062 | hp2 | a0002 | c0002 | t0003 | g0279 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19070 | hp2 | a0002 | c0002 | t0003 | g0263 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19076 | hp2 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19077 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19078 | hp2 | a0002 | c0003 | t0001 | g0067 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19081 | hp1 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19082 | hp2 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19084 | hp1 | a0002 | c0003 | t0001 | g0003 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19084 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19085 | hp1 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19086 | hp2 | a0002 | c0002 | t0003 | g0273 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19088 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19090 | hp1 | a0001 | c0001 | t0016 | g0325 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA19240 | hp2 | a0003 | c0005 | t0006 | g0326 | AFR | YRI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ASW | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20129 | hp2 | a0005 | c0007 | t0009 | g0244 | AFR | ASW | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0089 | EUR | TSI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20752 | hp2 | a0002 | c0003 | t0001 | g0055 | EUR | TSI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20805 | hp1 | a0002 | c0003 | t0002 | g0049 | EUR | TSI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0147 | EUR | TSI | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | GIH | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | GIH | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG01123 | hp2 | a0001 | c0001 | t0005 | g0096 | AMR | CLM | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02109 | hp2 | a0002 | c0002 | t0008 | g0265 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02486 | hp1 | a0002 | c0002 | t0003 | g0247 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG02559 | hp2 | a0003 | c0005 | t0006 | g0028 | AFR | ACB | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03471 | hp1 | a0002 | c0002 | t0003 | g0010 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG03471 | hp2 | a0004 | c0006 | t0004 | g0319 | AFR | MSL | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | USA | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | USA | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18955 | hp1 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20300 | hp1 | a0002 | c0002 | t0010 | g0250 | AFR | USA | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | USA | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | LWK | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0003 | g0264 | REF | REF | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0181 | REF | REF | FOLH1_chr11_49140092_49213602 | FOLH1 | chr11 | 49140092 | 49213602 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:49164722
|
G | A | 2 | a0004a0005 | 7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
missense_variant | MODERATE | c.1423C>T | p.His475Tyr | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/19 | 1616/4110 | 1423/2253 | 475/750 | chr11 | 49164722 | ||
chr11:49192842
|
G | A | 1 | a0004 | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
missense_variant | MODERATE | c.464C>T | p.Ser155Leu | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/19 | 657/4110 | 464/2253 | 155/750 | chr11 | 49192842 | ||
chr11:49206068
|
A | G | 1 | a0002 | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
missense_variant&splice_region_variant | MODERATE | c.223T>C | p.Tyr75His | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/19 | 416/4110 | 223/2253 | 75/750 | chr11 | 49206068 | ||
chr11:49208393
|
TGAA | T | 1 | a0003 | 6 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
disruptive_inframe_deletion | MODERATE | c.14_16delTTC | p.Leu5del | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/19 | 209/4110 | 14/2253 | 5/750 | chr11 | 49208393 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:49146864
|
A | G | 1 | a0001c0009 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.2145T>C | p.Ile715Ile | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 2338/4110 | 2145/2253 | 715/750 | chr11 | 49146864 | ||
chr11:49153923
|
T | C | 1 | a0001c0010 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.1893A>G | p.Ser631Ser | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/19 | 2086/4110 | 1893/2253 | 631/750 | chr11 | 49153923 | ||
chr11:49174938
|
T | C | 5 | a0001c0004a0002c0002a0002c0003others(2): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
synonymous_variant | LOW | c.1059A>G | p.Thr353Thr | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/19 | 1252/4110 | 1059/2253 | 353/750 | chr11 | 49174938 | ||
chr11:49175864
|
A | G | 2 | a0001c0004a0002c0003 | 74 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(71): Show |
synonymous_variant | LOW | c.1014T>C | p.Ser338Ser | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/19 | 1207/4110 | 1014/2253 | 338/750 | chr11 | 49175864 | ||
chr11:49185763
|
A | G | 4 | a0002c0002a0002c0003a0002c0011others(1): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
synonymous_variant | LOW | c.732T>C | p.Asp244Asp | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/19 | 925/4110 | 732/2253 | 244/750 | chr11 | 49185763 | ||
chr11:49186746
|
A | G | 1 | a0001c0008 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.537T>C | p.Tyr179Tyr | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/19 | 730/4110 | 537/2253 | 179/750 | chr11 | 49186746 | ||
chr11:49200333
|
T | A | 5 | a0002c0002a0002c0003a0002c0011others(2): Show | 173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
synonymous_variant | LOW | c.333A>T | p.Ala111Ala | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/19 | 526/4110 | 333/2253 | 111/750 | chr11 | 49200333 | ||
chr11:49200339
|
C | T | 1 | a0002c0011 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.327G>A | p.Glu109Glu | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/19 | 520/4110 | 327/2253 | 109/750 | chr11 | 49200339 | ||
chr11:49206156
|
G | A | 1 | a0002c0011 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.135C>T | p.Ser45Ser | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/19 | 328/4110 | 135/2253 | 45/750 | chr11 | 49206156 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:49145177
|
C | T | 1 | a0002c0003t0013 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1579G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1579 | chr11 | 49145177 | |||||
chr11:49145178
|
A | G | 14 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(11): Show | 154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1578T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1578 | chr11 | 49145178 | |||||
chr11:49145304
|
C | G | 1 | a0005c0007t0009 | 2 | HG01346.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1452G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1452 | chr11 | 49145304 | |||||
chr11:49145386
|
T | C | 1 | a0002c0002t0010 | 2 | NA18522.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1370A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1370 | chr11 | 49145386 | |||||
chr11:49145600
|
G | A | 1 | a0001c0001t0014 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1156C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 1156 | chr11 | 49145600 | |||||
chr11:49145863
|
G | A | 2 | a0002c0002t0004a0004c0006t0004 | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 893 | chr11 | 49145863 | |||||
chr11:49146084
|
T | C | 2 | a0002c0002t0004a0004c0006t0004 | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*672A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 672 | chr11 | 49146084 | |||||
chr11:49146109
|
T | C | 1 | a0001c0001t0015 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*647A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 647 | chr11 | 49146109 | |||||
chr11:49146356
|
C | T | 1 | a0001c0001t0012 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*400G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 400 | chr11 | 49146356 | |||||
chr11:49146400
|
G | A | 1 | a0001c0001t0005 | 5 | HG00099.hp1 HG00140.hp2 HG01123.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*356C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 356 | chr11 | 49146400 | |||||
chr11:49146414
|
A | G | 1 | a0001c0001t0011 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 342 | chr11 | 49146414 | |||||
chr11:49146464
|
C | G | 1 | a0002c0002t0008 | 3 | HG02109.hp2 HG02698.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*292G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 292 | chr11 | 49146464 | |||||
chr11:49146626
|
T | C | 1 | a0001c0001t0007 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*130A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 130 | chr11 | 49146626 | |||||
chr11:49146748
|
G | A | 3 | a0002c0002t0003a0002c0002t0008a0002c0002t0010 | 71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*8C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 19/19 | 8 | chr11 | 49146748 | |||||
chr11:49208425
|
G | A | 1 | a0001c0001t0016 | 1 | NA19090.hp1 | 5_prime_UTR_variant | MODIFIER | c.-16C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/19 | 16 | chr11 | 49208425 | |||||
chr11:49208591
|
C | A | 1 | a0003c0005t0006 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-182G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/19 | 182 | chr11 | 49208591 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:49146960
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.2064-15C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49146960 | ||||||
chr11:49147060
|
T | C | 53 | a0002c0002t0003g0001a0002c0002t0003g0010a0002c0002t0003g0011others(50): Show | 71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2064-115A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147060 | ||||||
chr11:49147159
|
G | C | 6 | a0002c0002t0001g0307a0002c0002t0001g0308a0002c0002t0001g0309others(3): Show | 6 | HG02723.hp1 HG02922.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2064-214C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147159 | ||||||
chr11:49147241
|
A | G | 1 | a0001c0001t0002g0152 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2064-296T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147241 | ||||||
chr11:49147267
|
T | C | 5 | a0002c0003t0001g0051a0002c0003t0001g0068a0002c0003t0001g0069others(2): Show | 5 | HG01361.hp1 HG01952.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.2064-322A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147267 | ||||||
chr11:49147446
|
GT | G | 288 | a0001c0001t0001g0229a0001c0001t0002g0002a0001c0001t0002g0005others(285): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.2064-502delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147446 | ||||||
chr11:49147734
|
C | T | 2 | a0002c0002t0001g0025a0002c0002t0001g0316 | 3 | HG02896.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2064-789G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147734 | ||||||
chr11:49147755
|
C | A | 1 | a0005c0007t0009g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2064-810G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147755 | ||||||
chr11:49147931
|
GA | G | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2063+707delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49147931 | ||||||
chr11:49148234
|
A | G | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2063+405T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49148234 | ||||||
chr11:49148301
|
T | C | 68 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(65): Show | 73 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.2063+338A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 18/18 | chr11 | 49148301 | ||||||
chr11:49148782
|
T | C | 290 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(287): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1971-51A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49148782 | ||||||
chr11:49148979
|
G | A | 1 | a0002c0002t0003g0276 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1971-248C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49148979 | ||||||
chr11:49149038
|
A | G | 1 | a0002c0002t0001g0293 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1971-307T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149038 | ||||||
chr11:49149114
|
G | C | 1 | a0001c0001t0002g0189 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1971-383C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149114 | ||||||
chr11:49149116
|
T | G | 45 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0098others(42): Show | 49 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.1971-385A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149116 | ||||||
chr11:49149222
|
T | C | 91 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(88): Show | 96 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1971-491A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149222 | ||||||
chr11:49149423
|
G | T | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1971-692C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149423 | ||||||
chr11:49149538
|
G | A | 1 | a0002c0003t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1971-807C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149538 | ||||||
chr11:49149744
|
T | A | 322 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(319): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1971-1013A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149744 | ||||||
chr11:49149870
|
G | A | 4 | a0002c0002t0001g0245a0002c0002t0001g0301a0002c0002t0001g0302others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1971-1139C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149870 | ||||||
chr11:49149997
|
G | A | 1 | a0005c0007t0009g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1971-1266C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49149997 | ||||||
chr11:49150113
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1971-1382A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150113 | ||||||
chr11:49150138
|
T | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1971-1407A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150138 | ||||||
chr11:49150162
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1971-1431G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150162 | ||||||
chr11:49150169
|
T | C | 129 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(126): Show | 143 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1971-1438A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150169 | ||||||
chr11:49150203
|
T | C | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1971-1472A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150203 | ||||||
chr11:49150290
|
C | T | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1971-1559G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150290 | ||||||
chr11:49150397
|
T | C | 1 | a0001c0001t0005g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1971-1666A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150397 | ||||||
chr11:49150442
|
A | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1971-1711T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150442 | ||||||
chr11:49150463
|
C | G | 1 | a0002c0003t0001g0054 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1971-1732G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150463 | ||||||
chr11:49150519
|
T | C | 4 | a0001c0001t0007g0008a0003c0005t0006g0028a0003c0005t0006g0326others(1): Show | 7 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1971-1788A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150519 | ||||||
chr11:49150571
|
T | C | 1 | a0002c0002t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1971-1840A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150571 | ||||||
chr11:49150867
|
G | A | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1971-2136C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49150867 | ||||||
chr11:49151137
|
G | A | 8 | a0002c0002t0001g0307a0002c0002t0001g0308a0002c0002t0001g0309others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1971-2406C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151137 | ||||||
chr11:49151375
|
C | CAT | 322 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(319): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1970+2470_1970+247 others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151375 | ||||||
chr11:49151389
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1970+2457G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151389 | ||||||
chr11:49151390
|
G | A | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1970+2456C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151390 | ||||||
chr11:49151397
|
C | T | 1 | a0002c0003t0001g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1970+2449G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151397 | ||||||
chr11:49151407
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1970+2439G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151407 | ||||||
chr11:49151408
|
G | A | 38 | a0002c0003t0001g0013a0002c0003t0001g0031a0002c0003t0001g0035others(35): Show | 39 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1970+2438C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151408 | ||||||
chr11:49151414
|
G | GCA | 3 | a0002c0003t0001g0084a0002c0003t0001g0085a0002c0003t0001g0086 | 3 | HG00544.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1970+2430_1970+243 others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151414 | ||||||
chr11:49151427
|
C | CACAG | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+2418_1970+241 others(8): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151427 | ||||||
chr11:49151429
|
G | C | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+2417C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151429 | ||||||
chr11:49151429
|
GAC | G | 56 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(53): Show | 74 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1970+2415_1970+241 others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151429 | ||||||
chr11:49151601
|
