geneid | 3172 |
---|---|
ensemblid | ENSG00000101076.20 |
hgncid | 5024 |
symbol | HNF4A |
name | hepatocyte nuclear factor 4 alpha |
refseq_nuc | NM_175914.5 |
refseq_prot | NP_787110.2 |
ensembl_nuc | ENST00000316673.9 |
ensembl_prot | ENSP00000315180.4 |
mane_status | MANE Select |
chr | chr20 |
start | 44355699 |
end | 44432845 |
strand | + |
ver | v1.2 |
region | chr20:44355699-44432845 |
region5000 | chr20:44350699-44437845 |
regionname0 | HNF4A_chr20_44355699_44432845 |
regionname5000 | HNF4A_chr20_44350699_44437845 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 452 | 309 | 87 | 51 | 114 | 18 | 37 | 80 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0002 | 0/0 | 452 | 7 | 0 | 3 | 2 | 0 | 2 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0003 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0004 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0005 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0006 | 0/0 | 452 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0007 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0008 | 0/0 | 452 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
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 | 1/1 | 1359 | 302 | 83 | 49 | 113 | 18 | 37 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0002 | 0/0 | 1359 | 7 | 0 | 3 | 2 | 0 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0003 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0004 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0005 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0006 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0007 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0008 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0009 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0010 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0011 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0012 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0013 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
c0014 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
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 | 0/0 | 3288 | 49 | 12 | 16 | 7 | 6 | 8 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0002 | 0/0 | 3288 | 34 | 2 | 2 | 21 | 1 | 8 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0003 | 0/0 | 3269 | 28 | 1 | 2 | 19 | 3 | 3 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0004 | 0/0 | 3288 | 22 | 2 | 1 | 19 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0005 | 0/0 | 3288 | 13 | 1 | 3 | 5 | 2 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0006 | 0/0 | 3288 | 9 | 0 | 6 | 1 | 1 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0007 | 0/0 | 3288 | 8 | 1 | 4 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0008 | 0/0 | 3287 | 8 | 5 | 3 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0009 | 0/0 | 3267 | 5 | 0 | 0 | 0 | 0 | 5 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0010 | 0/0 | 3287 | 5 | 5 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0011 | 0/0 | 3289 | 5 | 3 | 1 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0012 | 0/0 | 3288 | 4 | 4 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0013 | 0/0 | 3287 | 4 | 3 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0014 | 0/0 | 3269 | 4 | 0 | 0 | 4 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0015 | 0/0 | 3280 | 4 | 0 | 0 | 4 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0016 | 0/0 | 3268 | 3 | 0 | 0 | 2 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0017 | 0/0 | 3279 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0018 | 0/0 | 3288 | 3 | 2 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0019 | 0/0 | 3286 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0020 | 0/0 | 3280 | 3 | 0 | 0 | 2 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0021 | 0/0 | 3288 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0022 | 0/0 | 3287 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0023 | 0/0 | 3268 | 3 | 2 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0024 | 0/0 | 3270 | 3 | 0 | 1 | 1 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0025 | 0/0 | 3288 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0026 | 0/0 | 3259 | 2 | 0 | 0 | 0 | 1 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0027 | 0/0 | 3268 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0028 | 0/0 | 3280 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0029 | 0/0 | 3286 | 2 | 0 | 0 | 0 | 2 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0030 | 0/0 | 3272 | 2 | 0 | 0 | 0 | 0 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0031 | 0/0 | 3287 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0032 | 0/0 | 3280 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0033 | 0/0 | 3287 | 2 | 1 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0034 | 0/0 | 3289 | 2 | 1 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0035 | 0/0 | 3289 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0036 | 0/0 | 3268 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0037 | 0/0 | 3287 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0038 | 0/0 | 3288 | 2 | 1 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0039 | 0/0 | 3280 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0040 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0041 | 0/0 | 3268 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0042 | 0/0 | 3269 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0043 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0044 | 0/0 | 3287 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0045 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0046 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0047 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0048 | 0/0 | 3261 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0049 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0050 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0051 | 0/0 | 3288 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0052 | 0/0 | 3278 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0053 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0054 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0055 | 0/0 | 3280 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0056 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0057 | 0/0 | 3269 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0058 | 0/0 | 3269 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0059 | 0/0 | 3280 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0060 | 0/0 | 3289 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0061 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0062 | 0/0 | 3269 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0063 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0064 | 0/0 | 3268 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0065 | 0/0 | 3269 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0066 | 0/0 | 3287 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0067 | 0/0 | 3287 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0068 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0069 | 0/1 | 3278 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0070 | 0/0 | 3280 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0071 | 0/0 | 3281 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0072 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0073 | 0/0 | 3280 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0074 | 1/0 | 3287 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0075 | 0/0 | 3287 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0076 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0077 | 0/0 | 3286 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0078 | 0/0 | 3287 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0079 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0080 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0081 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0082 | 0/0 | 3269 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0083 | 0/0 | 3176 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0084 | 0/0 | 3287 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0085 | 0/0 | 3288 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0086 | 0/0 | 3280 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0087 | 0/0 | 3287 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0088 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0089 | 0/0 | 3286 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0090 | 0/0 | 3287 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0091 | 0/0 | 3280 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0092 | 0/0 | 3288 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0093 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0094 | 0/0 | 3261 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0095 | 0/0 | 3269 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0096 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0097 | 0/0 | 3431 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0098 | 0/0 | 3269 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0099 | 0/0 | 3268 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0100 | 0/0 | 3289 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0101 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
t0102 | 0/0 | 3288 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
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 | 2 | 0 | 1 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
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 | 1/1 | 1359 | 302 | 83 | 49 | 113 | 18 | 37 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0003 | 0/0 | 1359 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0009 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0011 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0012 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0013 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0014 | 0/0 | 1359 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0002c0002 | 0/0 | 1359 | 7 | 0 | 3 | 2 | 0 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0003c0004 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0004c0010 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0005c0006 | 0/0 | 1359 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0006c0007 | 0/0 | 1359 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0007c0008 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0008c0005 | 0/0 | 1359 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4646 | 45 | 12 | 14 | 6 | 6 | 7 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0002 | 0/0 | 4646 | 33 | 2 | 2 | 21 | 1 | 7 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0003 | 0/0 | 4627 | 28 | 1 | 2 | 19 | 3 | 3 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0004 | 0/0 | 4646 | 21 | 2 | 1 | 18 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0005 | 0/0 | 4646 | 12 | 1 | 3 | 4 | 2 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0006 | 0/0 | 4646 | 9 | 0 | 6 | 1 | 1 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0007 | 0/0 | 4646 | 7 | 1 | 3 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0008 | 0/0 | 4645 | 7 | 4 | 3 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0009 | 0/0 | 4625 | 5 | 0 | 0 | 0 | 0 | 5 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0010 | 0/0 | 4645 | 4 | 4 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0011 | 0/0 | 4647 | 5 | 3 | 1 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0012 | 0/0 | 4646 | 4 | 4 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0013 | 0/0 | 4645 | 4 | 3 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0014 | 0/0 | 4627 | 4 | 0 | 0 | 4 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0015 | 0/0 | 4638 | 4 | 0 | 0 | 4 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0016 | 0/0 | 4626 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0017 | 0/0 | 4637 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0018 | 0/0 | 4646 | 3 | 2 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0019 | 0/0 | 4644 | 3 | 3 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0020 | 0/0 | 4638 | 3 | 0 | 0 | 2 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0021 | 0/0 | 4646 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0022 | 0/0 | 4645 | 3 | 0 | 0 | 3 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0023 | 0/0 | 4626 | 2 | 1 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0024 | 0/0 | 4628 | 3 | 0 | 1 | 1 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0025 | 0/0 | 4646 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0026 | 0/0 | 4617 | 2 | 0 | 0 | 0 | 1 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0027 | 0/0 | 4626 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0028 | 0/0 | 4638 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0029 | 0/0 | 4644 | 2 | 0 | 0 | 0 | 2 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0030 | 0/0 | 4630 | 2 | 0 | 0 | 0 | 0 | 2 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0031 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0032 | 0/0 | 4638 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0033 | 0/0 | 4645 | 2 | 1 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0034 | 0/0 | 4647 | 2 | 1 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0035 | 0/0 | 4647 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0036 | 0/0 | 4626 | 2 | 0 | 0 | 2 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0037 | 0/0 | 4645 | 2 | 2 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0038 | 0/0 | 4646 | 2 | 1 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0039 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0040 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0041 | 0/0 | 4626 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0042 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0043 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0044 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0045 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0046 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0047 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0048 | 0/0 | 4619 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0049 | 0/0 | 4625 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0050 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0051 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0052 | 0/0 | 4636 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0053 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0054 | 0/0 | 4646 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0055 | 0/0 | 4638 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0056 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0057 | 0/0 | 4627 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0059 | 0/0 | 4638 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0060 | 0/0 | 4647 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0061 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0062 | 0/0 | 4627 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0064 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0065 | 0/0 | 4627 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0067 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0068 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0069 | 0/1 | 4636 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0071 | 0/0 | 4639 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0072 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0073 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0074 | 1/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0075 | 0/0 | 4645 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0076 | 0/0 | 4644 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0077 | 0/0 | 4644 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0078 | 0/0 | 4645 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0079 | 0/0 | 4646 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0081 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0083 | 0/0 | 4534 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0084 | 0/0 | 4645 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0085 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0086 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0087 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0088 | 0/0 | 4637 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0089 | 0/0 | 4644 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0090 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0091 | 0/0 | 4638 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0092 | 0/0 | 4646 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0094 | 0/0 | 4619 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0095 | 0/0 | 4627 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0096 | 0/0 | 4625 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0097 | 0/0 | 4789 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0098 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0099 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0100 | 0/0 | 4647 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0101 | 0/0 | 4637 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0001t0102 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0003t0063 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0003t0066 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0009t0082 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0011t0080 | 0/0 | 4637 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0012t0008 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0013t0010 | 0/0 | 4645 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0001c0014t0070 | 0/0 | 4638 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0002c0002t0001 | 0/0 | 4646 | 4 | 0 | 2 | 1 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0002c0002t0002 | 0/0 | 4646 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0002c0002t0004 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0002c0002t0007 | 0/0 | 4646 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0003c0004t0058 | 0/0 | 4627 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0004c0010t0093 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0005c0006t0023 | 0/0 | 4626 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0006c0007t0016 | 0/0 | 4626 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0007c0008t0005 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
a0008c0005t0025 | 0/0 | 4646 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | copy fasta | chr20 | 44350699 | 44437845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0006g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0006g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0006g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0007g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0007g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0007g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0008g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0008g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0009g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0009g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0009g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0009g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0010g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0011g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0011g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0012g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0012g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0013g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0013g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0013g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0014g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0014g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0014g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0014g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0015g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0015g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0015g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0016g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0016g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0017g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0017g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0017g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0018g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0018g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0019g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0019g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0020g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0020g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0020g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0021g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0021g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0021g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0022g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0022g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0022g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0023g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0023g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0024g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0024g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0024g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0025g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0025g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0026g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0026g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0027g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0027g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0028g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0028g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0029g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0029g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0030g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0030g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0031g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0031g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0032g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0032g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0033g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0033g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0034g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0034g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0035g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0035g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0036g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0036g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0037g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0037g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0038g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0038g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