C | CTAT | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1970+2242_1970+224 others(7): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151601 | ||||||
chr11:49151682
|
T | C | 135 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(132): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1970+2164A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151682 | ||||||
chr11:49151779
|
A | G | 287 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(284): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.1970+2067T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151779 | ||||||
chr11:49151804
|
T | G | 1 | a0002c0002t0003g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1970+2042A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151804 | ||||||
chr11:49151885
|
T | C | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+1961A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151885 | ||||||
chr11:49151956
|
C | T | 1 | a0002c0003t0001g0082 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1970+1890G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49151956 | ||||||
chr11:49152047
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1970+1799G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152047 | ||||||
chr11:49152048
|
A | G | 4 | a0002c0002t0003g0021a0002c0002t0003g0247a0002c0002t0003g0248others(1): Show | 5 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1970+1798T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152048 | ||||||
chr11:49152074
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1970+1772T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152074 | ||||||
chr11:49152327
|
T | G | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+1519A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152327 | ||||||
chr11:49152455
|
A | C | 130 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(127): Show | 146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1970+1391T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152455 | ||||||
chr11:49152589
|
G | T | 290 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(287): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.1970+1257C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152589 | ||||||
chr11:49152616
|
G | A | 1 | a0002c0002t0003g0298 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1970+1230C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152616 | ||||||
chr11:49152692
|
C | A | 1 | a0001c0001t0002g0125 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1970+1154G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152692 | ||||||
chr11:49152751
|
C | T | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1970+1095G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152751 | ||||||
chr11:49152792
|
T | C | 3 | a0002c0002t0003g0263a0002c0002t0003g0274a0002c0002t0003g0278 | 3 | NA18946.hp1 NA18953.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1970+1054A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152792 | ||||||
chr11:49152815
|
T | C | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1970+1031A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152815 | ||||||
chr11:49152886
|
T | C | 6 | a0001c0001t0007g0008a0003c0005t0002g0029a0003c0005t0002g0030others(3): Show | 9 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1970+960A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49152886 | ||||||
chr11:49153106
|
T | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1970+740A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153106 | ||||||
chr11:49153390
|
T | C | 287 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(284): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
intron_variant | MODIFIER | c.1970+456A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153390 | ||||||
chr11:49153600
|
G | C | 1 | a0001c0001t0002g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1970+246C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153600 | ||||||
chr11:49153691
|
T | C | 1 | a0002c0002t0003g0270 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1970+155A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153691 | ||||||
chr11:49153704
|
C | G | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1970+142G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 17/18 | chr11 | 49153704 | ||||||
chr11:49153999
|
A | G | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1889-72T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 16/18 | chr11 | 49153999 | ||||||
chr11:49154505
|
C | T | 141 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(138): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1624-13G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154505 | ||||||
chr11:49154506
|
A | G | 22 | a0002c0003t0001g0003a0002c0003t0001g0004a0002c0003t0001g0032others(19): Show | 26 | HG00597.hp1 HG00609.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1624-14T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154506 | ||||||
chr11:49154591
|
G | A | 1 | a0002c0003t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1624-99C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154591 | ||||||
chr11:49154626
|
A | G | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1624-134T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154626 | ||||||
chr11:49154675
|
A | G | 48 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(45): Show | 54 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1624-183T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154675 | ||||||
chr11:49154714
|
T | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-222A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154714 | ||||||
chr11:49154759
|
G | A | 2 | a0002c0003t0001g0031a0002c0003t0001g0037 | 2 | NA19056.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1624-267C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154759 | ||||||
chr11:49154806
|
A | T | 3 | a0001c0001t0002g0141a0001c0001t0002g0195a0001c0001t0002g0196 | 3 | HG00558.hp1 NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1624-314T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154806 | ||||||
chr11:49154933
|
A | G | 1 | a0001c0001t0002g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1624-441T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154933 | ||||||
chr11:49154952
|
A | G | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1624-460T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49154952 | ||||||
chr11:49155393
|
A | G | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1624-901T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155393 | ||||||
chr11:49155501
|
A | C | 1 | a0001c0001t0001g0239 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1624-1009T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155501 | ||||||
chr11:49155597
|
G | T | 1 | a0001c0001t0002g0134 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1624-1105C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155597 | ||||||
chr11:49155695
|
A | T | 92 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(89): Show | 97 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1623+1022T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155695 | ||||||
chr11:49155795
|
C | CAT | 44 | a0001c0001t0001g0122a0001c0001t0001g0221a0001c0001t0001g0225others(41): Show | 48 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1623+920_1623+921d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
C | CATAT | 43 | a0001c0001t0001g0020a0001c0001t0001g0219a0001c0001t0001g0220others(40): Show | 47 | HG00140.hp1 HG00558.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.1623+918_1623+921d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
C | CATATAT | 52 | a0001c0001t0001g0019a0001c0001t0001g0218a0001c0001t0001g0223others(49): Show | 62 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1623+916_1623+921d others(8): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
C | CATATATA others(1): Show |
45 | a0001c0001t0001g0009a0001c0001t0001g0222a0001c0001t0001g0241others(42): Show | 48 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.1623+914_1623+921d others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
C | CATATATA others(3): Show |
22 | a0001c0001t0001g0226a0001c0001t0002g0089a0001c0001t0002g0105others(19): Show | 22 | HG01168.hp1 HG01175.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1623+912_1623+921d others(12): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
C | CATATATA others(5): Show |
10 | a0001c0001t0002g0145a0001c0001t0002g0179a0001c0001t0002g0187others(7): Show | 10 | HG00597.hp1 HG01993.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.1623+910_1623+921d others(14): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
C | CATATATA others(7): Show |
3 | a0001c0001t0002g0144a0002c0003t0001g0072a0002c0003t0002g0049 | 3 | HG00280.hp2 HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1623+908_1623+921d others(16): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CAT | C | 4 | a0001c0001t0002g0175a0002c0002t0001g0308a0002c0002t0001g0311others(1): Show | 4 | HG00735.hp1 HG01346.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1623+920_1623+921d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CATAT | C | 6 | a0002c0002t0001g0300a0002c0002t0001g0309a0002c0002t0001g0310others(3): Show | 7 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1623+918_1623+921d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CATATATA others(1): Show |
C | 7 | a0001c0001t0002g0016a0001c0001t0002g0101a0001c0001t0002g0165others(4): Show | 10 | HG02109.hp1 HG02293.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1623+914_1623+921d others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0002g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1623+912_1623+921d others(12): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CATATATA others(5): Show |
C | 5 | a0001c0001t0002g0119a0002c0002t0004g0313a0004c0006t0004g0026others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623+910_1623+921d others(14): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CATATATA others(7): Show |
C | 3 | a0002c0002t0001g0305a0002c0002t0001g0306a0002c0011t0001g0312 | 3 | HG01109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1623+908_1623+921d others(16): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CATATATA others(9): Show |
C | 5 | a0002c0002t0003g0248a0002c0002t0003g0252a0002c0002t0003g0253others(2): Show | 5 | HG01243.hp1 HG02647.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+906_1623+921d others(18): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CATATATA others(11): Show |
C | 49 | a0001c0001t0001g0238a0002c0002t0002g0268a0002c0002t0003g0001others(46): Show | 67 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1623+904_1623+921d others(20): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155795
|
CATATATA others(13): Show |
C | 2 | a0001c0001t0002g0183a0002c0002t0003g0272 | 2 | HG00609.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1623+902_1623+921d others(22): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155795 | ||||||
chr11:49155835
|
T | TATATATA others(3): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0322a0002c0002t0001g0307 | 4 | HG02559.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+881_1623+882i others(12): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155835 | ||||||
chr11:49155835
|
T | TATATATA others(5): Show |
1 | a0002c0002t0001g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1623+881_1623+882i others(14): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155835 | ||||||
chr11:49155842
|
C | T | 3 | a0001c0001t0002g0095a0001c0001t0002g0106a0001c0001t0002g0107 | 3 | HG02280.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1623+875G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155842 | ||||||
chr11:49155967
|
C | A | 27 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(24): Show | 31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1623+750G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49155967 | ||||||
chr11:49156124
|
T | C | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1623+593A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156124 | ||||||
chr11:49156256
|
T | C | 13 | a0001c0001t0007g0008a0002c0002t0004g0313a0003c0005t0002g0029others(10): Show | 17 | HG01109.hp1 HG01346.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1623+461A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156256 | ||||||
chr11:49156311
|
A | G | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1623+406T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156311 | ||||||
chr11:49156367
|
T | C | 1 | a0001c0001t0005g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1623+350A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156367 | ||||||
chr11:49156545
|
A | C | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1623+172T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156545 | ||||||
chr11:49156551
|
T | C | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1623+166A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156551 | ||||||
chr11:49156588
|
T | C | 16 | a0001c0001t0002g0017a0001c0001t0002g0115a0001c0001t0002g0125others(13): Show | 17 | HG00544.hp1 HG02300.hp1 NA18747.hp2 others(14): Show |
intron_variant | MODIFIER | c.1623+129A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156588 | ||||||
chr11:49156702
|
T | C | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1623+15A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 15/18 | chr11 | 49156702 | ||||||
chr11:49156921
|
A | G | 1 | a0002c0002t0003g0282 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1533-114T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49156921 | ||||||
chr11:49156929
|
A | G | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-122T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49156929 | ||||||
chr11:49157105
|
C | T | 2 | a0002c0002t0003g0256a0002c0002t0003g0257 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1533-298G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157105 | ||||||
chr11:49157352
|
C | T | 1 | a0001c0001t0002g0143 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1533-545G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157352 | ||||||
chr11:49157465
|
A | G | 27 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(24): Show | 31 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1532+487T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157465 | ||||||
chr11:49157539
|
T | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1532+413A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157539 | ||||||
chr11:49157596
|
C | G | 322 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(319): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1532+356G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157596 | ||||||
chr11:49157737
|
C | T | 92 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(89): Show | 97 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1532+215G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157737 | ||||||
chr11:49157838
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1532+114C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157838 | ||||||
chr11:49157858
|
C | A | 1 | a0001c0001t0002g0151 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1532+94G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 14/18 | chr11 | 49157858 | ||||||
chr11:49158044
|
C | T | 1 | a0002c0002t0010g0249 | 1 | NA18522.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1441-1G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158044 | ||||||
chr11:49158177
|
C | T | 3 | a0002c0003t0001g0084a0002c0003t0001g0085a0002c0003t0001g0086 | 3 | HG00544.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1441-134G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158177 | ||||||
chr11:49158256
|
T | C | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1441-213A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158256 | ||||||
chr11:49158288
|
C | G | 1 | a0001c0001t0002g0182 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1441-245G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158288 | ||||||
chr11:49158436
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1441-393C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158436 | ||||||
chr11:49158556
|
G | T | 128 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(125): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1441-513C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158556 | ||||||
chr11:49158633
|
T | C | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-590A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158633 | ||||||
chr11:49158717
|
T | G | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1441-674A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158717 | ||||||
chr11:49158731
|
G | A | 1 | a0002c0003t0001g0037 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1441-688C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158731 | ||||||
chr11:49158908
|
G | T | 7 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(4): Show | 8 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1441-865C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158908 | ||||||
chr11:49158975
|
T | C | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-932A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49158975 | ||||||
chr11:49159056
|
T | C | 134 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(131): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1441-1013A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159056 | ||||||
chr11:49159284
|
A | G | 1 | a0002c0002t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1441-1241T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159284 | ||||||
chr11:49159356
|
T | C | 5 | a0002c0002t0004g0313a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1441-1313A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159356 | ||||||
chr11:49159875
|
G | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-1832C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159875 | ||||||
chr11:49159906
|
C | CT | 7 | a0001c0001t0002g0130a0002c0002t0003g0274a0002c0002t0003g0297others(4): Show | 8 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1441-1864dupA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159906 | ||||||
chr11:49159906
|
CT | C | 29 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0016others(26): Show | 34 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.1441-1864delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159906 | ||||||
chr11:49159960
|
T | C | 7 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(4): Show | 8 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1441-1917A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49159960 | ||||||
chr11:49160014
|
G | A | 1 | a0002c0002t0001g0302 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1441-1971C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160014 | ||||||
chr11:49160037
|
C | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1441-1994G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160037 | ||||||
chr11:49160040
|
G | A | 1 | a0001c0001t0002g0107 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1441-1997C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160040 | ||||||
chr11:49160374
|
G | T | 1 | a0001c0001t0002g0129 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1441-2331C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160374 | ||||||
chr11:49160444
|
T | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-2401A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160444 | ||||||
chr11:49160503
|
C | T | 1 | a0002c0002t0003g0254 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1441-2460G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160503 | ||||||
chr11:49160504
|
G | A | 5 | a0002c0002t0003g0011a0002c0002t0003g0264a0002c0002t0003g0276others(2): Show | 7 | HG00733.hp1 HG01081.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1441-2461C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160504 | ||||||
chr11:49160593
|
C | T | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-2550G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160593 | ||||||
chr11:49160635
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1441-2592C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160635 | ||||||
chr11:49160741
|
C | A | 1 | a0002c0003t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1441-2698G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160741 | ||||||
chr11:49160742
|
A | G | 1 | a0002c0003t0001g0072 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1441-2699T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160742 | ||||||
chr11:49160873
|
T | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1441-2830A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160873 | ||||||
chr11:49160911
|
G | A | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1441-2868C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160911 | ||||||
chr11:49160923
|
A | C | 2 | a0002c0002t0003g0256a0002c0002t0003g0257 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1441-2880T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160923 | ||||||
chr11:49160982
|
G | A | 1 | a0002c0003t0001g0070 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1441-2939C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160982 | ||||||
chr11:49160995
|
A | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1441-2952T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160995 | ||||||
chr11:49160996
|
C | T | 1 | a0002c0002t0003g0024 | 2 | HG01346.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1441-2953G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49160996 | ||||||
chr11:49161008
|
C | A | 1 | a0001c0001t0012g0184 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1441-2965G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161008 | ||||||
chr11:49161096
|
C | T | 3 | a0002c0002t0001g0314a0002c0002t0001g0315a0002c0002t0004g0313 | 3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1441-3053G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161096 | ||||||
chr11:49161392
|
T | C | 2 | a0003c0005t0002g0029a0003c0005t0002g0030 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1440+3313A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161392 | ||||||
chr11:49161397
|
T | G | 1 | a0001c0001t0002g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1440+3308A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161397 | ||||||
chr11:49161402
|
T | A | 1 | a0001c0001t0002g0136 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1440+3303A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161402 | ||||||
chr11:49161515
|
T | C | 1 | a0002c0003t0001g0038 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1440+3190A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161515 | ||||||
chr11:49161664
|
T | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1440+3041A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161664 | ||||||
chr11:49161741
|
GT | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+2963delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161741 | ||||||
chr11:49161852
|
T | G | 1 | a0002c0002t0004g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1440+2853A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161852 | ||||||
chr11:49161854
|
A | G | 128 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(125): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1440+2851T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161854 | ||||||
chr11:49161951
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1440+2754G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49161951 | ||||||
chr11:49162014
|
C | T | 1 | a0001c0001t0011g0142 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1440+2691G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162014 | ||||||
chr11:49162189
|
AG | A | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1440+2515delC | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162189 | ||||||
chr11:49162535
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1440+2170G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162535 | ||||||
chr11:49162617
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1440+2088C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162617 | ||||||
chr11:49162619
|
T | C | 5 | a0002c0002t0002g0268a0002c0002t0003g0022a0002c0002t0003g0261others(2): Show | 6 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1440+2086A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162619 | ||||||
chr11:49162753
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1440+1952C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162753 | ||||||
chr11:49162810
|
G | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1440+1895C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162810 | ||||||
chr11:49162837
|
G | A | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1440+1868C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162837 | ||||||
chr11:49162854
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1440+1851G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162854 | ||||||
chr11:49162959
|
C | T | 1 | a0002c0002t0003g0304 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1440+1746G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49162959 | ||||||
chr11:49163036
|
T | C | 1 | a0002c0002t0003g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1440+1669A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163036 | ||||||
chr11:49163649
|
A | G | 139 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(136): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1440+1056T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163649 | ||||||
chr11:49163697
|
G | A | 1 | a0002c0002t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1440+1008C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163697 | ||||||
chr11:49163760
|
T | C | 6 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(3): Show | 7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+945A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163760 | ||||||
chr11:49163855
|
C | T | 7 | a0001c0001t0002g0014a0001c0001t0002g0137a0001c0001t0002g0138others(4): Show | 8 | HG00438.hp1 NA18960.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1440+850G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163855 | ||||||
chr11:49163862
|
G | A | 54 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(51): Show | 58 | HG00597.hp1 HG00609.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.1440+843C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163862 | ||||||
chr11:49163887
|
T | C | 2 | a0001c0001t0002g0094a0001c0001t0002g0162 | 2 | HG01358.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1440+818A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163887 | ||||||
chr11:49163929
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1440+776C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163929 | ||||||
chr11:49163972
|
C | T | 128 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(125): Show | 142 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1440+733G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49163972 | ||||||
chr11:49164022
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1440+683A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164022 | ||||||
chr11:49164054
|
T | C | 4 | a0002c0002t0003g0001a0002c0002t0003g0273a0002c0002t0003g0277others(1): Show | 12 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(9): Show |
intron_variant | MODIFIER | c.1440+651A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164054 | ||||||
chr11:49164370
|
G | A | 5 | a0001c0001t0002g0017a0001c0001t0002g0156a0001c0001t0002g0172others(2): Show | 6 | NA18939.hp2 NA18942.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1440+335C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164370 | ||||||
chr11:49164405
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1440+300T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164405 | ||||||
chr11:49164449
|
C | T | 1 | a0002c0002t0010g0249 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1440+256G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164449 | ||||||
chr11:49164639
|
C | CATA | 6 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(3): Show | 7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1440+63_1440+65dup others(3): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 13/18 | chr11 | 49164639 | ||||||
chr11:49164911
|
C | G | 1 | a0002c0002t0001g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1373-139G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49164911 | ||||||
chr11:49164918
|
T | G | 2 | a0001c0001t0002g0140a0001c0001t0002g0164 | 2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1373-146A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49164918 | ||||||
chr11:49165038
|
G | T | 6 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(3): Show | 7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-266C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165038 | ||||||
chr11:49165101
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1373-329G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165101 | ||||||
chr11:49165129
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1373-357G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165129 | ||||||
chr11:49165163
|
C | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1373-391G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165163 | ||||||
chr11:49165204
|
G | T | 1 | a0001c0001t0002g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1373-432C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165204 | ||||||
chr11:49165225
|
A | C | 1 | a0002c0011t0001g0312 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1373-453T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165225 | ||||||
chr11:49165346
|
T | G | 4 | a0002c0002t0001g0245a0002c0002t0001g0301a0002c0002t0001g0302others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-574A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165346 | ||||||
chr11:49165443
|
G | A | 1 | a0002c0003t0001g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1373-671C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165443 | ||||||
chr11:49165619
|
T | C | 1 | a0001c0010t0002g0210 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1373-847A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165619 | ||||||
chr11:49165627
|
A | G | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1373-855T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165627 | ||||||
chr11:49165732
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1373-960C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165732 | ||||||
chr11:49165810
|
G | T | 1 | a0005c0007t0009g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1373-1038C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49165810 | ||||||
chr11:49166113
|
A | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0237 | 3 | HG03139.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1373-1341T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166113 | ||||||
chr11:49166155
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1373-1383G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166155 | ||||||
chr11:49166292
|
G | A | 6 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(3): Show | 7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-1520C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166292 | ||||||
chr11:49166495
|
G | C | 8 | a0002c0002t0001g0289a0002c0002t0001g0290a0002c0002t0001g0291others(5): Show | 8 | HG02486.hp2 HG02622.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1373-1723C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166495 | ||||||
chr11:49166629
|
G | T | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1373-1857C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166629 | ||||||
chr11:49166634
|
G | A | 6 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(3): Show | 7 | HG01346.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1373-1862C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166634 | ||||||
chr11:49166679
|
C | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1373-1907G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166679 | ||||||
chr11:49166701
|
A | G | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1373-1929T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166701 | ||||||
chr11:49166745
|
T | C | 141 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(138): Show | 159 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1373-1973A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166745 | ||||||
chr11:49166745
|
T | G | 1 | a0001c0001t0002g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1373-1973A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166745 | ||||||
chr11:49166844
|
G | C | 1 | a0001c0001t0002g0157 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1373-2072C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166844 | ||||||
chr11:49166953
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1373-2181C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166953 | ||||||
chr11:49166975
|
G | T | 7 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(4): Show | 7 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1373-2203C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49166975 | ||||||
chr11:49167046
|
C | A | 15 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(12): Show | 20 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1372+2149G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167046 | ||||||
chr11:49167046
|
CAAA | C | 130 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(127): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1372+2146_1372+214 others(7): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167046 | ||||||
chr11:49167049
|
A | C | 10 | a0001c0001t0007g0008a0003c0005t0002g0029a0003c0005t0002g0030others(7): Show | 14 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1372+2146T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167049 | ||||||
chr11:49167186
|
A | G | 8 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02630.hp1 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1372+2009T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167186 | ||||||
chr11:49167243
|
C | G | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1372+1952G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167243 | ||||||
chr11:49167273
|
T | C | 136 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(133): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1372+1922A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167273 | ||||||
chr11:49167343
|
A | G | 1 | a0002c0003t0013g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1372+1852T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167343 | ||||||
chr11:49167437
|
T | C | 9 | a0001c0001t0002g0105a0001c0001t0002g0187a0001c0001t0002g0188others(6): Show | 9 | NA18948.hp1 NA18953.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1372+1758A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167437 | ||||||
chr11:49167471
|
C | T | 150 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(147): Show | 174 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1372+1724G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167471 | ||||||
chr11:49167539
|
G | A | 150 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(147): Show | 174 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1372+1656C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167539 | ||||||
chr11:49167589
|
T | C | 150 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(147): Show | 174 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1372+1606A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167589 | ||||||
chr11:49167615
|
G | A | 136 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(133): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1372+1580C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167615 | ||||||
chr11:49167683
|
G | A | 93 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(90): Show | 98 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1372+1512C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167683 | ||||||
chr11:49167685
|
T | C | 1 | a0001c0001t0002g0099 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1372+1510A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167685 | ||||||