0039g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0040g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0041g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0042g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0043g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0044g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0045g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0046g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0047g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0048g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0049g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0050g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0051g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0052g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0053g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0054g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0055g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0056g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0057g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0059g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0060g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0061g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0062g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0064g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0065g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0067g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0068g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0069g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0071g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0072g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0073g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0074g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0075g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0076g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0077g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0078g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0079g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0081g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0083g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0084g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0085g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0086g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0087g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0088g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0089g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0090g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0091g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0092g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0094g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0095g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0096g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0097g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0098g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0099g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0100g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0101g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0001t0102g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0003t0063g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0003t0066g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0009t0082g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0011t0080g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0012t0008g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0013t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0001c0014t0070g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0002c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0002c0002t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0003c0004t0058g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0004c0010t0093g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0005c0006t0023g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0006c0007t0016g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0007c0008t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
a0008c0005t0025g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0013 | g0184 | EUR | GBR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0095 | EUR | GBR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0270 | EUR | GBR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00280 | hp1 | a0001 | c0001 | t0026 | g0214 | EUR | FIN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | FIN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0094 | EUR | FIN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00423 | hp1 | a0004 | c0010 | t0093 | g0147 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0149 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00438 | hp2 | a0001 | c0001 | t0086 | g0026 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00544 | hp1 | a0001 | c0001 | t0091 | g0137 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00544 | hp2 | a0001 | c0001 | t0050 | g0126 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00597 | hp2 | a0001 | c0001 | t0039 | g0118 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00621 | hp1 | a0001 | c0001 | t0014 | g0119 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0109 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00673 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | CHS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00735 | hp1 | a0001 | c0001 | t0024 | g0220 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0269 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG00741 | hp2 | a0001 | c0001 | t0018 | g0210 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01069 | hp1 | a0001 | c0011 | t0080 | g0227 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01074 | hp1 | a0001 | c0001 | t0083 | g0166 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01074 | hp2 | a0001 | c0001 | t0038 | g0142 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0057 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01109 | hp2 | a0001 | c0001 | t0077 | g0093 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01167 | hp2 | a0001 | c0001 | t0041 | g0222 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01169 | hp2 | a0001 | c0001 | t0057 | g0129 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01175 | hp1 | a0001 | c0001 | t0079 | g0266 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0218 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01255 | hp2 | a0001 | c0001 | t0075 | g0040 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01256 | hp1 | a0001 | c0001 | t0084 | g0099 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01256 | hp2 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01258 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01258 | hp2 | a0002 | c0002 | t0007 | g0038 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01261 | hp1 | a0001 | c0001 | t0011 | g0257 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0073 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0177 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0104 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01433 | hp1 | a0001 | c0014 | t0070 | g0191 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0268 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01496 | hp1 | a0001 | c0001 | t0054 | g0066 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01496 | hp2 | a0001 | c0001 | t0096 | g0139 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01515 | hp1 | a0001 | c0001 | t0029 | g0274 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0080 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01516 | hp2 | a0001 | c0001 | t0023 | g0219 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01517 | hp1 | a0001 | c0001 | t0029 | g0276 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0072 | EUR | IBS | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0007 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0135 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01891 | hp1 | a0001 | c0001 | t0092 | g0105 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01891 | hp2 | a0001 | c0001 | t0027 | g0011 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01975 | hp1 | a0001 | c0001 | t0073 | g0140 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02015 | hp2 | a0001 | c0001 | t0033 | g0264 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02027 | hp2 | a0001 | c0001 | t0024 | g0194 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02055 | hp1 | a0001 | c0001 | t0047 | g0319 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02055 | hp2 | a0001 | c0001 | t0090 | g0106 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02071 | hp1 | a0001 | c0001 | t0016 | g0178 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0245 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02074 | hp2 | a0001 | c0001 | t0011 | g0091 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02083 | hp2 | a0001 | c0001 | t0040 | g0146 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02145 | hp2 | a0001 | c0001 | t0037 | g0008 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02148 | hp1 | a0001 | c0001 | t0007 | g0035 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | CDX | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0050 | EAS | CDX | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | CDX | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02257 | hp1 | a0001 | c0001 | t0033 | g0277 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0069 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02280 | hp1 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02280 | hp2 | a0001 | c0001 | t0071 | g0273 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02293 | hp1 | a0001 | c0001 | t0005 | g0199 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0320 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0196 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0033 | AMR | PEL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02451 | hp1 | a0001 | c0001 | t0017 | g0314 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02451 | hp2 | a0001 | c0001 | t0065 | g0206 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0278 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0236 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02615 | hp1 | a0001 | c0001 | t0019 | g0161 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02622 | hp2 | a0001 | c0001 | t0032 | g0312 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02630 | hp1 | a0001 | c0003 | t0066 | g0315 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02630 | hp2 | a0001 | c0001 | t0088 | g0311 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0208 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02698 | hp1 | a0001 | c0001 | t0024 | g0292 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02698 | hp2 | a0001 | c0001 | t0059 | g0288 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02717 | hp2 | a0001 | c0001 | t0013 | g0114 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02723 | hp1 | a0001 | c0001 | t0055 | g0254 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02723 | hp2 | a0005 | c0006 | t0023 | g0107 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02738 | hp2 | a0001 | c0001 | t0009 | g0051 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02809 | hp1 | a0001 | c0001 | t0031 | g0155 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02809 | hp2 | a0001 | c0001 | t0046 | g0021 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02818 | hp2 | a0001 | c0001 | t0100 | g0122 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02886 | hp1 | a0001 | c0001 | t0045 | g0012 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02886 | hp2 | a0001 | c0001 | t0068 | g0179 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02896 | hp1 | a0001 | c0001 | t0013 | g0019 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0240 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02897 | hp1 | a0001 | c0001 | t0012 | g0228 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02897 | hp2 | a0001 | c0001 | t0095 | g0211 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02922 | hp2 | a0001 | c0001 | t0043 | g0307 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02965 | hp1 | a0001 | c0001 | t0049 | g0009 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02965 | hp2 | a0001 | c0001 | t0048 | g0299 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02970 | hp1 | a0001 | c0001 | t0017 | g0207 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0014 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02976 | hp1 | a0001 | c0001 | t0081 | g0305 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02976 | hp2 | a0001 | c0001 | t0067 | g0316 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0047 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03041 | hp1 | a0001 | c0001 | t0013 | g0116 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03041 | hp2 | a0001 | c0001 | t0089 | g0018 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0303 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03098 | hp2 | a0001 | c0001 | t0037 | g0225 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0209 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03195 | hp2 | a0001 | c0001 | t0019 | g0154 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0067 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03209 | hp2 | a0001 | c0001 | t0097 | g0310 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03225 | hp1 | a0001 | c0001 | t0038 | g0318 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0285 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03453 | hp2 | a0001 | c0001 | t0053 | g0004 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03486 | hp1 | a0001 | c0001 | t0056 | g0117 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03486 | hp2 | a0001 | c0001 | t0034 | g0308 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03491 | hp2 | a0001 | c0001 | t0030 | g0204 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03492 | hp2 | a0001 | c0001 | t0030 | g0205 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0309 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03516 | hp2 | a0001 | c0001 | t0027 | g0010 | AFR | ESN | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03540 | hp1 | a0001 | c0001 | t0019 | g0173 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03540 | hp2 | a0001 | c0001 | t0031 | g0150 | AFR | GWD | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03579 | hp2 | a0001 | c0001 | t0064 | g0180 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03654 | hp2 | a0001 | c0001 | t0026 | g0077 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03669 | hp1 | a0001 | c0001 | t0102 | g0136 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03669 | hp2 | a0001 | c0001 | t0060 | g0096 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0078 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | PJL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03834 | hp1 | a0001 | c0001 | t0009 | g0171 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03927 | hp2 | a0001 | c0001 | t0078 | g0162 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03942 | hp1 | a0001 | c0001 | t0052 | g0158 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03942 | hp2 | a0001 | c0001 | t0051 | g0030 | SAS | BEB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG04199 | hp1 | a0001 | c0001 | t0020 | g0048 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG04199 | hp2 | a0001 | c0001 | t0009 | g0189 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0235 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG04204 | hp2 | a0006 | c0007 | t0016 | g0123 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG04228 | hp1 | a0001 | c0001 | t0009 | g0152 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | CHB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18747 | hp2 | a0001 | c0001 | t0007 | g0148 | EAS | CHB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18906 | hp1 | a0001 | c0001 | t0087 | g0313 | AFR | YRI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18906 | hp2 | a0001 | c0012 | t0008 | g0006 | AFR | YRI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18942 | hp2 | a0001 | c0001 | t0022 | g0056 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18946 | hp2 | a0001 | c0001 | t0015 | g0237 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18951 | hp1 | a0001 | c0001 | t0020 | g0244 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18952 | hp1 | a0001 | c0001 | t0028 | g0233 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18954 | hp1 | a0002 | c0002 | t0004 | g0181 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18954 | hp2 | a0001 | c0001 | t0101 | g0079 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18959 | hp1 | a0001 | c0001 | t0022 | g0088 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18959 | hp2 | a0001 | c0001 | t0006 | g0249 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18960 | hp2 | a0001 | c0001 | t0015 | g0261 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18961 | hp1 | a0003 | c0004 | t0058 | g0082 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18964 | hp1 | a0001 | c0001 | t0021 | g0282 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18973 | hp2 | a0001 | c0001 | t0014 | g0087 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18977 | hp2 | a0001 | c0001 | t0094 | g0102 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18979 | hp1 | a0001 | c0001 | t0035 | g0042 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18981 | hp1 | a0001 | c0001 | t0034 | g0198 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18988 | hp2 | a0001 | c0001 | t0036 | g0128 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18990 | hp1 | a0001 | c0009 | t0082 | g0279 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18994 | hp1 | a0001 | c0001 | t0016 | g0293 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18998 | hp1 | a0001 | c0001 | t0014 | g0248 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19002 | hp1 | a0001 | c0001 | t0014 | g0283 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19005 | hp1 | a0001 | c0001 | t0098 | g0061 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19007 | hp1 | a0001 | c0001 | t0036 | g0280 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19007 | hp2 | a0001 | c0001 | t0007 | g0029 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19009 | hp1 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0304 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19011 | hp1 | a0001 | c0001 | t0028 | g0098 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19011 | hp2 | a0001 | c0001 | t0021 | g0281 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19043 | hp1 | a0001 | c0001 | t0076 | g0013 | AFR | LWK | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19043 | hp2 | a0001 | c0001 | t0061 | g0256 | AFR | LWK | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19056 | hp2 | a0001 | c0001 | t0042 | g0084 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19057 | hp2 | a0001 | c0001 | t0022 | g0060 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19058 | hp2 | a0001 | c0001 | t0072 | g0153 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19062 | hp1 | a0001 | c0001 | t0099 | g0253 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19064 | hp1 | a0008 | c0005 | t0025 | g0037 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19065 | hp1 | a0001 | c0001 | t0025 | g0045 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19068 | hp2 | a0001 | c0001 | t0021 | g0291 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19077 | hp1 | a0001 | c0001 | t0025 | g0230 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19077 | hp2 | a0001 | c0001 | t0020 | g0159 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19080 | hp2 | a0007 | c0008 | t0005 | g0262 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19083 | hp1 | a0001 | c0001 | t0035 | g0175 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19083 | hp2 | a0001 | c0001 | t0015 | g0238 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19088 | hp1 | a0001 | c0001 | t0015 | g0243 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19240 | hp1 | a0001 | c0001 | t0032 | g0023 | AFR | YRI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ASW | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20129 | hp2 | a0001 | c0001 | t0012 | g0188 | AFR | ASW | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | TSI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0001 | EUR | TSI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0217 | EUR | TSI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0317 | EUR | TSI | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0125 | SAS | GIH | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20905 | hp2 | a0001 | c0001 | t0085 | g0183 | SAS | GIH | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG01123 | hp2 | a0001 | c0001 | t0062 | g0068 | AMR | CLM | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02486 | hp1 | a0001 | c0001 | t0018 | g0226 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02486 | hp2 | a0001 | c0003 | t0063 | g0081 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02559 | hp1 | a0001 | c0001 | t0018 | g0020 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | ACB | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03471 | hp1 | a0001 | c0001 | t0023 | g0003 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | MSL | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG06807 | hp1 | a0001 | c0013 | t0010 | g0063 | AFR | USA | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0186 | AFR | USA | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0130 | AFR | USA | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
NA20300 | hp2 | a0001 | c0001 | t0044 | g0115 | AFR | USA | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0069 | g0197 | REF | REF | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0074 | g0216 | REF | REF | HNF4A_chr20_44350699_44437845 | HNF4A | chr20 | 44350699 | 44437845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:44413724
|
C | T | 1 | a0002 | 7 | HG01175.hp2 HG01258.hp2 HG01346.hp2 others(4): Show |
missense_variant | MODERATE | c.350C>T | p.Thr117Ile | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/10 | 456/4645 | 350/1359 | 117/452 | chr20 | 44413724 | ||
chr20:44413769
|
C | A | 1 | a0008 | 1 | NA19064.hp1 | missense_variant | MODERATE | c.395C>A | p.Ala132Glu | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/10 | 501/4645 | 395/1359 | 132/452 | chr20 | 44413769 | ||
chr20:44414519
|
G | A | 1 | a0003 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.439G>A | p.Val147Ile | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/10 | 545/4645 | 439/1359 | 147/452 | chr20 | 44414519 | ||
chr20:44424032
|
A | G | 1 | a0004 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.841A>G | p.Ser281Gly | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/10 | 947/4645 | 841/1359 | 281/452 | chr20 | 44424032 | ||