chr11:49167719
|
T | C | 4 | a0002c0002t0001g0245a0002c0002t0001g0301a0002c0002t0001g0302others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+1476A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167719 | ||||||
chr11:49167865
|
A | C | 189 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(186): Show | 219 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1372+1330T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167865 | ||||||
chr11:49167903
|
A | G | 1 | a0002c0002t0003g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1372+1292T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167903 | ||||||
chr11:49167923
|
C | A | 4 | a0001c0001t0002g0163a0002c0002t0001g0025a0002c0002t0001g0300others(1): Show | 5 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1372+1272G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167923 | ||||||
chr11:49167924
|
C | CAGAAAA | 321 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(318): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.1372+1265_1372+127 others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167924 | ||||||
chr11:49167958
|
G | A | 1 | a0002c0002t0003g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1372+1237C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49167958 | ||||||
chr11:49168000
|
C | G | 152 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(149): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1372+1195G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168000 | ||||||
chr11:49168044
|
C | CT | 37 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(34): Show | 42 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1372+1150dupA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168044 | ||||||
chr11:49168044
|
CT | C | 141 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(138): Show | 169 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.1372+1150delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168044 | ||||||
chr11:49168044
|
CTT | C | 16 | a0001c0004t0001g0111a0002c0002t0001g0289a0002c0002t0001g0290others(13): Show | 16 | HG01109.hp2 HG01346.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1372+1149_1372+115 others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168044 | ||||||
chr11:49168055
|
T | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1372+1140A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168055 | ||||||
chr11:49168059
|
TG | T | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1372+1135delC | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168059 | ||||||
chr11:49168074
|
A | C | 2 | a0001c0001t0002g0128a0001c0001t0002g0154 | 2 | NA18943.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1372+1121T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168074 | ||||||
chr11:49168090
|
G | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1105C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168090 | ||||||
chr11:49168092
|
C | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1103G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168092 | ||||||
chr11:49168093
|
G | C | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1102C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168093 | ||||||
chr11:49168095
|
TAGGAATC others(62): Show |
T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1031_1372+109 others(73): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168095 | ||||||
chr11:49168166
|
A | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1029T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168166 | ||||||
chr11:49168167
|
C | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1028G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168167 | ||||||
chr11:49168173
|
A | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1022T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168173 | ||||||
chr11:49168177
|
C | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+1018G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168177 | ||||||
chr11:49168182
|
TAATGACA others(149): Show |
T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+857_1372+1012 others(3): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168182 | ||||||
chr11:49168220
|
T | C | 1 | a0002c0003t0001g0066 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1372+975A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168220 | ||||||
chr11:49168231
|
C | T | 1 | a0002c0002t0003g0280 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1372+964G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168231 | ||||||
chr11:49168279
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1372+916A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168279 | ||||||
chr11:49168379
|
T | C | 4 | a0002c0002t0001g0245a0002c0002t0001g0301a0002c0002t0001g0302others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1372+816A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168379 | ||||||
chr11:49168479
|
C | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+716G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168479 | ||||||
chr11:49168600
|
A | G | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1372+595T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168600 | ||||||
chr11:49168691
|
G | A | 2 | a0001c0001t0001g0226a0001c0001t0001g0229 | 2 | NA18991.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1372+504C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168691 | ||||||
chr11:49168718
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1372+477C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168718 | ||||||
chr11:49168740
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1372+455G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168740 | ||||||
chr11:49168924
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1372+271A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168924 | ||||||
chr11:49168942
|
A | G | 1 | a0002c0002t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1372+253T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49168942 | ||||||
chr11:49169108
|
A | G | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+87T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 12/18 | chr11 | 49169108 | ||||||
chr11:49169308
|
T | A | 1 | a0001c0001t0002g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1309-50A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169308 | ||||||
chr11:49169309
|
C | T | 1 | a0001c0001t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1309-51G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169309 | ||||||
chr11:49169398
|
C | G | 1 | a0002c0003t0001g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1309-140G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169398 | ||||||
chr11:49169439
|
C | G | 292 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(289): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1309-181G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169439 | ||||||
chr11:49169611
|
C | T | 130 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(127): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1309-353G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169611 | ||||||
chr11:49169716
|
A | C | 1 | a0001c0001t0002g0137 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1309-458T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169716 | ||||||
chr11:49169816
|
G | A | 1 | a0002c0002t0003g0287 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1309-558C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169816 | ||||||
chr11:49169958
|
G | T | 2 | a0002c0002t0001g0307a0002c0002t0001g0317 | 2 | HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1309-700C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49169958 | ||||||
chr11:49170066
|
GGTTT | G | 152 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(149): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1309-812_1309-809d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170066 | ||||||
chr11:49170073
|
C | A | 1 | a0002c0002t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1309-815G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170073 | ||||||
chr11:49170182
|
T | G | 1 | a0002c0002t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1309-924A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170182 | ||||||
chr11:49170332
|
C | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308+863G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170332 | ||||||
chr11:49170348
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1308+847G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170348 | ||||||
chr11:49170359
|
A | G | 1 | a0002c0002t0003g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1308+836T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170359 | ||||||
chr11:49170431
|
A | G | 1 | a0001c0001t0002g0214 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1308+764T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170431 | ||||||
chr11:49170440
|
C | A | 1 | a0002c0002t0003g0259 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1308+755G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170440 | ||||||
chr11:49170476
|
G | A | 1 | a0002c0002t0003g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1308+719C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170476 | ||||||
chr11:49170540
|
G | A | 152 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(149): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.1308+655C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170540 | ||||||
chr11:49170672
|
G | A | 131 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(128): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1308+523C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170672 | ||||||
chr11:49170750
|
A | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+445T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170750 | ||||||
chr11:49170799
|
G | C | 150 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(147): Show | 174 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1308+396C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170799 | ||||||
chr11:49170974
|
T | C | 1 | a0002c0002t0008g0265 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1308+221A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170974 | ||||||
chr11:49170985
|
T | C | 1 | a0002c0003t0001g0013 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1308+210A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170985 | ||||||
chr11:49170999
|
T | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+196A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49170999 | ||||||
chr11:49171055
|
G | T | 1 | a0002c0002t0001g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1308+140C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49171055 | ||||||
chr11:49171075
|
T | G | 1 | a0003c0005t0002g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1308+120A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49171075 | ||||||
chr11:49171115
|
C | T | 131 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(128): Show | 147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1308+80G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49171115 | ||||||
chr11:49171138
|
T | C | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1308+57A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 11/18 | chr11 | 49171138 | ||||||
chr11:49171353
|
G | GA | 6 | a0001c0004t0001g0112a0002c0002t0001g0289a0002c0002t0001g0311others(3): Show | 6 | HG00544.hp2 HG01346.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1226-77dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49171353 | ||||||
chr11:49171353
|
GA | G | 152 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(149): Show | 172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1226-77delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49171353 | ||||||
chr11:49171440
|
T | C | 1 | a0002c0002t0003g0271 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1226-163A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49171440 | ||||||
chr11:49171535
|
T | A | 1 | a0002c0002t0003g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1226-258A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49171535 | ||||||
chr11:49172150
|
T | C | 7 | a0001c0001t0002g0014a0001c0001t0002g0137a0001c0001t0002g0138others(4): Show | 8 | HG00438.hp1 NA18960.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.1226-873A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172150 | ||||||
chr11:49172321
|
T | C | 2 | a0001c0001t0002g0116a0001c0001t0002g0200 | 2 | HG01175.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1225+1036A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172321 | ||||||
chr11:49172395
|
CA | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225+961delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172395 | ||||||
chr11:49172638
|
G | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+719C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172638 | ||||||
chr11:49172719
|
C | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225+638G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172719 | ||||||
chr11:49172744
|
T | A | 35 | a0001c0001t0002g0002a0001c0001t0002g0014a0001c0001t0002g0015others(32): Show | 41 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1225+613A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172744 | ||||||
chr11:49172813
|
A | G | 1 | a0002c0002t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1225+544T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172813 | ||||||
chr11:49172827
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1225+530C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172827 | ||||||
chr11:49172860
|
G | A | 1 | a0001c0001t0005g0097 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1225+497C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172860 | ||||||
chr11:49172918
|
G | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+439C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172918 | ||||||
chr11:49172933
|
G | A | 3 | a0001c0001t0002g0018a0001c0001t0002g0174a0001c0001t0002g0175 | 4 | HG00735.hp1 HG01099.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.1225+424C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172933 | ||||||
chr11:49172997
|
C | T | 1 | a0001c0001t0002g0165 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1225+360G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49172997 | ||||||
chr11:49173005
|
C | T | 1 | a0001c0001t0002g0188 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1225+352G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173005 | ||||||
chr11:49173082
|
A | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1225+275T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173082 | ||||||
chr11:49173338
|
T | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1225+19A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173338 | ||||||
chr11:49173342
|
G | A | 150 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(147): Show | 174 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1225+15C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173342 | ||||||
chr11:49173345
|
T | C | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1225+12A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 10/18 | chr11 | 49173345 | ||||||
chr11:49173538
|
T | C | 292 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(289): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1106-62A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173538 | ||||||
chr11:49173575
|
C | CA | 134 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(131): Show | 151 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1106-100dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173575 | ||||||
chr11:49173576
|
AG | A | 144 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.1106-101delC | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173576 | ||||||
chr11:49173577
|
G | A | 146 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(143): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.1106-101C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173577 | ||||||
chr11:49173620
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1106-144C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173620 | ||||||
chr11:49173648
|
T | G | 2 | a0001c0001t0002g0127a0001c0001t0002g0215 | 2 | NA18952.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1106-172A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173648 | ||||||
chr11:49173666
|
A | C | 1 | a0002c0003t0001g0079 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1106-190T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173666 | ||||||
chr11:49173716
|
C | T | 6 | a0001c0001t0002g0187a0001c0001t0002g0188a0001c0001t0002g0189others(3): Show | 6 | NA18948.hp1 NA18953.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.1106-240G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173716 | ||||||
chr11:49173779
|
T | TCC | 322 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(319): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1106-304_1106-303i others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173779 | ||||||
chr11:49173885
|
C | G | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1106-409G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173885 | ||||||
chr11:49173991
|
G | A | 130 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(127): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1106-515C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49173991 | ||||||
chr11:49174204
|
T | A | 136 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(133): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1105+688A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174204 | ||||||
chr11:49174248
|
C | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+644G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174248 | ||||||
chr11:49174250
|
G | C | 93 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(90): Show | 98 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1105+642C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174250 | ||||||
chr11:49174369
|
T | C | 150 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(147): Show | 174 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.1105+523A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174369 | ||||||
chr11:49174426
|
T | C | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1105+466A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174426 | ||||||
chr11:49174576
|
A | T | 136 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(133): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1105+316T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174576 | ||||||
chr11:49174603
|
C | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1105+289G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174603 | ||||||
chr11:49174685
|
AC | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1105+206delG | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174685 | ||||||
chr11:49174780
|
C | CGTTT | 5 | a0002c0003t0001g0035a0004c0006t0004g0026a0004c0006t0004g0318others(2): Show | 6 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1105+108_1105+111d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174780 | ||||||
chr11:49174780
|
C | T | 136 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(133): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1105+112G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174780 | ||||||
chr11:49174781
|
G | C | 129 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(126): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1105+111C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 9/18 | chr11 | 49174781 | ||||||
chr11:49175003
|
TA | T | 6 | a0001c0001t0002g0100a0002c0002t0003g0273a0004c0006t0004g0026others(3): Show | 7 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1020-27delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175003 | ||||||
chr11:49175040
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1020-63C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175040 | ||||||
chr11:49175100
|
C | T | 292 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(289): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1020-123G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175100 | ||||||
chr11:49175233
|
G | A | 93 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(90): Show | 98 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1020-256C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175233 | ||||||
chr11:49175334
|
CT | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1020-358delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175334 | ||||||
chr11:49175353
|
C | T | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1020-376G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175353 | ||||||
chr11:49175395
|
T | C | 91 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0005others(88): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1020-418A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175395 | ||||||
chr11:49175819
|
C | T | 2 | a0001c0001t0002g0128a0001c0001t0002g0154 | 2 | NA18943.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1019+40G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 8/18 | chr11 | 49175819 | ||||||
chr11:49175996
|
C | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.921-39G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49175996 | ||||||
chr11:49176225
|
A | T | 1 | a0002c0003t0001g0077 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.921-268T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176225 | ||||||
chr11:49176528
|
T | C | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.921-571A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176528 | ||||||
chr11:49176807
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.921-850C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176807 | ||||||
chr11:49176820
|
C | CTG | 152 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(149): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.921-864_921-863ins others(2): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176820 | ||||||
chr11:49176824
|
A | AAT | 152 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(149): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.921-868_921-867ins others(2): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176824 | ||||||
chr11:49176825
|
C | G | 152 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(149): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.921-868G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176825 | ||||||
chr11:49176912
|
G | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-955C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176912 | ||||||
chr11:49176947
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.921-990G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49176947 | ||||||
chr11:49177049
|
C | G | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.921-1092G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177049 | ||||||
chr11:49177055
|
C | T | 1 | a0002c0003t0001g0051 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.921-1098G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177055 | ||||||
chr11:49177177
|
C | T | 6 | a0002c0003t0001g0004a0002c0003t0001g0077a0002c0003t0001g0078others(3): Show | 8 | NA18944.hp1 NA18945.hp1 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.921-1220G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177177 | ||||||
chr11:49177247
|
T | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.921-1290A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177247 | ||||||
chr11:49177372
|
C | T | 152 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(149): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.921-1415G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177372 | ||||||
chr11:49177428
|
T | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-1471A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177428 | ||||||
chr11:49177622
|
C | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-1665G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177622 | ||||||
chr11:49177721
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.921-1764C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177721 | ||||||
chr11:49177730
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.921-1773G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177730 | ||||||
chr11:49177785
|
T | TA | 145 | a0001c0001t0001g0027a0001c0001t0001g0122a0001c0001t0001g0123others(142): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.921-1829dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177785 | ||||||
chr11:49177785
|
T | TAA | 7 | a0001c0001t0002g0098a0001c0001t0002g0103a0001c0001t0002g0154others(4): Show | 7 | HG02523.hp1 HG04115.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.921-1830_921-1829d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177785 | ||||||
chr11:49177785
|
TA | T | 10 | a0001c0001t0001g0221a0001c0001t0016g0325a0002c0002t0001g0308others(7): Show | 10 | HG00609.hp2 HG01346.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.921-1829delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177785 | ||||||
chr11:49177894
|
T | C | 4 | a0002c0002t0001g0245a0002c0002t0001g0301a0002c0002t0001g0302others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.921-1937A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177894 | ||||||
chr11:49177895
|
A | G | 1 | a0001c0001t0002g0201 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.921-1938T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177895 | ||||||
chr11:49177963
|
CA | C | 279 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(276): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.921-2007delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49177963 | ||||||
chr11:49178036
|
G | C | 325 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(322): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.921-2079C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178036 | ||||||
chr11:49178083
|
C | T | 1 | a0002c0002t0001g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.921-2126G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178083 | ||||||
chr11:49178111
|
G | T | 156 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(153): Show | 181 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.921-2154C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178111 | ||||||
chr11:49178196
|
A | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-2239T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178196 | ||||||
chr11:49178231
|
T | C | 1 | a0001c0001t0002g0203 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.921-2274A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178231 | ||||||
chr11:49178497
|
G | A | 322 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(319): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.921-2540C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178497 | ||||||
chr11:49178660
|
C | A | 1 | a0001c0004t0001g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.921-2703G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178660 | ||||||
chr11:49178775
|
G | A | 150 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(147): Show | 174 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.921-2818C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178775 | ||||||
chr11:49178820
|
C | G | 1 | a0001c0001t0002g0119 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.921-2863G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178820 | ||||||
chr11:49178840
|
T | G | 1 | a0002c0003t0001g0043 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.921-2883A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49178840 | ||||||
chr11:49179065
|
A | G | 6 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | NA18951.hp1 NA18964.hp1 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.921-3108T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179065 | ||||||
chr11:49179269
|
G | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-3312C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179269 | ||||||
chr11:49179329
|
C | T | 322 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(319): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.921-3372G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179329 | ||||||
chr11:49179398
|
T | G | 1 | a0002c0002t0001g0296 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.921-3441A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179398 | ||||||
chr11:49179517
|
G | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-3560C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179517 | ||||||
chr11:49179594
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.920+3555A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179594 | ||||||
chr11:49179626
|
T | C | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+3523A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179626 | ||||||
chr11:49179759
|
T | C | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.920+3390A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179759 | ||||||
chr11:49179810
|
C | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+3339G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179810 | ||||||
chr11:49179819
|
C | T | 152 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(149): Show | 176 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.920+3330G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179819 | ||||||
chr11:49179882
|
T | C | 2 | a0002c0002t0001g0025a0002c0002t0001g0316 | 3 | HG02896.hp2 HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.920+3267A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179882 | ||||||
chr11:49179914
|
A | T | 2 | a0001c0001t0002g0014a0001c0001t0002g0203 | 3 | NA18960.hp2 NA18978.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.920+3235T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49179914 | ||||||
chr11:49180061
|
C | T | 136 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(133): Show | 153 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.920+3088G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180061 | ||||||
chr11:49180062
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+3087C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180062 | ||||||
chr11:49180088
|
T | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+3061A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180088 | ||||||
chr11:49180116
|
C | G | 156 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(153): Show | 181 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.920+3033G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180116 | ||||||
chr11:49180128
|
C | T | 150 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(147): Show | 174 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.920+3021G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180128 | ||||||
chr11:49180142
|
A | ACTCT | 5 | a0003c0005t0002g0029a0003c0005t0002g0030a0003c0005t0006g0028others(2): Show | 6 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.920+3003_920+3006d others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180142 | ||||||
chr11:49180264
|
C | A | 292 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(289): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.920+2885G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180264 | ||||||
chr11:49180289
|
C | T | 5 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(2): Show | 5 | HG00544.hp1 HG02300.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+2860G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180289 | ||||||
chr11:49180352
|
A | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+2797T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180352 | ||||||
chr11:49180491
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.920+2658G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180491 | ||||||
chr11:49180503
|
A | G | 1 | a0001c0001t0002g0157 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.920+2646T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180503 | ||||||
chr11:49180611
|
T | C | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.920+2538A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180611 | ||||||
chr11:49180635
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+2514C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180635 | ||||||
chr11:49180642
|
A | T | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.920+2507T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180642 | ||||||
chr11:49180835
|
A | G | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+2314T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180835 | ||||||
chr11:49180874
|
C | T | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.920+2275G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180874 | ||||||
chr11:49180889
|
T | C | 1 | a0002c0002t0003g0261 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.920+2260A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49180889 | ||||||
chr11:49181017
|
G | A | 2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.920+2132C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181017 | ||||||
chr11:49181107
|
A | AT | 15 | a0001c0001t0001g0229a0001c0001t0001g0232a0002c0002t0001g0245others(12): Show | 15 | HG02145.hp1 HG02300.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.920+2041dupA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181107 | ||||||
chr11:49181107
|
AT | A | 140 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(137): Show | 157 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.920+2041delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181107 | ||||||
chr11:49181139
|
A | T | 1 | a0001c0001t0002g0124 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.920+2010T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181139 | ||||||
chr11:49181203
|
G | T | 1 | a0002c0003t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.920+1946C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181203 | ||||||
chr11:49181271
|
C | A | 1 | a0002c0002t0003g0252 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.920+1878G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181271 | ||||||
chr11:49181333
|
A | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+1816T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181333 | ||||||
chr11:49181448
|
A | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+1701T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181448 | ||||||
chr11:49181534
|
T | C | 3 | a0004c0006t0004g0318a0004c0006t0004g0319a0004c0006t0004g0320 | 3 | HG02615.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.920+1615A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181534 | ||||||
chr11:49181762
|
A | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+1387T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181762 | ||||||
chr11:49181783
|
C | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+1366G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181783 | ||||||
chr11:49181935
|
A | G | 82 | a0002c0002t0001g0245a0002c0002t0001g0289a0002c0002t0001g0290others(79): Show | 87 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.920+1214T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49181935 | ||||||
chr11:49182055
|
G | A | 1 | a0002c0003t0001g0059 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.920+1094C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182055 | ||||||
chr11:49182061
|
C | A | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.920+1088G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182061 | ||||||
chr11:49182115
|
G | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+1034C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182115 | ||||||
chr11:49182150
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+999C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182150 | ||||||
chr11:49182253
|
C | T | 12 | a0001c0004t0001g0102a0001c0004t0001g0108a0001c0004t0001g0109others(9): Show | 13 | HG02615.hp1 HG02622.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.920+896G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182253 | ||||||
chr11:49182254
|