chr20:44428359
|
C | T | 1 | a0007 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.1088C>T | p.Ala363Val | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/10 | 1194/4645 | 1088/1359 | 363/452 | chr20 | 44428359 | ||
chr20:44428398
|
T | C | 1 | a0007 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.1127T>C | p.Met376Thr | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/10 | 1233/4645 | 1127/1359 | 376/452 | chr20 | 44428398 | ||
chr20:44428456
|
G | A | 1 | a0005 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.1185G>A | p.Met395Ile | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/10 | 1291/4645 | 1185/1359 | 395/452 | chr20 | 44428456 | ||
chr20:44429549
|
C | T | 1 | a0006 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1243C>T | p.Pro415Ser | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1349/4645 | 1243/1359 | 415/452 | chr20 | 44429549 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:44406143
|
C | T | 1 | a0001c0014 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.135C>T | p.Ala45Ala | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/10 | 241/4645 | 135/1359 | 45/452 | chr20 | 44406143 | ||
chr20:44413767
|
T | C | 2 | a0001c0003a0003c0004 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
synonymous_variant | LOW | c.393T>C | p.Asn131Asn | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/10 | 499/4645 | 393/1359 | 131/452 | chr20 | 44413767 | ||
chr20:44414656
|
C | T | 1 | a0001c0013 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.576C>T | p.Asp192Asp | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/10 | 682/4645 | 576/1359 | 192/452 | chr20 | 44414656 | ||
chr20:44418511
|
A | G | 1 | a0001c0012 | 1 | NA18906.hp2 | splice_region_variant&synonymous_variant | LOW | c.669A>G | p.Leu223Leu | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/10 | 775/4645 | 669/1359 | 223/452 | chr20 | 44418511 | ||
chr20:44419794
|
C | T | 1 | a0001c0011 | 1 | HG01069.hp1 | synonymous_variant | LOW | c.744C>T | p.Asp248Asp | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/10 | 850/4645 | 744/1359 | 248/452 | chr20 | 44419794 | ||
chr20:44424097
|
C | T | 1 | a0001c0009 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.906C>T | p.Asn302Asn | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/10 | 1012/4645 | 906/1359 | 302/452 | chr20 | 44424097 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:44355723
|
G | C | 2 | a0001c0001t0039a0001c0001t0040 | 2 | HG00597.hp2 HG02083.hp2 |
5_prime_UTR_variant | MODIFIER | c.-82G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/10 | 82 | chr20 | 44355723 | |||||
chr20:44429741
|
G | A | 1 | a0001c0001t0041 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 76 | chr20 | 44429741 | |||||
chr20:44429741
|
G | T | 1 | a0001c0001t0102 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 76 | chr20 | 44429741 | |||||
chr20:44429820
|
G | A | 5 | a0001c0001t0009a0001c0001t0016a0001c0001t0026others(2): Show | 11 | HG00280.hp1 HG02071.hp1 HG02738.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*155G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 155 | chr20 | 44429820 | |||||
chr20:44429832
|
T | A | 1 | a0001c0001t0043 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*167T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 167 | chr20 | 44429832 | |||||
chr20:44429907
|
T | C | 9 | a0001c0001t0017a0001c0001t0018a0001c0001t0027others(6): Show | 14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*242T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 242 | chr20 | 44429907 | |||||
chr20:44429942
|
T | A | 1 | a0001c0001t0050 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 277 | chr20 | 44429942 | |||||
chr20:44429942
|
T | C | 1 | a0001c0001t0051 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*277T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 277 | chr20 | 44429942 | |||||
chr20:44429970
|
A | G | 9 | a0001c0001t0017a0001c0001t0018a0001c0001t0027others(6): Show | 14 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*305A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 305 | chr20 | 44429970 | |||||
chr20:44430057
|
T | G | 23 | a0001c0001t0006a0001c0001t0017a0001c0001t0018others(20): Show | 38 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*392T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 392 | chr20 | 44430057 | |||||
chr20:44430058
|
G | A | 1 | a0001c0001t0062 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 393 | chr20 | 44430058 | |||||
chr20:44430092
|
G | T | 4 | a0001c0001t0015a0001c0001t0025a0001c0001t0101others(1): Show | 8 | NA18946.hp2 NA18954.hp2 NA18960.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*427G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 427 | chr20 | 44430092 | |||||
chr20:44430111
|
G | A | 1 | a0001c0001t0041 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*446G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 446 | chr20 | 44430111 | |||||
chr20:44430186
|
G | A | 2 | a0001c0001t0064a0001c0003t0063 | 2 | HG02486.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*521G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 521 | chr20 | 44430186 | |||||
chr20:44430233
|
G | A | 1 | a0001c0001t0065 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 568 | chr20 | 44430233 | |||||
chr20:44430322
|
G | A | 1 | a0001c0001t0019 | 3 | HG02615.hp1 HG03195.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*657G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 657 | chr20 | 44430322 | |||||
chr20:44430365
|
T | C | 4 | a0001c0001t0012a0001c0001t0067a0001c0001t0068others(1): Show | 7 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*700T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 700 | chr20 | 44430365 | |||||
chr20:44430450
|
G | A | 1 | a0001c0003t0063 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*785G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 785 | chr20 | 44430450 | |||||
chr20:44430571
|
A | C | 55 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(52): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*906A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 906 | chr20 | 44430571 | |||||
chr20:44430571
|
A | T | 9 | a0001c0001t0006a0001c0001t0029a0001c0001t0037others(6): Show | 20 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*906A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 906 | chr20 | 44430571 | |||||
chr20:44430572
|
G | A | 1 | a0001c0001t0083 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 907 | chr20 | 44430572 | |||||
chr20:44430597
|
TGAGGAAG others(12): Show |
T | 28 | a0001c0001t0003a0001c0001t0009a0001c0001t0014others(25): Show | 69 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*937_*955delAAGAAT others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 937 | INFO_REALIGN_3_PRIME | chr20 | 44430597 | ||||
chr20:44430636
|
GAGGGCCT others(104): Show |
G | 1 | a0001c0001t0083 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972_*1082del | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 972 | chr20 | 44430636 | |||||
chr20:44430642
|
C | G | 1 | a0003c0004t0058 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*977C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 977 | chr20 | 44430642 | |||||
chr20:44430733
|
C | T | 1 | a0001c0001t0045 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1068C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1068 | chr20 | 44430733 | |||||
chr20:44430743
|
G | A | 2 | a0001c0001t0084a0001c0001t0085 | 2 | HG01256.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1078G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1078 | chr20 | 44430743 | |||||
chr20:44430797
|
C | T | 53 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(50): Show | 142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*1132C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1132 | chr20 | 44430797 | |||||
chr20:44430955
|
ATCCTCCC others(1): Show |
A | 16 | a0001c0001t0015a0001c0001t0020a0001c0001t0026others(13): Show | 24 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1299_*1306delTCCT others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1299 | INFO_REALIGN_3_PRIME | chr20 | 44430955 | ||||
chr20:44431029
|
G | A | 1 | a0003c0004t0058 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1364G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1364 | chr20 | 44431029 | |||||
chr20:44431445
|
G | T | 1 | a0001c0001t0097 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1780G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1780 | chr20 | 44431445 | |||||
chr20:44431446
|
G | C | 1 | a0001c0001t0097 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1781G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1781 | chr20 | 44431446 | |||||
chr20:44431447
|
G | A | 1 | a0001c0001t0097 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1782G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1782 | chr20 | 44431447 | |||||
chr20:44431448
|
G | T | 1 | a0001c0001t0097 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1783G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1783 | chr20 | 44431448 | |||||
chr20:44431450
|
C | CTCTGTCT others(155): Show |
1 | a0001c0001t0097 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1786_*1787insCTGT others(158): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1787 | INFO_REALIGN_3_PRIME | chr20 | 44431450 | ||||
chr20:44431497
|
G | A | 7 | a0001c0001t0007a0001c0001t0014a0001c0001t0050others(4): Show | 16 | HG00544.hp2 HG00621.hp1 HG01255.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1832G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1832 | chr20 | 44431497 | |||||
chr20:44431640
|
G | A | 3 | a0001c0001t0010a0001c0001t0076a0001c0013t0010 | 6 | HG02145.hp1 HG02647.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1975G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 1975 | chr20 | 44431640 | |||||
chr20:44431847
|
G | A | 1 | a0001c0001t0021 | 3 | NA18964.hp1 NA19011.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2182G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2182 | chr20 | 44431847 | |||||
chr20:44432027
|
G | T | 1 | a0001c0001t0090 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2362G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2362 | chr20 | 44432027 | |||||
chr20:44432031
|
G | C | 17 | a0001c0001t0008a0001c0001t0010a0001c0001t0019others(14): Show | 31 | HG01109.hp2 HG01175.hp1 HG01256.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2366G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2366 | chr20 | 44432031 | |||||
chr20:44432107
|
A | T | 1 | a0004c0010t0093 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2442A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2442 | chr20 | 44432107 | |||||
chr20:44432198
|
G | A | 3 | a0001c0001t0017a0001c0001t0088a0001c0011t0080 | 5 | HG01069.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2533G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2533 | chr20 | 44432198 | |||||
chr20:44432321
|
G | A | 1 | a0001c0001t0095 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2656G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2656 | chr20 | 44432321 | |||||
chr20:44432344
|
C | CT | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*2703dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2704 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | ||||
chr20:44432344
|
C | CTT | 8 | a0001c0001t0011a0001c0001t0024a0001c0001t0034others(5): Show | 16 | HG00735.hp1 HG01261.hp1 HG02027.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2702_*2703dupTT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2704 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | ||||
chr20:44432344
|
CT | C | 11 | a0001c0001t0009a0001c0001t0019a0001c0001t0026others(8): Show | 19 | HG00280.hp1 HG01109.hp2 HG01496.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2703delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2703 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | ||||
chr20:44432344
|
CTTTTTTT | C | 5 | a0001c0001t0030a0001c0001t0032a0001c0001t0048others(2): Show | 7 | HG01975.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2697_*2703delTTTT others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2697 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | ||||
chr20:44432344
|
CTTTTTTT others(1): Show |
C | 4 | a0001c0001t0017a0001c0001t0081a0001c0001t0088others(1): Show | 6 | HG01069.hp1 HG02451.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2696_*2703delTTTT others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2696 | INFO_REALIGN_3_PRIME | chr20 | 44432344 | ||||
chr20:44432367
|
T | G | 2 | a0001c0001t0064a0001c0001t0067 | 2 | HG02976.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2702T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 2702 | chr20 | 44432367 | |||||
chr20:44432751
|
C | T | 1 | a0001c0001t0071 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3086C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 3086 | chr20 | 44432751 | |||||
chr20:44432803
|
CA | C | 2 | a0001c0001t0036a0001c0001t0099 | 3 | NA18988.hp2 NA19007.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3142delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 3142 | INFO_REALIGN_3_PRIME | chr20 | 44432803 | ||||
chr20:44432808
|
G | T | 2 | a0001c0001t0036a0001c0001t0099 | 3 | NA18988.hp2 NA19007.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3143G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 10/10 | 3143 | chr20 | 44432808 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr20:44355908
|
G | A | 2 | a0001c0001t0023g0003a0001c0001t0053g0004 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+55G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44355908 | ||||||
chr20:44355934
|
T | C | 1 | a0001c0001t0003g0005 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.49+81T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44355934 | ||||||
chr20:44356029
|
C | G | 1 | a0001c0001t0007g0320 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.49+176C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356029 | ||||||
chr20:44356264
|
C | A | 3 | a0001c0001t0008g0007a0001c0001t0037g0008a0001c0012t0008g0006 | 3 | HG01884.hp1 HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.49+411C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356264 | ||||||
chr20:44356275
|
G | A | 8 | a0001c0001t0010g0014a0001c0001t0010g0015a0001c0001t0010g0016others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+422G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356275 | ||||||
chr20:44356475
|
A | C | 2 | a0001c0001t0038g0318a0001c0001t0047g0319 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.49+622A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356475 | ||||||
chr20:44356615
|
A | C | 1 | a0001c0001t0001g0317 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49+762A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356615 | ||||||
chr20:44356616
|
C | T | 1 | a0001c0001t0067g0316 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+763C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356616 | ||||||
chr20:44356641
|
T | G | 2 | a0001c0001t0001g0017a0001c0001t0089g0018 | 2 | HG01361.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+788T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356641 | ||||||
chr20:44356715
|
A | G | 59 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(56): Show | 60 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.49+862A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356715 | ||||||
chr20:44356809
|
G | T | 4 | a0001c0001t0001g0255a0001c0001t0011g0257a0001c0001t0055g0254others(1): Show | 4 | HG01261.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+956G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356809 | ||||||
chr20:44356834
|
C | A | 5 | a0001c0001t0002g0022a0001c0001t0013g0019a0001c0001t0018g0020others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+981C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44356834 | ||||||
chr20:44357077
|
G | A | 82 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+1224G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44357077 | ||||||
chr20:44357398
|
A | G | 5 | a0001c0001t0002g0022a0001c0001t0013g0019a0001c0001t0018g0020others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+1545A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44357398 | ||||||
chr20:44357852
|
CACAA | C | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+2009_49+2012del others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44357852 | |||||
chr20:44358137
|
A | C | 1 | a0001c0001t0099g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.49+2284A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358137 | ||||||
chr20:44358143
|
C | A | 4 | a0001c0001t0004g0104a0001c0001t0090g0106a0001c0001t0092g0105others(1): Show | 4 | HG01361.hp1 HG01891.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+2290C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358143 | ||||||
chr20:44358144
|
A | T | 58 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(55): Show | 59 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+2291A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358144 | ||||||
chr20:44358248
|
GAA | G | 82 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+2408_49+2409del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358248 | |||||
chr20:44358259
|
A | AAAAAG | 47 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(44): Show | 48 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.49+2409_49+2410ins others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358259 | |||||
chr20:44358259
|
A | AAAAG | 10 | a0001c0001t0011g0309a0001c0001t0017g0314a0001c0001t0032g0312others(7): Show | 10 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+2410_49+2413dup others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358259 | |||||
chr20:44358408
|
G | A | 2 | a0001c0001t0013g0019a0001c0001t0018g0020 | 2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49+2555G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358408 | ||||||
chr20:44358470
|
T | C | 58 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(55): Show | 59 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.49+2617T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358470 | ||||||
chr20:44358490
|
A | G | 5 | a0001c0001t0002g0252a0001c0001t0003g0250a0001c0001t0004g0251others(2): Show | 5 | NA18941.hp1 NA18959.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+2637A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358490 | ||||||
chr20:44358496
|
G | C | 3 | a0001c0001t0001g0108a0001c0001t0006g0001a0001c0001t0006g0109 | 4 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+2643G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358496 | ||||||
chr20:44358619
|
CAAAA | C | 43 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(40): Show | 44 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.49+2767_49+2770del others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358619 | ||||||
chr20:44358620
|
A | C | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2767A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358620 | ||||||
chr20:44358620
|
A | G | 3 | a0001c0001t0001g0247a0001c0001t0038g0318a0001c0001t0047g0319 | 3 | HG02055.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+2767A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358620 | ||||||
chr20:44358622
|
AACAAAAC | A | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2771_49+2777del others(7): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358622 | |||||
chr20:44358623
|
A | C | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.49+2770A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358623 | ||||||
chr20:44358629
|
CAAA | C | 44 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(41): Show | 45 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.49+2781_49+2783del others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44358629 | |||||
chr20:44358632
|
A | T | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+2779A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358632 | ||||||
chr20:44358644
|
C | A | 1 | a0001c0001t0002g0024 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.49+2791C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358644 | ||||||
chr20:44358672
|
C | G | 9 | a0001c0001t0011g0309a0001c0001t0017g0314a0001c0001t0032g0312others(6): Show | 9 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+2819C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358672 | ||||||
chr20:44358755
|
C | T | 1 | a0001c0001t0032g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49+2902C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358755 | ||||||
chr20:44358869
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.49+3016T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358869 | ||||||
chr20:44358895
|
T | C | 63 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(60): Show | 64 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.49+3042T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358895 | ||||||
chr20:44358916
|
T | C | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+3063T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358916 | ||||||
chr20:44358929
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49+3076G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358929 | ||||||
chr20:44358967
|
G | A | 1 | a0001c0001t0002g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.49+3114G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44358967 | ||||||
chr20:44359113
|
T | A | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+3260T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359113 | ||||||
chr20:44359197
|
A | G | 1 | a0001c0001t0003g0246 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.49+3344A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359197 | ||||||
chr20:44359201
|
T | C | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+3348T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359201 | ||||||
chr20:44359237
|
G | C | 146 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(143): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.49+3384G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359237 | ||||||
chr20:44359398
|
CT | C | 9 | a0001c0001t0011g0309a0001c0001t0017g0314a0001c0001t0032g0312others(6): Show | 9 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+3549delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44359398 | |||||
chr20:44359432
|
C | T | 30 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0002g0229others(27): Show | 30 | HG01069.hp1 HG02071.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.49+3579C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359432 | ||||||
chr20:44359601
|
C | A | 1 | a0001c0001t0002g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.49+3748C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359601 | ||||||
chr20:44359663
|
G | A | 5 | a0001c0001t0002g0022a0001c0001t0013g0019a0001c0001t0018g0020others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+3810G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359663 | ||||||
chr20:44359677
|