A | G | 292 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(289): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.920+895T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182254 | ||||||
chr11:49182310
|
C | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+839G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182310 | ||||||
chr11:49182328
|
C | CA | 74 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(71): Show | 98 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.920+820dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182328 | ||||||
chr11:49182328
|
C | CAA | 84 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0227others(81): Show | 91 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.920+819_920+820dup others(2): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182328 | ||||||
chr11:49182328
|
C | CAAA | 120 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(117): Show | 133 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.920+818_920+820dup others(3): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182328 | ||||||
chr11:49182328
|
C | CAAAA | 41 | a0001c0001t0002g0007a0001c0001t0002g0018a0001c0001t0002g0092others(38): Show | 44 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.920+817_920+820dup others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182328 | ||||||
chr11:49182358
|
G | A | 1 | a0002c0003t0001g0056 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.920+791C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182358 | ||||||
chr11:49182514
|
C | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+635G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182514 | ||||||
chr11:49182524
|
G | C | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.920+625C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182524 | ||||||
chr11:49182545
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.920+604G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182545 | ||||||
chr11:49182565
|
C | T | 142 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(139): Show | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.920+584G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182565 | ||||||
chr11:49182584
|
A | G | 2 | a0001c0001t0002g0117a0001c0001t0002g0177 | 2 | HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.920+565T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182584 | ||||||
chr11:49182633
|
A | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.920+516T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182633 | ||||||
chr11:49182862
|
A | C | 292 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(289): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.920+287T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182862 | ||||||
chr11:49182863
|
A | T | 144 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(141): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.920+286T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182863 | ||||||
chr11:49182892
|
C | T | 1 | a0001c0001t0007g0008 | 3 | HG02109.hp1 HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.920+257G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49182892 | ||||||
chr11:49183017
|
A | G | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+132T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 7/18 | chr11 | 49183017 | ||||||
chr11:49183293
|
C | T | 3 | a0002c0003t0001g0084a0002c0003t0001g0085a0002c0003t0001g0086 | 3 | HG00544.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.827-51G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183293 | ||||||
chr11:49183412
|
A | T | 5 | a0002c0002t0002g0268a0002c0002t0003g0022a0002c0002t0003g0261others(2): Show | 6 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-170T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183412 | ||||||
chr11:49183569
|
G | A | 139 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(136): Show | 155 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.827-327C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183569 | ||||||
chr11:49183578
|
A | G | 1 | a0002c0002t0003g0272 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.827-336T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183578 | ||||||
chr11:49183661
|
C | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.827-419G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183661 | ||||||
chr11:49183709
|
C | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827-467G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183709 | ||||||
chr11:49183851
|
G | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-609C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183851 | ||||||
chr11:49183986
|
A | G | 2 | a0002c0003t0001g0033a0002c0003t0001g0034 | 2 | HG01071.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.827-744T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49183986 | ||||||
chr11:49184082
|
T | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.827-840A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184082 | ||||||
chr11:49184167
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.827-925A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184167 | ||||||
chr11:49184275
|
A | G | 1 | a0002c0003t0002g0049 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.827-1033T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184275 | ||||||
chr11:49184305
|
A | T | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.827-1063T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184305 | ||||||
chr11:49184386
|
T | C | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.827-1144A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184386 | ||||||
chr11:49184439
|
T | G | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.827-1197A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184439 | ||||||
chr11:49184588
|
T | A | 1 | a0001c0001t0002g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.826+1081A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184588 | ||||||
chr11:49184678
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.826+991G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184678 | ||||||
chr11:49184773
|
A | C | 139 | a0002c0002t0001g0245a0002c0002t0001g0289a0002c0002t0001g0290others(136): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.826+896T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184773 | ||||||
chr11:49184937
|
A | G | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.826+732T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49184937 | ||||||
chr11:49185173
|
C | T | 1 | a0002c0002t0001g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.826+496G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185173 | ||||||
chr11:49185305
|
G | T | 3 | a0002c0002t0001g0314a0002c0002t0001g0315a0002c0002t0004g0313 | 3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.826+364C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185305 | ||||||
chr11:49185326
|
G | A | 1 | a0002c0002t0003g0278 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.826+343C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185326 | ||||||
chr11:49185364
|
A | G | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.826+305T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185364 | ||||||
chr11:49185525
|
A | C | 3 | a0002c0002t0001g0314a0002c0002t0001g0315a0002c0002t0004g0313 | 3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.826+144T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185525 | ||||||
chr11:49185580
|
T | C | 1 | a0002c0002t0003g0284 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.826+89A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 6/18 | chr11 | 49185580 | ||||||
chr11:49185909
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.640-54C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49185909 | ||||||
chr11:49185942
|
A | G | 1 | a0002c0002t0001g0300 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.640-87T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49185942 | ||||||
chr11:49186155
|
T | C | 1 | a0001c0001t0005g0204 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.640-300A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186155 | ||||||
chr11:49186224
|
A | T | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.640-369T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186224 | ||||||
chr11:49186267
|
T | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+377A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186267 | ||||||
chr11:49186347
|
A | G | 1 | a0001c0001t0002g0194 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.639+297T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186347 | ||||||
chr11:49186478
|
C | G | 1 | a0001c0001t0001g0321 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.639+166G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186478 | ||||||
chr11:49186617
|
G | GA | 9 | a0002c0002t0003g0023a0002c0002t0003g0269a0002c0002t0003g0270others(6): Show | 10 | HG00558.hp2 HG02040.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.639+26dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186617 | ||||||
chr11:49186626
|
A | T | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+18T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 5/18 | chr11 | 49186626 | ||||||
chr11:49186827
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.514-58C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49186827 | ||||||
chr11:49186962
|
A | G | 1 | a0002c0003t0001g0031 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.514-193T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49186962 | ||||||
chr11:49187031
|
A | C | 1 | a0001c0001t0002g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.514-262T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187031 | ||||||
chr11:49187041
|
C | G | 4 | a0002c0002t0003g0023a0002c0002t0003g0269a0002c0002t0003g0270others(1): Show | 5 | HG02040.hp2 NA18944.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-272G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187041 | ||||||
chr11:49187043
|
CA | C | 24 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 28 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.514-275delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187043 | ||||||
chr11:49187044
|
A | C | 2 | a0001c0001t0001g0241a0002c0003t0001g0060 | 2 | HG02165.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.514-275T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187044 | ||||||
chr11:49187086
|
G | T | 2 | a0001c0001t0002g0106a0001c0001t0002g0107 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.514-317C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187086 | ||||||
chr11:49187097
|
G | C | 1 | a0002c0002t0003g0282 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.514-328C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187097 | ||||||
chr11:49187165
|
G | T | 2 | a0003c0005t0002g0029a0003c0005t0002g0030 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.514-396C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187165 | ||||||
chr11:49187197
|
T | C | 2 | a0001c0001t0002g0098a0001c0001t0002g0178 | 2 | NA18940.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.514-428A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187197 | ||||||
chr11:49187225
|
G | T | 1 | a0002c0003t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.514-456C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187225 | ||||||
chr11:49187232
|
A | C | 1 | a0002c0002t0001g0305 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.514-463T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187232 | ||||||
chr11:49187310
|
G | T | 138 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(135): Show | 152 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.514-541C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187310 | ||||||
chr11:49187316
|
C | T | 139 | a0002c0002t0001g0245a0002c0002t0001g0289a0002c0002t0001g0290others(136): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.514-547G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187316 | ||||||
chr11:49187383
|
C | A | 322 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(319): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.514-614G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187383 | ||||||
chr11:49187395
|
A | G | 1 | a0002c0003t0001g0057 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.514-626T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187395 | ||||||
chr11:49187511
|
T | G | 322 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(319): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.514-742A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187511 | ||||||
chr11:49187713
|
A | T | 1 | a0001c0001t0002g0101 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.514-944T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187713 | ||||||
chr11:49187745
|
G | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-976C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187745 | ||||||
chr11:49187786
|
T | C | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1017A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187786 | ||||||
chr11:49187900
|
T | C | 1 | a0002c0003t0001g0057 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.514-1131A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187900 | ||||||
chr11:49187936
|
T | C | 4 | a0002c0003t0001g0058a0002c0003t0001g0059a0002c0003t0001g0074others(1): Show | 4 | HG03704.hp2 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.514-1167A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49187936 | ||||||
chr11:49188019
|
T | C | 2 | a0002c0002t0001g0305a0002c0002t0001g0306 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.514-1250A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188019 | ||||||
chr11:49188051
|
C | G | 5 | a0002c0002t0002g0268a0002c0002t0003g0022a0002c0002t0003g0261others(2): Show | 6 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.514-1282G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188051 | ||||||
chr11:49188096
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.514-1327C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188096 | ||||||
chr11:49188170
|
A | T | 141 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(138): Show | 165 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.514-1401T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188170 | ||||||
chr11:49188202
|
G | T | 1 | a0002c0003t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.514-1433C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188202 | ||||||
chr11:49188208
|
G | A | 1 | a0002c0003t0001g0039 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.514-1439C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188208 | ||||||
chr11:49188282
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.514-1513C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188282 | ||||||
chr11:49188390
|
T | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1621A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188390 | ||||||
chr11:49188391
|
G | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1622C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188391 | ||||||
chr11:49188487
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.514-1718G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188487 | ||||||
chr11:49188512
|
C | CA | 221 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0322others(218): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.514-1744dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188512 | ||||||
chr11:49188512
|
C | CAA | 57 | a0001c0001t0002g0194a0001c0001t0002g0205a0001c0001t0014g0180others(54): Show | 75 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.514-1745_514-1744d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188512 | ||||||
chr11:49188642
|
G | T | 292 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(289): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.514-1873C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188642 | ||||||
chr11:49188667
|
C | T | 2 | a0003c0005t0002g0029a0003c0005t0002g0030 | 2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.514-1898G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188667 | ||||||
chr11:49188695
|
T | A | 3 | a0002c0002t0001g0314a0002c0002t0001g0315a0002c0002t0004g0313 | 3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.514-1926A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188695 | ||||||
chr11:49188972
|
A | G | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.514-2203T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49188972 | ||||||
chr11:49189003
|
T | C | 4 | a0002c0002t0003g0021a0002c0002t0003g0247a0002c0002t0003g0248others(1): Show | 5 | HG02258.hp1 HG02486.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2234A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189003 | ||||||
chr11:49189042
|
C | G | 1 | a0001c0001t0002g0200 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.514-2273G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189042 | ||||||
chr11:49189155
|
C | T | 1 | a0001c0001t0002g0113 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.514-2386G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189155 | ||||||
chr11:49189186
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.514-2417G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189186 | ||||||
chr11:49189538
|
C | T | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-2769G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189538 | ||||||
chr11:49189645
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.514-2876C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189645 | ||||||
chr11:49189676
|
T | C | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.514-2907A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189676 | ||||||
chr11:49189998
|
C | G | 1 | a0001c0001t0002g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.513+2795G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49189998 | ||||||
chr11:49190000
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.513+2793G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49190000 | ||||||
chr11:49190252
|
A | G | 280 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0002g0002others(277): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.513+2541T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49190252 | ||||||