C | T | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+3824C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44359677 | ||||||
chr20:44359809
|
TG | T | 82 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+3960delG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44359809 | |||||
chr20:44360062
|
C | T | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4209C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360062 | ||||||
chr20:44360183
|
G | A | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4330G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360183 | ||||||
chr20:44360201
|
A | G | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4348A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360201 | ||||||
chr20:44360391
|
G | A | 1 | a0001c0001t0013g0114 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+4538G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360391 | ||||||
chr20:44360549
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+4696G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360549 | ||||||
chr20:44360578
|
T | A | 4 | a0001c0001t0013g0116a0001c0001t0044g0115a0001c0001t0056g0117others(1): Show | 4 | HG02976.hp2 HG03041.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+4725T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360578 | ||||||
chr20:44360627
|
G | A | 82 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+4774G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360627 | ||||||
chr20:44360635
|
A | G | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4782A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360635 | ||||||
chr20:44360722
|
A | T | 2 | a0001c0001t0002g0022a0001c0001t0032g0023 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.49+4869A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360722 | ||||||
chr20:44360736
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+4883T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360736 | ||||||
chr20:44360841
|
G | C | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+4988G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44360841 | ||||||
chr20:44361032
|
C | T | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5179C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361032 | ||||||
chr20:44361050
|
A | G | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5197A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361050 | ||||||
chr20:44361074
|
T | C | 61 | a0001c0001t0001g0247a0001c0001t0001g0260a0001c0001t0001g0267others(58): Show | 62 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.49+5221T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361074 | ||||||
chr20:44361078
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.49+5225A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361078 | ||||||
chr20:44361137
|
G | A | 82 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+5284G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361137 | ||||||
chr20:44361154
|
C | A | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5301C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361154 | ||||||
chr20:44361329
|
T | A | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5476T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361329 | ||||||
chr20:44361576
|
A | C | 9 | a0001c0001t0011g0309a0001c0001t0017g0314a0001c0001t0032g0312others(6): Show | 9 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5723A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361576 | ||||||
chr20:44361655
|
C | T | 9 | a0001c0001t0011g0309a0001c0001t0017g0314a0001c0001t0032g0312others(6): Show | 9 | HG02451.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+5802C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361655 | ||||||
chr20:44361671
|
A | C | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+5818A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361671 | ||||||
chr20:44361692
|
A | C | 6 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0004g0297others(3): Show | 6 | HG00621.hp2 NA18946.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+5839A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361692 | ||||||
chr20:44361703
|
C | CAAAA | 6 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0004g0297others(3): Show | 6 | HG00621.hp2 NA18946.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+5850_49+5851ins others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361703 | ||||||
chr20:44361704
|
CA | C | 51 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(48): Show | 52 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.49+5860delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44361704 | |||||
chr20:44361705
|
A | C | 6 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0004g0297others(3): Show | 6 | HG00621.hp2 NA18946.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+5852A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44361705 | ||||||
chr20:44361717
|
C | CA | 51 | a0001c0001t0001g0247a0001c0001t0001g0260a0001c0001t0001g0267others(48): Show | 52 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.49+5872dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44361717 | |||||
chr20:44362000
|
C | G | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+6147C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362000 | ||||||
chr20:44362065
|
T | C | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+6212T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362065 | ||||||
chr20:44362075
|
C | G | 1 | a0001c0001t0024g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+6222C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362075 | ||||||
chr20:44362157
|
C | A | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+6304C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362157 | ||||||
chr20:44362190
|
C | T | 38 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0002g0229others(35): Show | 38 | HG01069.hp1 HG01891.hp2 HG02071.hp2 others(35): Show |
intron_variant | MODIFIER | c.49+6337C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362190 | ||||||
chr20:44362262
|
A | T | 2 | a0001c0001t0002g0022a0001c0001t0032g0023 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.49+6409A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362262 | ||||||
chr20:44362312
|
CG | C | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+6462delG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362312 | |||||
chr20:44362313
|
G | A | 94 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(91): Show | 94 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.49+6460G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362313 | ||||||
chr20:44362369
|
G | A | 122 | a0001c0001t0001g0017a0001c0001t0001g0108a0001c0001t0001g0110others(119): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.49+6516G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362369 | ||||||
chr20:44362371
|
G | C | 3 | a0001c0001t0017g0314a0001c0001t0087g0313a0001c0003t0066g0315 | 3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+6518G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362371 | ||||||
chr20:44362417
|
T | C | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+6564T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362417 | ||||||
chr20:44362418
|
T | TA | 11 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0201others(8): Show | 11 | HG00597.hp2 HG00621.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+6588dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362418 | |||||
chr20:44362418
|
TA | T | 49 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0239others(46): Show | 49 | HG00140.hp1 HG00438.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.49+6588delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362418 | |||||
chr20:44362418
|
TAA | T | 117 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(114): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.49+6587_49+6588del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362418 | |||||
chr20:44362418
|
TAAA | T | 6 | a0001c0001t0001g0290a0001c0001t0003g0112a0001c0001t0003g0259others(3): Show | 6 | HG00639.hp2 HG01167.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+6586_49+6588del others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362418 | |||||
chr20:44362634
|
G | C | 2 | a0001c0001t0004g0044a0001c0001t0025g0045 | 2 | HG00673.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.49+6781G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362634 | ||||||
chr20:44362646
|
C | CCATTTTA others(9): Show |
1 | a0001c0001t0034g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.49+6794_49+6809dup others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362646 | |||||
chr20:44362716
|
G | T | 1 | a0001c0001t0002g0252 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.49+6863G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362716 | ||||||
chr20:44362787
|
T | G | 52 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(49): Show | 53 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.49+6934T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362787 | ||||||
chr20:44362843
|
C | CT | 13 | a0001c0001t0001g0195a0001c0001t0001g0221a0001c0001t0002g0043others(10): Show | 13 | HG01256.hp1 HG01515.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.49+7006dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44362843 | |||||
chr20:44362848
|
T | TC | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+6995_49+6996ins others(1): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362848 | ||||||
chr20:44362864
|
C | T | 145 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(142): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.49+7011C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362864 | ||||||
chr20:44362867
|
A | G | 3 | a0001c0001t0017g0314a0001c0001t0087g0313a0001c0003t0066g0315 | 3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+7014A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362867 | ||||||
chr20:44362950
|
T | C | 3 | a0001c0001t0001g0124a0001c0001t0009g0125a0006c0007t0016g0123 | 3 | HG03239.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.49+7097T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362950 | ||||||
chr20:44362951
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0009g0125a0006c0007t0016g0123 | 3 | HG03239.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.49+7098C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44362951 | ||||||
chr20:44363020
|
AT | A | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+7176delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44363020 | |||||
chr20:44363027
|
T | G | 3 | a0001c0001t0017g0314a0001c0001t0087g0313a0001c0003t0066g0315 | 3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+7174T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363027 | ||||||
chr20:44363119
|
G | A | 3 | a0001c0001t0001g0247a0001c0001t0038g0318a0001c0001t0047g0319 | 3 | HG02055.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+7266G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363119 | ||||||
chr20:44363159
|
C | T | 49 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(46): Show | 50 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+7306C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363159 | ||||||
chr20:44363305
|
G | A | 1 | a0001c0001t0050g0126 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.49+7452G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363305 | ||||||
chr20:44363706
|
C | CT | 14 | a0001c0001t0001g0221a0001c0001t0002g0192a0001c0001t0002g0193others(11): Show | 14 | HG01167.hp2 HG01433.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+7875dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44363706 | |||||
chr20:44363706
|
CT | C | 128 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(125): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.49+7875delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44363706 | |||||
chr20:44363706
|
CTT | C | 12 | a0001c0001t0001g0290a0001c0001t0004g0046a0001c0001t0004g0258others(9): Show | 12 | HG01167.hp1 HG01256.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.49+7874_49+7875del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44363706 | |||||
chr20:44363719
|
T | C | 1 | a0001c0001t0055g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+7866T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363719 | ||||||
chr20:44363839
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+7986C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363839 | ||||||
chr20:44363991
|
C | T | 1 | a0001c0001t0001g0190 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.49+8138C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44363991 | ||||||
chr20:44364113
|
G | T | 1 | a0001c0001t0034g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.49+8260G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364113 | ||||||
chr20:44364253
|
G | T | 50 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(47): Show | 51 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.49+8400G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364253 | ||||||
chr20:44364289
|
G | C | 1 | a0001c0001t0079g0266 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.49+8436G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364289 | ||||||
chr20:44364307
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.49+8454C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364307 | ||||||
chr20:44364412
|
A | G | 1 | a0001c0001t0005g0047 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.49+8559A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364412 | ||||||
chr20:44364466
|
AT | A | 53 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(50): Show | 54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+8623delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44364466 | |||||
chr20:44364470
|
T | A | 1 | a0001c0001t0046g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+8617T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364470 | ||||||
chr20:44364474
|
T | C | 86 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(83): Show | 86 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.49+8621T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364474 | ||||||
chr20:44364507
|
G | C | 3 | a0001c0001t0017g0314a0001c0001t0087g0313a0001c0003t0066g0315 | 3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+8654G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364507 | ||||||
chr20:44364517
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+8664C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364517 | ||||||
chr20:44364533
|
C | T | 53 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(50): Show | 54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+8680C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364533 | ||||||
chr20:44364557
|
G | A | 4 | a0001c0001t0007g0130a0001c0001t0057g0129a0001c0014t0070g0191others(1): Show | 4 | HG01169.hp2 HG01175.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+8704G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364557 | ||||||
chr20:44364641
|
T | C | 1 | a0001c0001t0006g0278 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.49+8788T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364641 | ||||||
chr20:44364688
|
T | C | 50 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(47): Show | 51 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.49+8835T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364688 | ||||||
chr20:44364718
|
C | T | 53 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(50): Show | 54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+8865C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364718 | ||||||
chr20:44364944
|
C | A | 1 | a0001c0001t0034g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.49+9091C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44364944 | ||||||
chr20:44365035
|
G | A | 1 | a0001c0001t0013g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.49+9182G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365035 | ||||||
chr20:44365173
|
G | T | 4 | a0001c0001t0010g0208a0001c0001t0017g0207a0001c0001t0017g0209others(1): Show | 4 | HG00741.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+9320G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365173 | ||||||
chr20:44365314
|
G | T | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+9461G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365314 | ||||||
chr20:44365476
|
A | AT | 53 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(50): Show | 54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+9629dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44365476 | |||||
chr20:44365585
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+9732C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365585 | ||||||
chr20:44365692
|
C | T | 1 | a0001c0001t0009g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.49+9839C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365692 | ||||||
chr20:44365704
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.49+9851G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365704 | ||||||
chr20:44365728
|
C | T | 3 | a0001c0001t0017g0314a0001c0001t0087g0313a0001c0003t0066g0315 | 3 | HG02451.hp1 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+9875C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365728 | ||||||
chr20:44365729
|
G | A | 3 | a0001c0001t0010g0208a0001c0001t0017g0207a0001c0001t0017g0209 | 3 | HG02647.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.49+9876G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365729 | ||||||
chr20:44365733
|
G | A | 3 | a0001c0001t0001g0247a0001c0001t0038g0318a0001c0001t0047g0319 | 3 | HG02055.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+9880G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365733 | ||||||
chr20:44365749
|
G | A | 53 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(50): Show | 54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+9896G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365749 | ||||||
chr20:44365905
|
G | A | 53 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(50): Show | 54 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.49+10052G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365905 | ||||||
chr20:44365956
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0015g0261 | 2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.49+10103G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365956 | ||||||
chr20:44365990
|
C | G | 47 | a0001c0001t0001g0260a0001c0001t0001g0267a0001c0001t0001g0272others(44): Show | 48 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.49+10137C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44365990 | ||||||
chr20:44366022
|
C | T | 1 | a0001c0001t0015g0243 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.49+10169C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366022 | ||||||
chr20:44366086
|
GA | G | 3 | a0001c0001t0011g0186a0001c0001t0012g0187a0001c0001t0012g0188 | 3 | HG02280.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.49+10238delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44366086 | |||||
chr20:44366172
|
T | C | 76 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(73): Show | 76 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.49+10319T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366172 | ||||||
chr20:44366280
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.49+10427A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366280 | ||||||
chr20:44366343
|
G | A | 5 | a0001c0001t0011g0309a0001c0001t0032g0312a0001c0001t0034g0308others(2): Show | 5 | HG02622.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+10490G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366343 | ||||||
chr20:44366364
|
TA | T | 6 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+10513delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44366364 | |||||
chr20:44366387
|
A | G | 6 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+10534A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366387 | ||||||
chr20:44366490
|
A | G | 120 | a0001c0001t0001g0108a0001c0001t0001g0185a0001c0001t0001g0221others(117): Show | 122 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.49+10637A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366490 | ||||||
chr20:44366493
|
C | T | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+10640C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366493 | ||||||
chr20:44366552
|
T | G | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+10699T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366552 | ||||||
chr20:44366558
|
T | C | 1 | a0001c0001t0099g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.49+10705T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366558 | ||||||
chr20:44366563
|
G | A | 1 | a0001c0001t0002g0133 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.49+10710G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366563 | ||||||
chr20:44366730
|
T | C | 1 | a0001c0003t0066g0315 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49+10877T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366730 | ||||||
chr20:44366919
|
A | G | 1 | a0001c0001t0085g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.49+11066A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366919 | ||||||
chr20:44366960
|
G | A | 73 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(70): Show | 73 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49+11107G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366960 | ||||||
chr20:44366994
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.49+11141A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44366994 | ||||||
chr20:44367019
|
G | T | 1 | a0001c0001t0007g0320 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.49+11166G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367019 | ||||||
chr20:44367025
|
C | T | 9 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(6): Show | 9 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+11172C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367025 | ||||||
chr20:44367304
|
C | T | 5 | a0001c0001t0011g0309a0001c0001t0032g0312a0001c0001t0034g0308others(2): Show | 5 | HG02622.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+11451C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367304 | ||||||
chr20:44367335
|
CA | C | 14 | a0001c0001t0001g0290a0001c0001t0003g0112a0001c0001t0003g0259others(11): Show | 14 | HG00639.hp2 HG01167.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+11500delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44367335 | |||||
chr20:44367419
|
A | G | 123 | a0001c0001t0001g0108a0001c0001t0001g0185a0001c0001t0001g0221others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.49+11566A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367419 | ||||||
chr20:44367447
|
C | T | 111 | a0001c0001t0001g0108a0001c0001t0001g0185a0001c0001t0001g0221others(108): Show | 113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.49+11594C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367447 | ||||||
chr20:44367470
|
G | C | 73 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(70): Show | 73 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49+11617G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367470 | ||||||
chr20:44367544
|
G | C | 73 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(70): Show | 73 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49+11691G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367544 | ||||||
chr20:44367639
|
C | CA | 110 | a0001c0001t0001g0108a0001c0001t0001g0185a0001c0001t0001g0221others(107): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.49+11802dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44367639 | |||||
chr20:44367639
|
C | CAA | 9 | a0001c0001t0002g0022a0001c0001t0002g0229a0001c0001t0003g0112others(6): Show | 9 | HG00639.hp2 HG02615.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+11801_49+11802d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44367639 | |||||
chr20:44367681
|
C | T | 9 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(6): Show | 9 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+11828C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367681 | ||||||
chr20:44367797
|
C | A | 3 | a0001c0001t0001g0221a0001c0001t0017g0314a0001c0001t0087g0313 | 3 | HG02451.hp1 HG02922.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+11944C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44367797 | ||||||
chr20:44368053
|
CT | C | 8 | a0001c0001t0001g0255a0001c0001t0001g0302a0001c0001t0002g0303others(5): Show | 8 | HG02572.hp2 HG02818.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+12211delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368053 | |||||
chr20:44368073
|
A | AAT | 4 | a0001c0001t0001g0302a0001c0001t0003g0301a0001c0001t0004g0300others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+12233_49+12234d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368073 | |||||
chr20:44368084
|
ATATG | A | 4 | a0001c0001t0010g0208a0001c0001t0017g0207a0001c0001t0017g0209others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12233_49+12236d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368084 | |||||
chr20:44368086
|
A | ATG | 60 | a0001c0001t0001g0103a0001c0001t0001g0108a0001c0001t0001g0185others(57): Show | 61 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.49+12257_49+12258d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | |||||
chr20:44368086
|
A | ATGTG | 42 | a0001c0001t0001g0260a0001c0001t0001g0272a0001c0001t0001g0286others(39): Show | 43 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.49+12255_49+12258d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | |||||
chr20:44368086
|
A | ATGTGTG | 3 | a0001c0001t0003g0265a0001c0001t0004g0284a0001c0001t0059g0288 | 3 | HG02135.hp1 HG02698.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.49+12253_49+12258d others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | |||||
chr20:44368086
|
A | G | 5 | a0001c0001t0003g0217a0001c0001t0006g0218a0001c0001t0023g0219others(2): Show | 5 | HG00735.hp1 HG01255.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+12233A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368086 | ||||||
chr20:44368086
|
ATG | A | 12 | a0001c0001t0001g0221a0001c0001t0001g0247a0001c0001t0003g0005others(9): Show | 12 | HG00099.hp1 HG01261.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+12257_49+12258d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | |||||
chr20:44368086
|
ATGTG | A | 3 | a0001c0001t0013g0019a0001c0001t0018g0020a0001c0001t0046g0021 | 3 | HG02559.hp1 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.49+12255_49+12258d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368086 | |||||
chr20:44368134
|
G | GTATACAT others(9): Show |
2 | a0001c0001t0002g0303a0001c0001t0003g0301 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.49+12285_49+12286i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368134 | |||||
chr20:44368134
|
G | GTATACAT others(11): Show |
1 | a0001c0001t0048g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.49+12285_49+12286i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368134 | |||||
chr20:44368139
|
T | C | 6 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0010g0208others(3): Show | 6 | HG02630.hp1 HG02647.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+12286T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368139 | ||||||
chr20:44368141
|
C | CAT | 10 | a0001c0001t0001g0120a0001c0001t0001g0141a0001c0001t0001g0182others(7): Show | 10 | HG00544.hp1 HG01074.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.49+12307_49+12308d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368141 | |||||
chr20:44368141
|
C | CATAT | 14 | a0001c0001t0001g0170a0001c0001t0001g0195a0001c0001t0002g0169others(11): Show | 14 | HG01074.hp1 HG01123.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+12305_49+12308d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368141 | |||||
chr20:44368141
|
C | T | 10 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(7): Show | 10 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+12288C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368141 | ||||||
chr20:44368158
|
A | ATTTTTTT others(3): Show |
1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.49+12306_49+12307i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368158 | |||||
chr20:44368158
|
A | ATTTTTTT others(4): Show |
3 | a0001c0001t0004g0046a0001c0001t0004g0085a0001c0001t0004g0086 | 3 | NA18947.hp1 NA18981.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.49+12306_49+12307i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368158 | |||||
chr20:44368158
|
A | ATTTTTTT others(5): Show |
2 | a0001c0001t0014g0087a0001c0001t0075g0040 | 2 | HG01255.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.49+12306_49+12307i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368158 | |||||
chr20:44368160
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0025g0230 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0003g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0003g0231 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(30): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0003g0232 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(31): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0003g0246 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(30): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(17): Show |
1 | a0001c0011t0080g0227 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(26): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0018g0226 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(23): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0011g0309a0001c0001t0097g0310 | 2 | HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0252 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(28): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0037g0008a0001c0001t0037g0225 | 2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0034g0308a0001c0001t0088g0311 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(23): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(15): Show |
3 | a0001c0001t0006g0249a0001c0001t0014g0248a0001c0001t0015g0243 | 3 | NA18959.hp2 NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(16): Show |
4 | a0001c0001t0002g0097a0001c0001t0002g0234a0001c0001t0028g0233others(1): Show | 4 | HG02165.hp1 HG02622.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0003g0223a0001c0001t0003g0235 | 2 | HG04204.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(27): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0100g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0002g0229a0001c0001t0003g0250a0001c0001t0005g0236 | 3 | HG02602.hp2 NA18941.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0015g0237a0001c0001t0015g0238 | 2 | NA18946.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0239a0001c0001t0004g0251 | 2 | NA18961.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0241a0001c0001t0012g0228a0001c0001t0012g0240 | 3 | HG02647.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0020g0244 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(16): Show |
1 | a0002c0002t0001g0245 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(7): Show |
1 | a0001c0012t0008g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0108 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0185a0001c0001t0006g0109 | 2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0005g0269 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0270 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0017g0207 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(7): Show |
3 | a0001c0001t0006g0278a0001c0001t0038g0318a0001c0001t0081g0305 | 3 | HG02602.hp1 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0013g0184a0001c0001t0055g0254 | 2 | HG00099.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0006g0001a0001c0001t0008g0007a0001c0001t0011g0257others(1): Show | 5 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0267a0001c0001t0008g0268 | 2 | HG00642.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0017g0314a0001c0001t0027g0010a0001c0001t0027g0011others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(4): Show |
5 | a0001c0001t0005g0047a0001c0001t0010g0208a0001c0001t0017g0209others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0004g0258a0001c0001t0010g0014a0001c0001t0010g0015 | 3 | HG02145.hp1 HG02970.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0033g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0059g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0004g0304a0001c0001t0047g0319a0001c0009t0082g0279 | 3 | HG02055.hp1 NA18990.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0008g0002 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(11): Show |
4 | a0001c0001t0001g0272a0001c0001t0001g0286a0001c0001t0002g0271others(1): Show | 4 | HG00735.hp2 HG00741.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0024g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(3): Show |
3 | a0001c0001t0002g0022a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG02615.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(4): Show |
3 | a0001c0001t0005g0041a0001c0001t0010g0016a0001c0003t0066g0315 | 3 | HG02630.hp1 HG03139.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(5): Show |
5 | a0001c0001t0003g0027a0001c0001t0005g0049a0001c0001t0005g0050others(2): Show | 5 | HG02132.hp2 HG02155.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(6): Show |
2 | a0001c0001t0021g0281a0001c0001t0042g0084 | 2 | NA19011.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(7): Show |
10 | a0001c0001t0001g0260a0001c0001t0003g0094a0001c0001t0003g0095others(7): Show | 10 | HG00099.hp2 HG00323.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(8): Show |
3 | a0001c0001t0001g0247a0001c0001t0003g0265a0001c0001t0014g0283 | 3 | HG02135.hp1 HG03579.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(9): Show |
1 | a0001c0001t0003g0259 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.49+12308_49+12309i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(11): Show |
2 | a0001c0001t0003g0275a0001c0001t0029g0274 | 2 | HG01081.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATATTT others(12): Show |
2 | a0001c0001t0029g0276a0001c0001t0079g0266 | 2 | HG01175.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATTTTT others(3): Show |
3 | a0001c0001t0003g0028a0001c0001t0004g0052a0001c0001t0009g0051 | 3 | HG02015.hp1 HG02738.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATTTTT others(4): Show |
9 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0083others(6): Show | 9 | HG00423.hp2 HG00642.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATTTTT others(5): Show |
6 | a0001c0001t0001g0025a0001c0001t0003g0058a0001c0001t0003g0059others(3): Show | 6 | HG02148.hp2 HG03669.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATTTTT others(6): Show |
1 | a0001c0001t0022g0060 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.49+12308_49+12309i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATATTTTT others(7): Show |
3 | a0001c0001t0001g0287a0001c0001t0086g0026a0001c0001t0098g0061 | 3 | HG00438.hp2 HG03491.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.49+12308_49+12309i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0002g0031a0001c0013t0010g0063 | 2 | HG06807.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.49+12322_49+12331d others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATTTTTTT others(4): Show |
16 | a0001c0001t0001g0032a0001c0001t0001g0065a0001c0001t0001g0071others(13): Show | 16 | HG00140.hp1 HG01081.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.49+12321_49+12331d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATTTTTTT others(5): Show |
18 | a0001c0001t0001g0036a0001c0001t0001g0075a0001c0001t0001g0103others(15): Show | 18 | HG00597.hp1 HG00673.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.49+12320_49+12331d others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATTTTTTT others(6): Show |
3 | a0001c0001t0002g0039a0001c0001t0020g0048a0002c0002t0007g0038 | 3 | HG01258.hp2 HG01975.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.49+12319_49+12331d others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | ATTTTTTT others(7): Show |
1 | a0001c0003t0063g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49+12318_49+12331d others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44368160 | |||||
chr20:44368160
|
A | T | 6 | a0001c0001t0004g0046a0001c0001t0004g0085a0001c0001t0004g0086others(3): Show | 6 | HG01255.hp2 NA18947.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+12307A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368160 | ||||||
chr20:44368161
|
T | TA | 56 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0164others(53): Show | 56 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368161 | ||||||
chr20:44368161
|
T | TATA | 10 | a0001c0001t0002g0143a0001c0001t0002g0144a0001c0001t0002g0145others(7): Show | 10 | HG00597.hp2 HG00621.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+12308_49+12309i others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368161 | ||||||
chr20:44368162
|
T | A | 27 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0120others(24): Show | 27 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.49+12309T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368162 | ||||||
chr20:44368163
|
T | A | 51 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0164others(48): Show | 51 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.49+12310T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368163 | ||||||
chr20:44368164
|
T | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0141others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+12311T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368164 | ||||||
chr20:44368165
|
T | A | 2 | a0001c0001t0067g0316a0001c0001t0102g0136 | 2 | HG02976.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.49+12312T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368165 | ||||||
chr20:44368167
|
T | A | 1 | a0001c0001t0067g0316 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+12314T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368167 | ||||||
chr20:44368168
|
T | A | 2 | a0001c0001t0001g0255a0001c0001t0061g0256 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.49+12315T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368168 | ||||||
chr20:44368170
|
T | A | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+12317T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368170 | ||||||
chr20:44368334
|
T | C | 1 | a0001c0001t0047g0319 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49+12481T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368334 | ||||||
chr20:44368457
|
A | C | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+12604A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368457 | ||||||
chr20:44368457
|
A | G | 4 | a0001c0001t0010g0208a0001c0001t0017g0207a0001c0001t0017g0209others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12604A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368457 | ||||||
chr20:44368464
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.49+12611G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368464 | ||||||
chr20:44368593
|
G | T | 4 | a0001c0001t0010g0208a0001c0001t0017g0207a0001c0001t0017g0209others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+12740G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368593 | ||||||
chr20:44368709
|
T | A | 1 | a0001c0001t0044g0115 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.49+12856T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368709 | ||||||
chr20:44368739
|
A | G | 2 | a0001c0001t0003g0005a0001c0001t0003g0059 | 2 | NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.49+12886A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368739 | ||||||
chr20:44368800
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+12947T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368800 | ||||||
chr20:44368863
|
T | C | 4 | a0001c0001t0010g0208a0001c0001t0017g0207a0001c0001t0017g0209others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+13010T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368863 | ||||||
chr20:44368888
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49+13035G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368888 | ||||||
chr20:44368949
|
T | G | 4 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+13096T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368949 | ||||||
chr20:44368955
|
T | A | 9 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(6): Show | 9 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+13102T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368955 | ||||||
chr20:44368985
|
C | T | 2 | a0001c0001t0005g0072a0001c0001t0005g0080 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.49+13132C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44368985 | ||||||
chr20:44369072
|
CCT | C | 109 | a0001c0001t0001g0108a0001c0001t0001g0185a0001c0001t0001g0221others(106): Show | 111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.49+13220_49+13221d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369072 | ||||||
chr20:44369147
|
G | T | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.49+13294G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369147 | ||||||
chr20:44369188
|
T | G | 9 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(6): Show | 9 | HG02572.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+13335T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369188 | ||||||
chr20:44369249
|
C | CA | 92 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0120others(89): Show | 93 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.49+13425dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | |||||
chr20:44369249
|
C | CAA | 58 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(55): Show | 59 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.49+13424_49+13425d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | |||||
chr20:44369249
|
C | CAAA | 27 | a0001c0001t0001g0053a0001c0001t0001g0065a0001c0001t0001g0075others(24): Show | 27 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.49+13423_49+13425d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | |||||
chr20:44369249
|
C | CAAAA | 9 | a0001c0001t0004g0046a0001c0001t0004g0104a0001c0001t0006g0073others(6): Show | 9 | HG01069.hp1 HG01169.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+13422_49+13425d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | |||||
chr20:44369249
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0055g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49+13416_49+13425d others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | |||||
chr20:44369249
|
CA | C | 19 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0170others(16): Show | 19 | HG00735.hp1 HG01074.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.49+13425delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44369249 | |||||
chr20:44369279
|
C | T | 2 | a0001c0001t0013g0019a0001c0001t0018g0020 | 2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49+13426C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369279 | ||||||
chr20:44369286
|
G | A | 1 | a0001c0001t0003g0295 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.49+13433G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369286 | ||||||
chr20:44369631
|
G | A | 6 | a0001c0001t0004g0104a0001c0001t0033g0277a0001c0001t0081g0305others(3): Show | 6 | HG01361.hp1 HG01891.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+13778G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369631 | ||||||
chr20:44369707
|
T | C | 8 | a0001c0001t0001g0247a0001c0001t0001g0302a0001c0001t0002g0022others(5): Show | 8 | HG02572.hp2 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+13854T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369707 | ||||||
chr20:44369733
|
C | G | 1 | a0001c0001t0003g0095 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.49+13880C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369733 | ||||||
chr20:44369782
|
G | A | 3 | a0001c0001t0003g0005a0001c0001t0003g0059a0001c0001t0004g0054 | 3 | NA18951.hp2 NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.49+13929G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44369782 | ||||||
chr20:44370028
|
G | T | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+14175G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370028 | ||||||
chr20:44370082
|
G | A | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14229G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370082 | ||||||
chr20:44370089
|
C | G | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14236C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370089 | ||||||
chr20:44370089
|
C | T | 1 | a0001c0001t0003g0058 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.49+14236C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370089 | ||||||
chr20:44370090
|
G | A | 1 | a0001c0001t0032g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49+14237G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370090 | ||||||
chr20:44370096
|
G | C | 1 | a0001c0001t0006g0168 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.49+14243G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370096 | ||||||
chr20:44370112
|
C | T | 1 | a0001c0001t0059g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+14259C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370112 | ||||||
chr20:44370119
|
C | T | 6 | a0001c0001t0001g0247a0001c0001t0001g0302a0001c0001t0002g0303others(3): Show | 6 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.49+14266C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370119 | ||||||
chr20:44370121
|
G | A | 2 | a0001c0001t0003g0092a0001c0001t0024g0194 | 2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.49+14268G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370121 | ||||||
chr20:44370147
|
C | A | 1 | a0001c0001t0002g0169 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.49+14294C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370147 | ||||||
chr20:44370646
|
T | C | 3 | a0001c0001t0001g0141a0001c0001t0073g0140a0001c0001t0096g0139 | 3 | HG01496.hp2 HG01975.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.49+14793T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370646 | ||||||