chr11:49190313
|
A | C | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.513+2480T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49190313 | ||||||
chr11:49190704
|
T | C | 3 | a0001c0001t0002g0182a0001c0001t0002g0183a0001c0001t0012g0184 | 3 | HG03942.hp2 NA18952.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.513+2089A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49190704 | ||||||
chr11:49191106
|
C | G | 1 | a0002c0002t0001g0245 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.513+1687G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191106 | ||||||
chr11:49191135
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.513+1658G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191135 | ||||||
chr11:49191140
|
T | C | 1 | a0004c0006t0004g0320 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.513+1653A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191140 | ||||||
chr11:49191147
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(1): Show | 5 | HG01515.hp2 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1646C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191147 | ||||||
chr11:49191375
|
C | T | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+1418G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191375 | ||||||
chr11:49191410
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.513+1383T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191410 | ||||||
chr11:49191456
|
A | C | 1 | a0004c0006t0004g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.513+1337T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191456 | ||||||
chr11:49191650
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.513+1143C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191650 | ||||||
chr11:49191694
|
T | C | 1 | a0002c0002t0004g0313 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.513+1099A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191694 | ||||||
chr11:49191729
|
G | A | 5 | a0002c0003t0001g0061a0002c0003t0001g0062a0002c0003t0001g0063others(2): Show | 5 | HG00099.hp2 HG01433.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1064C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191729 | ||||||
chr11:49191735
|
TCA | T | 139 | a0002c0002t0001g0245a0002c0002t0001g0289a0002c0002t0001g0290others(136): Show | 162 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.513+1056_513+1057d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191735 | ||||||
chr11:49191793
|
G | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+1000C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191793 | ||||||
chr11:49191935
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.513+858C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191935 | ||||||
chr11:49191952
|
C | T | 33 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(30): Show | 37 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.513+841G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49191952 | ||||||
chr11:49192294
|
G | T | 3 | a0002c0002t0001g0314a0002c0002t0001g0315a0002c0002t0004g0313 | 3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.513+499C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192294 | ||||||
chr11:49192325
|
T | C | 4 | a0002c0002t0001g0245a0002c0002t0001g0301a0002c0002t0001g0302others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+468A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192325 | ||||||
chr11:49192354
|
G | A | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+439C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192354 | ||||||
chr11:49192411
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.513+382A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192411 | ||||||
chr11:49192496
|
C | A | 187 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(184): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.513+297G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192496 | ||||||
chr11:49192692
|
T | C | 1 | a0001c0001t0002g0186 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.513+101A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 4/18 | chr11 | 49192692 | ||||||
chr11:49192947
|
G | A | 187 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(184): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.412-53C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49192947 | ||||||
chr11:49192980
|
T | A | 1 | a0003c0005t0002g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.412-86A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49192980 | ||||||
chr11:49193016
|
T | G | 9 | a0001c0001t0002g0105a0001c0001t0002g0187a0001c0001t0002g0188others(6): Show | 9 | NA18948.hp1 NA18953.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-122A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193016 | ||||||
chr11:49193464
|
C | T | 61 | a0002c0003t0001g0003a0002c0003t0001g0004a0002c0003t0001g0013others(58): Show | 66 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.412-570G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193464 | ||||||
chr11:49193482
|
A | G | 1 | a0003c0005t0002g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.412-588T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193482 | ||||||
chr11:49193552
|
C | A | 4 | a0002c0002t0001g0308a0002c0002t0001g0309a0002c0002t0001g0310others(1): Show | 4 | HG02723.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-658G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193552 | ||||||
chr11:49193681
|
A | C | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-787T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193681 | ||||||
chr11:49193736
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412-842G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193736 | ||||||
chr11:49193738
|
A | G | 1 | a0001c0001t0002g0197 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.412-844T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193738 | ||||||
chr11:49193879
|
G | A | 142 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(139): Show | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.412-985C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193879 | ||||||
chr11:49193936
|
G | A | 1 | a0005c0007t0009g0243 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.412-1042C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193936 | ||||||
chr11:49193962
|
A | T | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-1068T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193962 | ||||||
chr11:49193987
|
G | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.412-1093C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49193987 | ||||||
chr11:49194003
|
C | G | 142 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(139): Show | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.412-1109G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194003 | ||||||
chr11:49194078
|
G | C | 2 | a0001c0001t0002g0195a0001c0001t0002g0196 | 2 | NA19002.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.412-1184C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194078 | ||||||
chr11:49194081
|
G | T | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.412-1187C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194081 | ||||||
chr11:49194083
|
C | T | 85 | a0002c0002t0001g0245a0002c0002t0001g0289a0002c0002t0001g0290others(82): Show | 90 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.412-1189G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194083 | ||||||
chr11:49194087
|
C | T | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-1193G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194087 | ||||||
chr11:49194132
|
C | CA | 100 | a0001c0001t0001g0237a0001c0001t0002g0099a0001c0001t0002g0105others(97): Show | 107 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.412-1239dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194132 | ||||||
chr11:49194132
|
C | CAA | 10 | a0002c0002t0001g0296a0002c0002t0001g0315a0002c0003t0001g0040others(7): Show | 10 | HG00621.hp2 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.412-1240_412-1239d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194132 | ||||||
chr11:49194132
|
CA | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0218a0001c0001t0001g0219others(8): Show | 13 | HG01192.hp1 HG01515.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.412-1239delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194132 | ||||||
chr11:49194238
|
A | G | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412-1344T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194238 | ||||||
chr11:49194296
|
T | C | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.412-1402A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194296 | ||||||
chr11:49194316
|
A | C | 1 | a0003c0005t0006g0326 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.412-1422T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194316 | ||||||
chr11:49194405
|
T | A | 1 | a0001c0001t0002g0206 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.412-1511A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194405 | ||||||
chr11:49194538
|
A | C | 3 | a0001c0001t0002g0095a0001c0001t0002g0106a0001c0001t0002g0107 | 3 | HG02280.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.412-1644T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194538 | ||||||
chr11:49194604
|
G | A | 2 | a0002c0002t0003g0256a0002c0002t0003g0257 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.412-1710C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194604 | ||||||
chr11:49194702
|
G | T | 1 | a0001c0001t0002g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.412-1808C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194702 | ||||||
chr11:49194869
|
A | G | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.412-1975T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194869 | ||||||
chr11:49194962
|
G | T | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.412-2068C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49194962 | ||||||
chr11:49195019
|
C | A | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.412-2125G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195019 | ||||||
chr11:49195028
|
T | C | 1 | a0001c0001t0002g0207 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.412-2134A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195028 | ||||||
chr11:49195059
|
C | G | 4 | a0002c0002t0001g0245a0002c0002t0001g0301a0002c0002t0001g0302others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.412-2165G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195059 | ||||||
chr11:49195147
|
C | T | 148 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(145): Show | 173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.412-2253G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195147 | ||||||
chr11:49195249
|
G | T | 1 | a0001c0001t0002g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.412-2355C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195249 | ||||||
chr11:49195454
|
A | G | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.412-2560T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195454 | ||||||
chr11:49195581
|
A | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-2687T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195581 | ||||||
chr11:49195614
|
A | C | 57 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316others(54): Show | 76 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.412-2720T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195614 | ||||||
chr11:49195675
|
GA | G | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.412-2782delT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195675 | ||||||
chr11:49195759
|
A | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-2865T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195759 | ||||||
chr11:49195817
|
A | G | 1 | a0001c0001t0002g0104 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.412-2923T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195817 | ||||||
chr11:49195840
|
A | C | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-2946T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49195840 | ||||||
chr11:49196010
|
C | T | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-3116G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196010 | ||||||
chr11:49196013
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.412-3119C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196013 | ||||||
chr11:49196062
|
G | A | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.412-3168C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196062 | ||||||
chr11:49196068
|
T | G | 59 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316others(56): Show | 78 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.412-3174A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196068 | ||||||
chr11:49196282
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.412-3388C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196282 | ||||||
chr11:49196320
|
G | T | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.412-3426C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196320 | ||||||
chr11:49196362
|
A | G | 1 | a0002c0003t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.412-3468T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196362 | ||||||
chr11:49196625
|
A | AT | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.411+3629_411+3630i others(3): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196625 | ||||||
chr11:49196661
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.411+3594G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196661 | ||||||
chr11:49196662
|
G | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+3593C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196662 | ||||||
chr11:49196694
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.411+3561T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196694 | ||||||
chr11:49196827
|
A | G | 1 | a0002c0002t0003g0248 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411+3428T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196827 | ||||||
chr11:49196874
|
T | C | 1 | a0001c0001t0001g0027 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.411+3381A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196874 | ||||||
chr11:49196892
|
G | C | 1 | a0001c0001t0001g0027 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.411+3363C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49196892 | ||||||
chr11:49197011
|
A | G | 1 | a0002c0002t0001g0290 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.411+3244T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197011 | ||||||
chr11:49197035
|
C | T | 1 | a0002c0003t0013g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.411+3220G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197035 | ||||||
chr11:49197167
|
A | G | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+3088T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197167 | ||||||
chr11:49197307
|
T | C | 61 | a0002c0003t0001g0003a0002c0003t0001g0004a0002c0003t0001g0013others(58): Show | 66 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.411+2948A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197307 | ||||||
chr11:49197551
|
T | C | 1 | a0003c0005t0002g0030 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.411+2704A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197551 | ||||||
chr11:49197876
|
T | C | 4 | a0002c0003t0001g0068a0002c0003t0001g0069a0002c0003t0001g0070others(1): Show | 4 | HG01361.hp1 HG01952.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+2379A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49197876 | ||||||
chr11:49198173
|
C | G | 187 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(184): Show | 218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.411+2082G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198173 | ||||||
chr11:49198179
|
A | G | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.411+2076T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198179 | ||||||
chr11:49198246
|
C | A | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+2009G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198246 | ||||||
chr11:49198373
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.411+1882A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198373 | ||||||
chr11:49198374
|
A | C | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.411+1881T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198374 | ||||||
chr11:49198400
|
T | C | 1 | a0001c0001t0002g0208 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.411+1855A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198400 | ||||||
chr11:49198407
|
G | A | 5 | a0002c0002t0002g0268a0002c0002t0003g0022a0002c0002t0003g0261others(2): Show | 6 | HG01496.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+1848C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198407 | ||||||
chr11:49198435
|
T | C | 1 | a0002c0003t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.411+1820A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198435 | ||||||
chr11:49198440
|
C | CCACTGCA others(15): Show |
4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+1793_411+1814d others(24): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198440 | ||||||
chr11:49198481
|
C | CA | 136 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0290others(133): Show | 160 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.411+1773dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198481 | ||||||
chr11:49198481
|
C | CAA | 8 | a0002c0002t0001g0289a0002c0002t0001g0303a0002c0002t0003g0286others(5): Show | 8 | HG01433.hp1 HG02280.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+1772_411+1773d others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198481 | ||||||
chr11:49198490
|
C | A | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.411+1765G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198490 | ||||||
chr11:49198542
|
T | C | 1 | a0002c0002t0003g0287 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.411+1713A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198542 | ||||||
chr11:49198687