chr20:44370691
|
A | G | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14838A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370691 | ||||||
chr20:44370697
|
C | T | 1 | a0001c0001t0007g0089 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.49+14844C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370697 | ||||||
chr20:44370714
|
C | T | 2 | a0001c0001t0001g0239a0002c0002t0001g0245 | 2 | HG02071.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.49+14861C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370714 | ||||||
chr20:44370715
|
G | A | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14862G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370715 | ||||||
chr20:44370793
|
G | A | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+14940G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370793 | ||||||
chr20:44370806
|
T | C | 3 | a0001c0001t0013g0019a0001c0001t0018g0020a0001c0001t0046g0021 | 3 | HG02559.hp1 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.49+14953T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370806 | ||||||
chr20:44370867
|
C | G | 1 | a0001c0001t0004g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.49+15014C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370867 | ||||||
chr20:44370893
|
C | A | 2 | a0001c0001t0017g0314a0001c0001t0087g0313 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.49+15040C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370893 | ||||||
chr20:44370990
|
A | C | 138 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.49+15137A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44370990 | ||||||
chr20:44371003
|
C | G | 259 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(256): Show | 260 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.49+15150C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371003 | ||||||
chr20:44371048
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+15195T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371048 | ||||||
chr20:44371199
|
A | C | 13 | a0001c0001t0001g0110a0001c0001t0001g0247a0001c0001t0001g0255others(10): Show | 13 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.49+15346A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371199 | ||||||
chr20:44371224
|
C | A | 7 | a0001c0001t0001g0110a0001c0001t0001g0255a0001c0001t0002g0022others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+15371C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371224 | ||||||
chr20:44371267
|
A | AT | 8 | a0001c0001t0001g0110a0001c0001t0001g0247a0001c0001t0001g0255others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+15422dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44371267 | |||||
chr20:44371363
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+15510C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371363 | ||||||
chr20:44371475
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.49+15622C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371475 | ||||||
chr20:44371553
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+15700G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371553 | ||||||
chr20:44371698
|
G | A | 8 | a0001c0001t0010g0014a0001c0001t0010g0015a0001c0001t0010g0016others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+15845G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371698 | ||||||
chr20:44371814
|
C | T | 8 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | HG01358.hp1 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+15961C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371814 | ||||||
chr20:44371817
|
T | A | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+15964T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371817 | ||||||
chr20:44371903
|
A | G | 1 | a0001c0001t0061g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49+16050A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371903 | ||||||
chr20:44371950
|
C | T | 111 | a0001c0001t0001g0017a0001c0001t0001g0121a0001c0001t0001g0124others(108): Show | 111 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.49+16097C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371950 | ||||||
chr20:44371982
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+16129C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44371982 | ||||||
chr20:44372123
|
C | A | 6 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(3): Show | 6 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+16270C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372123 | ||||||
chr20:44372340
|
C | T | 3 | a0001c0001t0007g0130a0001c0014t0070g0191a0002c0002t0001g0131 | 3 | HG01175.hp2 HG01433.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.49+16487C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372340 | ||||||
chr20:44372565
|
T | C | 2 | a0001c0001t0013g0019a0001c0001t0018g0020 | 2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49+16712T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372565 | ||||||
chr20:44372661
|
GT | G | 9 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(6): Show | 9 | HG02451.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+16817delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44372661 | |||||
chr20:44372666
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49+16813T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372666 | ||||||
chr20:44372812
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+16959G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372812 | ||||||
chr20:44372814
|
G | A | 1 | a0001c0001t0032g0023 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.49+16961G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372814 | ||||||
chr20:44372830
|
A | G | 2 | a0001c0001t0078g0162a0001c0001t0085g0183 | 2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.49+16977A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372830 | ||||||
chr20:44372843
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+16990C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44372843 | ||||||
chr20:44373081
|
C | T | 75 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(72): Show | 75 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.49+17228C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373081 | ||||||
chr20:44373192
|
C | T | 4 | a0001c0001t0017g0314a0001c0001t0031g0150a0001c0001t0031g0155others(1): Show | 4 | HG02451.hp1 HG02809.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+17339C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373192 | ||||||
chr20:44373503
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.49+17650C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373503 | ||||||
chr20:44373909
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0009g0125a0006c0007t0016g0123 | 3 | HG03239.hp2 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.49+18056C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373909 | ||||||
chr20:44373988
|
C | T | 1 | a0001c0001t0047g0319 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49+18135C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44373988 | ||||||
chr20:44374144
|
C | G | 1 | a0001c0001t0098g0061 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.49+18291C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374144 | ||||||
chr20:44374183
|
A | C | 14 | a0001c0001t0001g0110a0001c0001t0001g0255a0001c0001t0001g0302others(11): Show | 14 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+18330A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374183 | ||||||
chr20:44374185
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+18332C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374185 | ||||||
chr20:44374270
|
G | T | 259 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(256): Show | 260 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.49+18417G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374270 | ||||||
chr20:44374317
|
C | T | 8 | a0001c0001t0001g0255a0001c0001t0001g0302a0001c0001t0002g0303others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+18464C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374317 | ||||||
chr20:44374344
|
TGAACTTG others(99): Show |
T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18492_49+18597d others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374344 | ||||||
chr20:44374455
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18602A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374455 | ||||||
chr20:44374457
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18604G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374457 | ||||||
chr20:44374459
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18606C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374459 | ||||||
chr20:44374463
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18610C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374463 | ||||||
chr20:44374465
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18612A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374465 | ||||||
chr20:44374466
|
C | T | 10 | a0001c0001t0001g0247a0001c0001t0001g0255a0001c0001t0001g0302others(7): Show | 10 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.49+18613C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374466 | ||||||
chr20:44374468
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18615G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374468 | ||||||
chr20:44374473
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18620G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374473 | ||||||
chr20:44374478
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18625G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374478 | ||||||
chr20:44374482
|
G | A | 73 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(70): Show | 73 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49+18629G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374482 | ||||||
chr20:44374486
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18633T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374486 | ||||||
chr20:44374495
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18642A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374495 | ||||||
chr20:44374503
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18650A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374503 | ||||||
chr20:44374527
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18674A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374527 | ||||||
chr20:44374533
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18680A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374533 | ||||||
chr20:44374545
|
C | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18692C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374545 | ||||||
chr20:44374549
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18696T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374549 | ||||||
chr20:44374557
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18704A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374557 | ||||||
chr20:44374564
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18711A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374564 | ||||||
chr20:44374577
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18724T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374577 | ||||||
chr20:44374589
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18736A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374589 | ||||||
chr20:44374601
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18748T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374601 | ||||||
chr20:44374603
|
A | G | 7 | a0001c0001t0001g0110a0001c0001t0001g0255a0001c0001t0002g0022others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+18750A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374603 | ||||||
chr20:44374609
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18756A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374609 | ||||||
chr20:44374610
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18757T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374610 | ||||||
chr20:44374611
|
G | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18758G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374611 | ||||||
chr20:44374612
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18759T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374612 | ||||||
chr20:44374615
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18762C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374615 | ||||||
chr20:44374620
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18767T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374620 | ||||||
chr20:44374624
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49+18771T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374624 | ||||||
chr20:44374711
|
G | A | 1 | a0001c0001t0045g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.49+18858G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374711 | ||||||
chr20:44374744
|
G | A | 3 | a0001c0001t0010g0208a0001c0001t0017g0207a0001c0001t0017g0209 | 3 | HG02647.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.49+18891G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44374744 | ||||||
chr20:44375168
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+19315G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375168 | ||||||
chr20:44375178
|
C | A | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+19325C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375178 | ||||||
chr20:44375255
|
TTAAGTTC others(30): Show |
T | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.49+19417_49+19453d others(39): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44375255 | |||||
chr20:44375396
|
G | A | 2 | a0001c0001t0052g0158a0001c0001t0102g0136 | 2 | HG03669.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.49+19543G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375396 | ||||||
chr20:44375495
|
G | GT | 12 | a0001c0001t0001g0108a0001c0001t0001g0213a0001c0001t0001g0215others(9): Show | 12 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+19654dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44375495 | |||||
chr20:44375495
|
GT | G | 8 | a0001c0001t0001g0255a0001c0001t0001g0302a0001c0001t0002g0303others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+19654delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44375495 | |||||
chr20:44375598
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49+19745T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375598 | ||||||
chr20:44375986
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+20133C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44375986 | ||||||
chr20:44376084
|
A | G | 6 | a0001c0001t0011g0257a0001c0001t0013g0019a0001c0001t0017g0314others(3): Show | 6 | HG01261.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+20231A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376084 | ||||||
chr20:44376121
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.49+20268C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376121 | ||||||
chr20:44376126
|
A | G | 14 | a0001c0001t0001g0110a0001c0001t0001g0255a0001c0001t0001g0302others(11): Show | 14 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.49+20273A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376126 | ||||||
chr20:44376147
|
C | T | 6 | a0001c0001t0001g0110a0001c0001t0002g0022a0001c0001t0010g0208others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+20294C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376147 | ||||||
chr20:44376213
|
C | T | 1 | a0001c0001t0003g0235 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.49+20360C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376213 | ||||||
chr20:44376276
|
T | A | 1 | a0001c0001t0038g0142 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.49+20423T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376276 | ||||||
chr20:44376284
|
T | G | 1 | a0001c0001t0011g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.49+20431T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376284 | ||||||
chr20:44376375
|
A | G | 241 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(238): Show | 242 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.49+20522A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376375 | ||||||
chr20:44376385
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0002g0169 | 2 | HG03453.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.49+20532G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376385 | ||||||
chr20:44376489
|
A | G | 5 | a0001c0001t0011g0309a0001c0001t0032g0312a0001c0001t0034g0308others(2): Show | 5 | HG02622.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.49+20636A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376489 | ||||||
chr20:44376806
|
G | T | 1 | a0008c0005t0025g0037 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.49+20953G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376806 | ||||||
chr20:44376965
|
C | T | 2 | a0001c0001t0013g0019a0001c0001t0018g0020 | 2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49+21112C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44376965 | ||||||
chr20:44377194
|
C | G | 1 | a0001c0001t0038g0142 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.49+21341C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377194 | ||||||
chr20:44377205
|
T | C | 1 | a0001c0001t0009g0152 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.49+21352T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377205 | ||||||
chr20:44377292
|
A | G | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG01346.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.49+21439A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377292 | ||||||
chr20:44377335
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.49+21482C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377335 | ||||||
chr20:44377613
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+21760A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377613 | ||||||
chr20:44377681
|
T | TAAACCTG others(4): Show |
1 | a0001c0001t0009g0189 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.49+21829_49+21839d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44377681 | |||||
chr20:44377698
|
TAA | T | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+21852_49+21853d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44377698 | |||||
chr20:44377895
|
G | T | 1 | a0001c0001t0064g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.49+22042G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44377895 | ||||||
chr20:44378139
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+22286T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378139 | ||||||
chr20:44378198
|
A | G | 3 | a0001c0001t0001g0110a0001c0001t0002g0022a0001c0001t0032g0023 | 3 | HG02572.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.49+22345A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378198 | ||||||
chr20:44378226
|
T | C | 1 | a0001c0001t0046g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49+22373T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378226 | ||||||
chr20:44378271
|
A | AT | 76 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(73): Show | 76 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.49+22433dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378271 | |||||
chr20:44378271
|
AT | A | 9 | a0001c0001t0001g0110a0001c0001t0001g0255a0001c0001t0001g0260others(6): Show | 9 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.49+22433delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378271 | |||||
chr20:44378512
|
T | C | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+22659T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378512 | ||||||
chr20:44378627
|
T | G | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+22774T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378627 | ||||||
chr20:44378780
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.49+22927G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378780 | ||||||
chr20:44378789
|
C | T | 8 | a0001c0001t0001g0255a0001c0001t0001g0302a0001c0001t0002g0303others(5): Show | 8 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+22936C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378789 | ||||||
chr20:44378792
|
G | C | 49 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(46): Show | 50 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+22939G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378792 | ||||||
chr20:44378848
|
A | G | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+22995A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378848 | ||||||
chr20:44378918
|
C | CA | 6 | a0001c0001t0003g0263a0001c0001t0004g0104a0001c0001t0004g0304others(3): Show | 6 | HG01361.hp1 HG02055.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+23081dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378918 | |||||
chr20:44378918
|
CA | C | 81 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.49+23081delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378918 | |||||
chr20:44378918
|
CAA | C | 171 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0121others(168): Show | 171 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.49+23080_49+23081d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378918 | |||||
chr20:44378918
|
CAAA | C | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23079_49+23081d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44378918 | |||||
chr20:44378928
|
A | G | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23075A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378928 | ||||||
chr20:44378950
|
G | T | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+23097G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44378950 | ||||||
chr20:44379105
|
T | A | 44 | a0001c0001t0001g0017a0001c0001t0001g0141a0001c0001t0001g0157others(41): Show | 44 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.49+23252T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379105 | ||||||
chr20:44379105
|
T | C | 1 | a0001c0001t0059g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.49+23252T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379105 | ||||||
chr20:44379179
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+23326T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379179 | ||||||
chr20:44379219
|
G | C | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23366G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379219 | ||||||
chr20:44379251
|
T | C | 1 | a0001c0001t0003g0005 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.49+23398T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379251 | ||||||
chr20:44379367
|
C | T | 1 | a0001c0001t0033g0277 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.49+23514C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379367 | ||||||
chr20:44379428
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+23575G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379428 | ||||||
chr20:44379508
|
A | C | 1 | a0001c0001t0005g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.49+23655A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379508 | ||||||
chr20:44379545
|
T | C | 1 | a0001c0001t0010g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.49+23692T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379545 | ||||||
chr20:44379591
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+23738G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379591 | ||||||
chr20:44379698
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.49+23845T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379698 | ||||||
chr20:44379720
|
T | TTC | 9 | a0001c0001t0001g0247a0001c0001t0001g0255a0001c0001t0001g0302others(6): Show | 9 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.49+23868_49+23869i others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44379720 | |||||
chr20:44379728
|
TC | T | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23877delC | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44379728 | |||||
chr20:44379730
|
CT | C | 82 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(79): Show | 82 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.49+23898delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44379730 | |||||
chr20:44379730
|
CTT | C | 102 | a0001c0001t0001g0017a0001c0001t0001g0121a0001c0001t0001g0124others(99): Show | 102 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.49+23897_49+23898d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44379730 | |||||
chr20:44379734
|
T | G | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+23881T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379734 | ||||||
chr20:44379838
|
A | T | 1 | a0001c0001t0003g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.49+23985A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379838 | ||||||
chr20:44379918
|
G | A | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+24065G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379918 | ||||||
chr20:44379953
|
T | C | 8 | a0001c0001t0001g0255a0001c0001t0001g0302a0001c0001t0002g0303others(5): Show | 8 | HG00639.hp2 HG02572.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+24100T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379953 | ||||||
chr20:44379979
|
G | A | 1 | a0001c0001t0041g0222 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.49+24126G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379979 | ||||||
chr20:44379989
|
C | T | 2 | a0001c0001t0002g0270a0001c0001t0005g0269 | 2 | HG00140.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.49+24136C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44379989 | ||||||
chr20:44380269
|
G | A | 3 | a0001c0001t0003g0112a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG00639.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.49+24416G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380269 | ||||||
chr20:44380317
|
A | G | 1 | a0001c0001t0072g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.49+24464A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380317 | ||||||
chr20:44380341
|
C | T | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG01346.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.49+24488C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380341 | ||||||
chr20:44380361
|
C | T | 1 | a0001c0001t0028g0098 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.49+24508C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380361 | ||||||
chr20:44380500
|
C | T | 56 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(53): Show | 57 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.49+24647C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380500 | ||||||
chr20:44380515
|
A | T | 4 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.49+24662A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380515 | ||||||
chr20:44380519
|
C | T | 107 | a0001c0001t0001g0017a0001c0001t0001g0121a0001c0001t0001g0124others(104): Show | 107 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.49+24666C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380519 | ||||||
chr20:44380625
|
G | C | 1 | a0001c0001t0024g0292 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.49+24772G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44380625 | ||||||
chr20:44381044
|
C | CTTTGA | 254 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(251): Show | 255 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.50-25013_50-25009d others(7): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44381044 | |||||
chr20:44381060
|
A | G | 11 | a0001c0001t0001g0110a0001c0001t0001g0255a0001c0001t0001g0302others(8): Show | 11 | HG02572.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-24998A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381060 | ||||||
chr20:44381277
|
A | AG | 3 | a0001c0001t0001g0110a0001c0001t0001g0255a0001c0001t0032g0023 | 3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.50-24780dupG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44381277 | |||||
chr20:44381279
|
C | G | 1 | a0001c0001t0002g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-24779C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381279 | ||||||
chr20:44381279
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0255a0001c0001t0032g0023 | 3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.50-24779C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381279 | ||||||
chr20:44381279
|
CT | C | 233 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(230): Show | 234 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.50-24760delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44381279 | |||||
chr20:44381279
|
CTT | C | 9 | a0001c0001t0001g0247a0001c0001t0002g0039a0001c0001t0013g0114others(6): Show | 9 | HG01496.hp2 HG01975.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-24761_50-24760d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44381279 | |||||
chr20:44381424
|
G | T | 1 | a0001c0001t0009g0152 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.50-24634G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381424 | ||||||
chr20:44381490
|
G | A | 243 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(240): Show | 244 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.50-24568G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381490 | ||||||
chr20:44381661
|
C | G | 1 | a0001c0001t0047g0319 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50-24397C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381661 | ||||||
chr20:44381723
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.50-24335G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381723 | ||||||
chr20:44381907
|
G | A | 5 | a0001c0001t0002g0083a0001c0001t0003g0005a0001c0001t0003g0059others(2): Show | 5 | HG00423.hp2 HG02155.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-24151G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381907 | ||||||
chr20:44381994
|
C | T | 3 | a0001c0001t0010g0208a0001c0001t0017g0207a0001c0001t0017g0209 | 3 | HG02647.hp1 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.50-24064C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44381994 | ||||||
chr20:44382063
|
A | G | 1 | a0001c0001t0034g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.50-23995A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382063 | ||||||
chr20:44382177
|
C | G | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-23881C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382177 | ||||||
chr20:44382181
|
C | T | 1 | a0001c0001t0056g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-23877C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382181 | ||||||
chr20:44382185
|
A | G | 180 | a0001c0001t0001g0017a0001c0001t0001g0108a0001c0001t0001g0110others(177): Show | 181 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.50-23873A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382185 | ||||||
chr20:44382215
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-23843A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382215 | ||||||
chr20:44382245
|
C | CT | 122 | a0001c0001t0001g0017a0001c0001t0001g0108a0001c0001t0001g0110others(119): Show | 123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.50-23801dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44382245 | |||||
chr20:44382245
|
CTTTT | C | 7 | a0001c0001t0002g0229a0001c0001t0015g0237a0001c0001t0015g0238others(4): Show | 7 | NA18946.hp2 NA18952.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-23804_50-23801d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44382245 | |||||
chr20:44382249
|
T | C | 77 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(74): Show | 77 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.50-23809T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382249 | ||||||
chr20:44382281
|
C | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-23777C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382281 | ||||||
chr20:44382324
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0002g0022a0001c0001t0032g0023 | 3 | HG02572.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-23734C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382324 | ||||||
chr20:44382385
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.50-23673C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382385 | ||||||
chr20:44382396
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-23662G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382396 | ||||||
chr20:44382435
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.50-23623C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382435 | ||||||
chr20:44382450
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-23608C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382450 | ||||||
chr20:44382529
|
G | A | 16 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(13): Show | 17 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.50-23529G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382529 | ||||||
chr20:44382705
|
T | G | 3 | a0001c0001t0037g0008a0001c0001t0037g0225a0001c0001t0100g0122 | 3 | HG02145.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.50-23353T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382705 | ||||||
chr20:44382906
|
C | T | 2 | a0001c0001t0001g0260a0001c0001t0015g0261 | 2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.50-23152C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382906 | ||||||
chr20:44382923
|
C | T | 75 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(72): Show | 75 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-23135C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44382923 | ||||||
chr20:44383051
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0006g0057a0001c0001t0006g0073others(5): Show | 8 | HG01109.hp1 HG01123.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-23007C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383051 | ||||||
chr20:44383378
|
T | C | 6 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0006g0001others(3): Show | 7 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-22680T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383378 | ||||||
chr20:44383451
|
T | C | 2 | a0001c0001t0023g0003a0001c0001t0053g0004 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-22607T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383451 | ||||||
chr20:44383489
|
T | C | 6 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(3): Show | 6 | HG02572.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-22569T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383489 | ||||||
chr20:44383549
|
C | CT | 84 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(81): Show | 84 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.50-22491dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44383549 | |||||
chr20:44383549
|
CT | C | 10 | a0001c0001t0001g0182a0001c0001t0001g0195a0001c0001t0001g0215others(7): Show | 10 | HG00323.hp1 HG01433.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.50-22491delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44383549 | |||||
chr20:44383566
|
T | A | 1 | a0001c0001t0002g0234 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.50-22492T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383566 | ||||||
chr20:44383567
|
TA | T | 12 | a0001c0001t0001g0110a0001c0001t0001g0302a0001c0001t0002g0022others(9): Show | 12 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-22488delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44383567 | |||||
chr20:44383568
|
A | T | 129 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.50-22490A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383568 | ||||||
chr20:44383588
|
C | T | 1 | a0001c0001t0072g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-22470C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383588 | ||||||
chr20:44383589
|
T | C | 1 | a0001c0001t0072g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-22469T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383589 | ||||||
chr20:44383638
|
G | A | 75 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(72): Show | 75 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-22420G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383638 | ||||||
chr20:44383638
|
G | T | 6 | a0001c0001t0002g0229a0001c0001t0015g0237a0001c0001t0015g0238others(3): Show | 6 | NA18946.hp2 NA18952.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-22420G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383638 | ||||||
chr20:44383680
|
A | T | 258 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(255): Show | 259 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.50-22378A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383680 | ||||||
chr20:44383857
|
AT | A | 104 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(101): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.50-22191delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44383857 | |||||
chr20:44383862
|
TTTTTTAA others(5): Show |
T | 1 | a0001c0001t0016g0293 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.50-22195_50-22184d others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383862 | ||||||
chr20:44383914
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0038g0318 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.50-22144G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383914 | ||||||
chr20:44383918
|
T | C | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-22140T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44383918 | ||||||
chr20:44384011
|
C | T | 1 | a0001c0001t0016g0178 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.50-22047C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384011 | ||||||
chr20:44384103
|
G | A | 1 | a0001c0001t0003g0296 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.50-21955G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384103 | ||||||
chr20:44384133
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-21925G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384133 | ||||||
chr20:44384152
|
CT | C | 15 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(12): Show | 16 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-21905delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384152 | ||||||
chr20:44384153
|
T | C | 36 | a0001c0001t0001g0239a0001c0001t0002g0097a0001c0001t0002g0229others(33): Show | 36 | HG00639.hp2 HG02055.hp1 HG02071.hp2 others(33): Show |
intron_variant | MODIFIER | c.50-21905T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384153 | ||||||
chr20:44384159
|
CT | C | 83 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.50-21873delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | |||||
chr20:44384159
|
CTT | C | 44 | a0001c0001t0001g0221a0001c0001t0001g0239a0001c0001t0002g0229others(41): Show | 44 | HG00639.hp2 HG01169.hp2 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.50-21874_50-21873d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | |||||
chr20:44384159
|
CTTT | C | 7 | a0001c0001t0001g0255a0001c0001t0002g0097a0001c0001t0011g0257others(4): Show | 7 | HG01261.hp1 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-21875_50-21873d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | |||||
chr20:44384159
|
CTTTTTTT | C | 6 | a0001c0001t0004g0167a0001c0001t0024g0194a0001c0001t0035g0175others(3): Show | 6 | HG02027.hp2 HG02630.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-21879_50-21873d others(9): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | |||||
chr20:44384159
|
CTTTTTTT others(1): Show |
C | 99 | a0001c0001t0001g0017a0001c0001t0001g0121a0001c0001t0001g0124others(96): Show | 99 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.50-21880_50-21873d others(10): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | |||||
chr20:44384159
|
CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0170a0001c0001t0004g0172a0001c0001t0012g0187others(3): Show | 6 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-21881_50-21873d others(11): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384159 | |||||
chr20:44384185
|
T | A | 4 | a0001c0001t0002g0024a0001c0001t0007g0089a0001c0001t0022g0088others(1): Show | 4 | NA18612.hp2 NA18959.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-21873T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384185 | ||||||
chr20:44384298
|
CTGTTTCA others(11): Show |
C | 1 | a0001c0001t0002g0229 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.50-21758_50-21741d others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384298 | |||||
chr20:44384472
|
C | CA | 7 | a0001c0001t0002g0156a0001c0001t0004g0138a0001c0001t0006g0249others(4): Show | 7 | HG02074.hp1 HG03516.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.50-21579dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44384472 | |||||
chr20:44384574
|
C | T | 1 | a0001c0001t0020g0048 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.50-21484C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384574 | ||||||
chr20:44384668
|
G | A | 5 | a0001c0001t0002g0113a0001c0001t0003g0151a0001c0001t0005g0199others(2): Show | 5 | HG02083.hp2 HG02293.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-21390G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384668 | ||||||
chr20:44384698
|
T | A | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21360T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384698 | ||||||
chr20:44384701
|
T | C | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21357T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384701 | ||||||
chr20:44384709
|
G | A | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21349G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384709 | ||||||
chr20:44384710
|
A | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21348A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384710 | ||||||
chr20:44384711
|
A | C | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21347A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384711 | ||||||
chr20:44384714
|
A | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21344A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384714 | ||||||
chr20:44384715
|
A | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21343A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384715 | ||||||
chr20:44384766
|
A | G | 2 | a0001c0001t0013g0019a0001c0001t0018g0020 | 2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.50-21292A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384766 | ||||||
chr20:44384987
|
C | G | 1 | a0001c0001t0002g0031 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.50-21071C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44384987 | ||||||
chr20:44385004
|
G | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21054G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385004 | ||||||
chr20:44385005
|
T | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-21053T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385005 | ||||||
chr20:44385057
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-21000_50-20999i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385057 | |||||
chr20:44385057
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0065g0206 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.50-21000_50-20999i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385057 | |||||
chr20:44385057
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0052g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.50-21000_50-20999i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385057 | |||||
chr20:44385059
|
C | CT | 12 | a0001c0001t0001g0241a0001c0001t0001g0260a0001c0001t0007g0130others(9): Show | 12 | HG00735.hp1 HG01069.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-20971dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTT | 6 | a0001c0001t0011g0186a0001c0001t0011g0309a0001c0001t0032g0312others(3): Show | 6 | HG02622.hp2 HG02630.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-20974_50-20971d others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTT | 11 | a0001c0001t0001g0201a0001c0001t0001g0239a0001c0001t0003g0223others(8): Show | 11 | HG02818.hp2 HG02896.hp1 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-20976_50-20971d others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT | 14 | a0001c0001t0002g0097a0001c0001t0002g0242a0001c0001t0003g0235others(11): Show | 14 | HG02071.hp2 HG02145.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-20977_50-20971d others(9): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0002g0070a0001c0001t0005g0041 | 2 | HG04228.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.50-20980_50-20971d others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0247a0001c0001t0007g0033 | 2 | HG02300.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.50-20981_50-20971d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(5): Show |
28 | a0001c0001t0001g0032a0001c0001t0001g0110a0001c0001t0002g0031others(25): Show | 28 | HG00140.hp1 HG01169.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.50-20982_50-20971d others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(6): Show |
27 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0065others(24): Show | 27 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-20983_50-20971d others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0071a0001c0001t0001g0127a0001c0001t0002g0043others(5): Show | 8 | HG00597.hp1 HG01081.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-20984_50-20971d others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(8): Show |
11 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0157others(8): Show | 11 | HG00642.hp2 HG01361.hp2 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.50-20985_50-20971d others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(9): Show |
19 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0182others(16): Show | 19 | HG00741.hp2 HG01358.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.50-20986_50-20971d others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(10): Show |
15 | a0001c0001t0001g0141a0001c0001t0002g0022a0001c0001t0002g0306others(12): Show | 15 | HG00423.hp1 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.50-20987_50-20971d others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(11): Show |