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(7): Show | 14 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.411+1568G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198687 | ||||||
chr11:49198740
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.411+1515T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198740 | ||||||
chr11:49198801
|
G | A | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.411+1454C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198801 | ||||||
chr11:49198921
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG02015.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.411+1334A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198921 | ||||||
chr11:49198960
|
A | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+1295T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49198960 | ||||||
chr11:49199037
|
C | T | 1 | a0002c0003t0001g0045 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.411+1218G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199037 | ||||||
chr11:49199038
|
A | G | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.411+1217T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199038 | ||||||
chr11:49199057
|
G | A | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.411+1198C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199057 | ||||||
chr11:49199185
|
A | G | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+1070T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199185 | ||||||
chr11:49199271
|
G | A | 1 | a0003c0005t0002g0029 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.411+984C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199271 | ||||||
chr11:49199315
|
T | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+940A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199315 | ||||||
chr11:49199503
|
G | C | 25 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(22): Show | 29 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.411+752C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199503 | ||||||
chr11:49199544
|
C | T | 142 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(139): Show | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.411+711G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199544 | ||||||
chr11:49199662
|
C | T | 1 | a0001c0001t0002g0101 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.411+593G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199662 | ||||||
chr11:49199689
|
T | A | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+566A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199689 | ||||||
chr11:49199708
|
C | T | 2 | a0005c0007t0009g0243a0005c0007t0009g0244 | 2 | HG01346.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.411+547G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199708 | ||||||
chr11:49199839
|
A | C | 1 | a0001c0001t0002g0100 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.411+416T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199839 | ||||||
chr11:49199860
|
G | A | 3 | a0002c0002t0001g0314a0002c0002t0001g0315a0002c0002t0004g0313 | 3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.411+395C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199860 | ||||||
chr11:49199936
|
T | C | 55 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(52): Show | 73 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.411+319A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49199936 | ||||||
chr11:49200233
|
T | C | 1 | a0001c0001t0002g0209 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.411+22A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 3/18 | chr11 | 49200233 | ||||||
chr11:49201197
|
GT | G | 54 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(51): Show | 72 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.225-757delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201197 | ||||||
chr11:49201255
|
G | GAT | 85 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(82): Show | 90 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.225-816_225-815dup others(2): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | ||||||
chr11:49201255
|
G | GATAT | 72 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(69): Show | 95 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.225-818_225-815dup others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | ||||||
chr11:49201255
|
G | GATATAT | 13 | a0001c0001t0001g0230a0001c0001t0001g0231a0002c0002t0001g0245others(10): Show | 14 | HG01496.hp1 HG01943.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.225-820_225-815dup others(6): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | ||||||
chr11:49201255
|
G | GATATATA others(1): Show |
9 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(6): Show | 9 | NA18942.hp2 NA18964.hp1 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.225-822_225-815dup others(8): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | ||||||
chr11:49201255
|
G | GATATATA others(3): Show |
3 | a0002c0002t0003g0261a0004c0006t0004g0319a0004c0006t0004g0320 | 3 | HG02818.hp1 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.225-824_225-815dup others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | ||||||
chr11:49201255
|
G | GATATATA others(5): Show |
1 | a0004c0006t0004g0318 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.225-826_225-815dup others(12): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | ||||||
chr11:49201255
|
G | GATATATA others(7): Show |
1 | a0004c0006t0004g0026 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.225-828_225-815dup others(14): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201255 | ||||||
chr11:49201282
|
C | A | 1 | a0002c0002t0003g0299 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.225-841G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201282 | ||||||
chr11:49201284
|
T | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.225-843A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201284 | ||||||
chr11:49201354
|
T | C | 11 | a0002c0002t0001g0289a0002c0002t0001g0290a0002c0002t0001g0291others(8): Show | 11 | HG01109.hp2 HG02486.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.225-913A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201354 | ||||||
chr11:49201384
|
C | T | 18 | a0002c0002t0003g0010a0002c0002t0003g0021a0002c0002t0003g0247others(15): Show | 21 | HG01243.hp1 HG01257.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.225-943G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201384 | ||||||
chr11:49201433
|
AT | A | 44 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0011others(41): Show | 61 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.225-993delA | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201433 | ||||||
chr11:49201739
|
A | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0220others(1): Show | 4 | HG02965.hp1 HG03041.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-1298T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49201739 | ||||||
chr11:49202011
|
A | C | 1 | a0001c0001t0002g0098 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.225-1570T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202011 | ||||||
chr11:49202534
|
G | T | 142 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(139): Show | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.225-2093C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202534 | ||||||
chr11:49202679
|
G | A | 182 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(179): Show | 212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.225-2238C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202679 | ||||||
chr11:49202689
|
C | T | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.225-2248G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202689 | ||||||
chr11:49202704
|
T | G | 2 | a0001c0001t0001g0323a0001c0001t0015g0324 | 2 | HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.225-2263A>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49202704 | ||||||
chr11:49203135
|
ATATTCAA others(13): Show |
A | 1 | a0002c0002t0003g0288 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.225-2714_225-2695d others(22): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203135 | ||||||
chr11:49203333
|
G | A | 1 | a0001c0010t0002g0210 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.224+2734C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203333 | ||||||
chr11:49203543
|
T | A | 1 | a0001c0001t0002g0211 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.224+2524A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203543 | ||||||
chr11:49203617
|
C | T | 3 | a0001c0001t0005g0096a0001c0001t0005g0097a0001c0001t0005g0212 | 3 | HG00099.hp1 HG01123.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.224+2450G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203617 | ||||||
chr11:49203699
|
G | A | 2 | a0002c0003t0001g0042a0002c0003t0001g0043 | 2 | NA19001.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.224+2368C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203699 | ||||||
chr11:49203764
|
T | A | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.224+2303A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203764 | ||||||
chr11:49203800
|
G | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.224+2267C>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203800 | ||||||
chr11:49203832
|
C | G | 1 | a0002c0002t0008g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.224+2235G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203832 | ||||||
chr11:49203974
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.224+2093T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49203974 | ||||||
chr11:49204006
|
G | T | 1 | a0002c0002t0003g0246 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.224+2061C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204006 | ||||||
chr11:49204227
|
A | T | 17 | a0002c0002t0003g0010a0002c0002t0003g0021a0002c0002t0003g0247others(14): Show | 20 | HG01243.hp1 HG01257.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.224+1840T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204227 | ||||||
chr11:49204261
|
C | T | 3 | a0002c0002t0001g0305a0002c0002t0001g0306a0002c0011t0001g0312 | 3 | HG01109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.224+1806G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204261 | ||||||
chr11:49204336
|
T | C | 1 | a0001c0001t0005g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224+1731A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204336 | ||||||
chr11:49204610
|
C | T | 55 | a0002c0002t0002g0268a0002c0002t0003g0001a0002c0002t0003g0010others(52): Show | 73 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.224+1457G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204610 | ||||||
chr11:49204632
|
A | G | 142 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(139): Show | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.224+1435T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204632 | ||||||
chr11:49204636
|
C | T | 3 | a0003c0005t0006g0028a0003c0005t0006g0326a0003c0005t0006g0327 | 4 | HG01884.hp1 HG02055.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+1431G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204636 | ||||||
chr11:49204745
|
T | A | 3 | a0002c0003t0001g0084a0002c0003t0001g0085a0002c0003t0001g0086 | 3 | HG00544.hp2 HG00733.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.224+1322A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49204745 | ||||||
chr11:49205076
|
G | T | 1 | a0004c0006t0004g0026 | 2 | HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.224+991C>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205076 | ||||||
chr11:49205131
|
G | A | 3 | a0002c0002t0003g0297a0002c0002t0003g0298a0002c0002t0003g0299 | 3 | HG02451.hp2 HG02895.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.224+936C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205131 | ||||||
chr11:49205164
|
A | G | 1 | a0001c0001t0002g0094 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.224+903T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205164 | ||||||
chr11:49205294
|
G | A | 1 | a0002c0002t0001g0315 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.224+773C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205294 | ||||||
chr11:49205333
|
C | T | 5 | a0003c0005t0002g0029a0003c0005t0002g0030a0003c0005t0006g0028others(2): Show | 6 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.224+734G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205333 | ||||||
chr11:49205557
|
G | A | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.224+510C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205557 | ||||||
chr11:49205936
|
G | A | 144 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(141): Show | 168 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.224+131C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49205936 | ||||||
chr11:49206018
|
T | A | 2 | a0001c0001t0002g0214a0001c0008t0002g0213 | 2 | HG01168.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.224+49A>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 2/18 | chr11 | 49206018 | ||||||
chr11:49206332
|
A | C | 1 | a0002c0002t0003g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.119-160T>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206332 | ||||||
chr11:49206394
|
C | T | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-222G>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206394 | ||||||
chr11:49206500
|
T | C | 3 | a0002c0002t0001g0314a0002c0002t0001g0315a0002c0002t0004g0313 | 3 | HG02145.hp1 HG02451.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.119-328A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206500 | ||||||
chr11:49206505
|
T | C | 1 | a0001c0001t0002g0215 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.119-333A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206505 | ||||||
chr11:49206555
|
A | G | 6 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(3): Show | 6 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-383T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206555 | ||||||
chr11:49206572
|
CAAAT | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0300a0002c0002t0001g0316 | 4 | HG01891.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-404_119-401del others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206572 | ||||||
chr11:49206835
|
T | C | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-663A>G | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49206835 | ||||||
chr11:49207061
|
C | G | 148 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(145): Show | 173 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.119-889G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207061 | ||||||
chr11:49207252
|
A | G | 1 | a0002c0002t0003g0246 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.118+1040T>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207252 | ||||||
chr11:49207449
|
G | A | 142 | a0002c0002t0001g0025a0002c0002t0001g0245a0002c0002t0001g0289others(139): Show | 166 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.118+843C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207449 | ||||||
chr11:49207678
|
C | A | 1 | a0001c0001t0002g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.118+614G>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207678 | ||||||
chr11:49207688
|
G | A | 1 | a0001c0001t0002g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.118+604C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207688 | ||||||
chr11:49207883
|
C | G | 1 | a0005c0007t0009g0243 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.118+409G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207883 | ||||||
chr11:49207932
|
T | TA | 4 | a0004c0006t0004g0026a0004c0006t0004g0318a0004c0006t0004g0319others(1): Show | 5 | HG02615.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+359dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207932 | ||||||
chr11:49207933
|
A | T | 4 | a0002c0002t0001g0245a0002c0002t0001g0301a0002c0002t0001g0302others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+359T>A | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207933 | ||||||
chr11:49207936
|
AAAAC | A | 34 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(31): Show | 39 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.118+352_118+355del others(4): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207936 | ||||||
chr11:49207948
|
C | CAAACA | 15 | a0002c0003t0001g0031a0002c0003t0001g0032a0002c0003t0001g0033others(12): Show | 15 | HG01071.hp1 HG01346.hp2 HG02602.hp1 others(12): Show |
intron_variant | MODIFIER | c.118+339_118+343dup others(5): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207948 | ||||||
chr11:49207948
|
C | CAAACAAA others(3): Show |
111 | a0002c0002t0001g0245a0002c0002t0001g0289a0002c0002t0001g0290others(108): Show | 134 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.118+334_118+343dup others(10): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207948 | ||||||
chr11:49207948
|
C | CAAACAAA others(8): Show |
17 | a0002c0002t0001g0025a0002c0002t0001g0301a0002c0002t0001g0302others(14): Show | 18 | HG01109.hp2 HG01257.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.118+329_118+343dup others(15): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207948 | ||||||
chr11:49207948
|
C | CAAACAAA others(13): Show |
1 | a0002c0002t0001g0317 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.118+324_118+343dup others(20): Show |
FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207948 | ||||||
chr11:49207978
|
C | CA | 6 | a0001c0001t0015g0324a0002c0003t0001g0087a0004c0006t0004g0026others(3): Show | 7 | HG01515.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.118+313dupT | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49207978 | ||||||
chr11:49208226
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 6 | HG01192.hp1 HG01515.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+66C>T | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49208226 | ||||||
chr11:49208281
|
C | G | 60 | a0002c0003t0001g0003a0002c0003t0001g0004a0002c0003t0001g0013others(57): Show | 65 | HG00099.hp2 HG00544.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.118+11G>C | FOLH1 | ENSG00000086205.18 | transcript | ENST00000256999.7 | protein_coding | 1/18 | chr11 | 49208281 |