13 | a0001c0001t0002g0144a0001c0001t0002g0145a0001c0001t0002g0192others(10): Show | 13 | HG00438.hp1 HG00544.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.50-20988_50-20971d others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(12): Show |
8 | a0001c0001t0001g0255a0001c0001t0002g0133a0001c0001t0002g0143others(5): Show | 8 | HG00597.hp2 HG02056.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.50-20989_50-20971d others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(13): Show |
8 | a0001c0001t0001g0124a0001c0001t0002g0024a0001c0001t0002g0193others(5): Show | 8 | HG02027.hp2 HG02280.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-20990_50-20971d others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(14): Show |
9 | a0001c0001t0001g0121a0001c0001t0001g0195a0001c0001t0004g0167others(6): Show | 9 | HG01074.hp1 HG01515.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.50-20991_50-20971d others(23): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(15): Show |
5 | a0001c0001t0001g0170a0001c0001t0009g0125a0001c0001t0009g0189others(2): Show | 5 | HG03491.hp2 HG03492.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-20992_50-20971d others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(16): Show |
4 | a0001c0001t0002g0200a0001c0001t0030g0205a0001c0001t0099g0253others(1): Show | 4 | HG01346.hp2 HG03492.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-20993_50-20971d others(25): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(17): Show |
3 | a0001c0001t0001g0202a0001c0001t0001g0272a0001c0001t0035g0175 | 3 | HG00735.hp2 NA19062.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.50-20994_50-20971d others(26): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0004g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.50-20995_50-20971d others(27): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0213 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.50-20997_50-20971d others(29): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(27): Show |
1 | a0001c0001t0001g0215 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.50-20971_50-20970i others(36): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0026g0214 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.50-20971_50-20970i others(37): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
C | T | 5 | a0001c0001t0013g0114a0001c0001t0023g0003a0001c0001t0052g0158others(2): Show | 5 | HG02451.hp2 HG02717.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-20999C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385059 | ||||||
chr20:44385059
|
CTTTTTT | C | 22 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(19): Show | 24 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.50-20976_50-20971d others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(6): Show | 9 | HG01167.hp2 HG02572.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.50-20979_50-20971d others(11): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385059
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.50-20981_50-20971d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44385059 | |||||
chr20:44385168
|
G | A | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-20890G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385168 | ||||||
chr20:44385228
|
T | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-20830T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385228 | ||||||
chr20:44385286
|
C | T | 28 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(25): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-20772C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385286 | ||||||
chr20:44385326
|
A | G | 112 | a0001c0001t0001g0017a0001c0001t0001g0121a0001c0001t0001g0124others(109): Show | 112 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.50-20732A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385326 | ||||||
chr20:44385511
|
C | A | 1 | a0001c0001t0034g0198 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.50-20547C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385511 | ||||||
chr20:44385573
|
A | C | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-20485A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385573 | ||||||
chr20:44385586
|
A | G | 73 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(70): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-20472A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385586 | ||||||
chr20:44385712
|
A | G | 73 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(70): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-20346A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385712 | ||||||
chr20:44385720
|
T | C | 1 | a0001c0001t0047g0319 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50-20338T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385720 | ||||||
chr20:44385721
|
G | A | 1 | a0001c0001t0047g0319 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50-20337G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385721 | ||||||
chr20:44385729
|
A | G | 1 | a0001c0001t0047g0319 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.50-20329A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385729 | ||||||
chr20:44385899
|
G | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0255a0001c0001t0013g0019others(1): Show | 4 | HG02559.hp1 HG02896.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-20159G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385899 | ||||||
chr20:44385912
|
T | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-20146T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385912 | ||||||
chr20:44385920
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-20138C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385920 | ||||||
chr20:44385985
|
G | A | 2 | a0001c0001t0001g0260a0001c0001t0015g0261 | 2 | NA18941.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.50-20073G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44385985 | ||||||
chr20:44386016
|
C | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-20042C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386016 | ||||||
chr20:44386031
|
T | TGTA | 111 | a0001c0001t0001g0017a0001c0001t0001g0121a0001c0001t0001g0124others(108): Show | 111 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.50-20027_50-20026i others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386031 | ||||||
chr20:44386085
|
G | T | 28 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(25): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-19973G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386085 | ||||||
chr20:44386086
|
A | T | 28 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(25): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-19972A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386086 | ||||||
chr20:44386127
|
A | C | 1 | a0001c0001t0002g0234 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.50-19931A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386127 | ||||||
chr20:44386128
|
G | A | 1 | a0001c0001t0002g0234 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.50-19930G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386128 | ||||||
chr20:44386130
|
C | G | 4 | a0001c0001t0002g0043a0001c0001t0002g0076a0001c0001t0002g0101others(1): Show | 4 | NA18948.hp2 NA18960.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-19928C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386130 | ||||||
chr20:44386152
|
C | T | 1 | a0001c0001t0003g0058 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.50-19906C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386152 | ||||||
chr20:44386159
|
A | AT | 22 | a0001c0001t0001g0121a0001c0001t0001g0201a0001c0001t0002g0024others(19): Show | 22 | HG00438.hp1 HG01255.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.50-19874dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44386159 | |||||
chr20:44386159
|
AT | A | 112 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.50-19874delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44386159 | |||||
chr20:44386159
|
ATT | A | 41 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0174others(38): Show | 43 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.50-19875_50-19874d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44386159 | |||||
chr20:44386220
|
T | G | 2 | a0001c0001t0011g0257a0001c0001t0055g0254 | 2 | HG01261.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.50-19838T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386220 | ||||||
chr20:44386282
|
C | T | 73 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(70): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-19776C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386282 | ||||||
chr20:44386325
|
G | A | 28 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(25): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-19733G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386325 | ||||||
chr20:44386326
|
C | G | 1 | a0001c0001t0003g0028 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.50-19732C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386326 | ||||||
chr20:44386355
|
C | A | 2 | a0001c0001t0013g0019a0001c0001t0018g0020 | 2 | HG02559.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.50-19703C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386355 | ||||||
chr20:44386400
|
C | T | 1 | a0001c0001t0072g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-19658C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386400 | ||||||
chr20:44386468
|
C | G | 73 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(70): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-19590C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386468 | ||||||
chr20:44386478
|
T | G | 1 | a0001c0001t0072g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-19580T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386478 | ||||||
chr20:44386641
|
A | G | 269 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(266): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.50-19417A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386641 | ||||||
chr20:44386641
|
A | T | 1 | a0001c0001t0002g0169 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.50-19417A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386641 | ||||||
chr20:44386916
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-19142C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44386916 | ||||||
chr20:44387012
|
T | G | 4 | a0001c0001t0001g0127a0001c0001t0001g0221a0001c0001t0011g0257others(1): Show | 4 | HG01261.hp1 HG02109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-19046T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387012 | ||||||
chr20:44387023
|
C | G | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-19035C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387023 | ||||||
chr20:44387025
|
A | G | 47 | a0001c0001t0001g0127a0001c0001t0001g0221a0001c0001t0001g0239others(44): Show | 47 | HG00639.hp2 HG01261.hp1 HG02055.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-19033A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387025 | ||||||
chr20:44387073
|
T | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-18985T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387073 | ||||||
chr20:44387114
|
C | A | 1 | a0001c0001t0003g0259 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.50-18944C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387114 | ||||||
chr20:44387231
|
C | T | 3 | a0001c0001t0001g0110a0001c0001t0002g0022a0001c0001t0032g0023 | 3 | HG02572.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-18827C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387231 | ||||||
chr20:44387237
|
G | A | 7 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0003g0301others(4): Show | 7 | HG02572.hp2 HG02717.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-18821G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387237 | ||||||
chr20:44387242
|
C | T | 3 | a0001c0001t0018g0020a0001c0001t0064g0180a0001c0001t0068g0179 | 3 | HG02559.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.50-18816C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387242 | ||||||
chr20:44387288
|
T | TA | 39 | a0001c0001t0001g0036a0001c0001t0001g0103a0001c0001t0001g0110others(36): Show | 39 | HG00597.hp1 HG00621.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-18745dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | |||||
chr20:44387288
|
TA | T | 27 | a0001c0001t0001g0032a0001c0001t0001g0201a0001c0001t0001g0290others(24): Show | 27 | HG00140.hp1 HG00597.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.50-18745delA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | |||||
chr20:44387288
|
TAAA | T | 23 | a0001c0001t0001g0108a0001c0001t0001g0174a0001c0001t0001g0185others(20): Show | 25 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.50-18747_50-18745d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | |||||
chr20:44387288
|
TAAAAAAA others(3): Show |
T | 35 | a0001c0001t0001g0239a0001c0001t0001g0247a0001c0001t0002g0097others(32): Show | 35 | HG00639.hp2 HG01433.hp1 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.50-18754_50-18745d others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | |||||
chr20:44387288
|
TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0002g0229a0001c0001t0100g0122 | 2 | HG02818.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.50-18755_50-18745d others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387288 | |||||
chr20:44387344
|
G | A | 2 | a0001c0001t0017g0314a0001c0001t0087g0313 | 2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.50-18714G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387344 | ||||||
chr20:44387395
|
G | A | 1 | a0001c0001t0046g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-18663G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387395 | ||||||
chr20:44387406
|
G | A | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-18652G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387406 | ||||||
chr20:44387645
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-18413T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387645 | ||||||
chr20:44387655
|
C | CG | 100 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0053others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.50-18391dupG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387655 | |||||
chr20:44387655
|
C | CGG | 51 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0141others(48): Show | 51 | HG00621.hp2 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.50-18392_50-18391d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387655 | |||||
chr20:44387655
|
C | CGGG | 26 | a0001c0001t0001g0108a0001c0001t0001g0157a0001c0001t0001g0174others(23): Show | 27 | HG00280.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.50-18393_50-18391d others(5): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387655 | |||||
chr20:44387655
|
CG | C | 18 | a0001c0001t0001g0221a0001c0001t0002g0101a0001c0001t0002g0111others(15): Show | 18 | HG01258.hp2 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.50-18391delG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387655 | |||||
chr20:44387658
|
G | C | 2 | a0001c0001t0001g0103a0001c0001t0018g0020 | 2 | HG02559.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.50-18400G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387658 | ||||||
chr20:44387658
|
G | GC | 6 | a0001c0001t0002g0132a0001c0001t0002g0144a0001c0001t0002g0145others(3): Show | 6 | HG00621.hp1 HG00673.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-18400_50-18399i others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387658 | ||||||
chr20:44387660
|
G | C | 1 | a0001c0001t0099g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.50-18398G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387660 | ||||||
chr20:44387661
|
G | T | 3 | a0001c0001t0003g0028a0001c0001t0005g0196a0001c0001t0069g0197 | 3 | HG02015.hp1 HG02300.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.50-18397G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387661 | ||||||
chr20:44387662
|
G | T | 1 | a0001c0001t0011g0069 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-18396G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387662 | ||||||
chr20:44387665
|
G | A | 2 | a0001c0001t0002g0229a0001c0001t0100g0122 | 2 | HG02818.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.50-18393G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387665 | ||||||
chr20:44387668
|
A | C | 1 | a0001c0001t0100g0122 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.50-18390A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387668 | ||||||
chr20:44387668
|
A | G | 5 | a0001c0001t0009g0171a0001c0001t0016g0293a0001c0001t0021g0282others(2): Show | 5 | HG03834.hp1 NA18964.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-18390A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387668 | ||||||
chr20:44387670
|
G | C | 1 | a0001c0001t0002g0229 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.50-18388G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387670 | ||||||
chr20:44387670
|
G | GGC | 3 | a0001c0001t0035g0042a0001c0001t0072g0153a0007c0008t0005g0262 | 3 | NA18979.hp1 NA19058.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.50-18388_50-18387i others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387670 | ||||||
chr20:44387671
|
C | CG | 44 | a0001c0001t0001g0036a0001c0001t0001g0127a0001c0001t0001g0170others(41): Show | 44 | HG00597.hp1 HG01069.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.50-18379dupG | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387671 | |||||
chr20:44387671
|
C | G | 4 | a0001c0001t0016g0293a0001c0001t0035g0042a0001c0001t0072g0153others(1): Show | 4 | NA18979.hp1 NA18994.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-18387C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387671 | ||||||
chr20:44387680
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.50-18378C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387680 | ||||||
chr20:44387680
|
C | T | 1 | a0005c0006t0023g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-18378C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387680 | ||||||
chr20:44387683
|
T | C | 75 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0053others(72): Show | 75 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.50-18375T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387683 | ||||||
chr20:44387689
|
G | C | 1 | a0001c0001t0059g0288 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.50-18369G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387689 | ||||||
chr20:44387721
|
T | TA | 17 | a0001c0001t0001g0127a0001c0001t0001g0195a0001c0001t0001g0247others(14): Show | 17 | HG01256.hp1 HG01261.hp1 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-18324dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387721 | |||||
chr20:44387721
|
T | TAA | 92 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0053others(89): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.50-18325_50-18324d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44387721 | |||||
chr20:44387735
|
G | A | 1 | a0001c0001t0101g0079 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.50-18323G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44387735 | ||||||
chr20:44388090
|
AT | A | 12 | a0001c0001t0001g0127a0001c0001t0001g0221a0001c0001t0001g0247others(9): Show | 12 | HG01261.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.50-17957delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388090 | |||||
chr20:44388102
|
A | T | 1 | a0001c0001t0005g0294 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.50-17956A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388102 | ||||||
chr20:44388111
|
C | CA | 169 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0121others(166): Show | 169 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.50-17946dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388111 | |||||
chr20:44388269
|
T | A | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-17789T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388269 | ||||||
chr20:44388273
|
T | G | 204 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0121others(201): Show | 204 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.50-17785T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388273 | ||||||
chr20:44388278
|
C | T | 203 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0121others(200): Show | 203 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.50-17780C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388278 | ||||||
chr20:44388360
|
C | T | 2 | a0001c0001t0003g0301a0005c0006t0023g0107 | 2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.50-17698C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388360 | ||||||
chr20:44388371
|
G | GCACCCCC others(9): Show |
1 | a0001c0001t0044g0115 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.50-17687_50-17686i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388371 | ||||||
chr20:44388372
|
A | AC | 25 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0127others(22): Show | 25 | HG00140.hp1 HG00438.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-17678dupC | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(2): Show |
20 | a0001c0001t0001g0110a0001c0001t0001g0163a0001c0001t0001g0215others(17): Show | 20 | HG00323.hp1 HG00735.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(11): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(3): Show |
20 | a0001c0001t0001g0164a0001c0001t0001g0213a0001c0001t0002g0055others(17): Show | 20 | HG00280.hp1 HG01358.hp1 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(4): Show |
16 | a0001c0001t0001g0239a0001c0001t0002g0193a0001c0001t0008g0134others(13): Show | 16 | HG02071.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(13): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(5): Show |
21 | a0001c0001t0001g0182a0001c0001t0002g0024a0001c0001t0002g0133others(18): Show | 21 | HG00544.hp2 HG00621.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(6): Show |
23 | a0001c0001t0001g0201a0001c0001t0001g0267a0001c0001t0002g0306others(20): Show | 23 | HG00438.hp1 HG00544.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(15): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(7): Show |
31 | a0001c0001t0001g0157a0001c0001t0001g0170a0001c0001t0001g0260others(28): Show | 31 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(16): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(8): Show |
16 | a0001c0001t0001g0121a0001c0001t0001g0317a0001c0001t0003g0074others(13): Show | 16 | HG00423.hp1 HG00597.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(9): Show |
8 | a0001c0001t0001g0124a0001c0001t0001g0141a0001c0001t0002g0234others(5): Show | 8 | HG02074.hp1 HG02074.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(10): Show |
5 | a0001c0001t0001g0202a0001c0001t0002g0022a0001c0001t0004g0160others(2): Show | 5 | HG02300.hp1 HG02615.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(11): Show |
2 | a0001c0001t0005g0199a0001c0001t0035g0175 | 2 | HG02293.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.50-17678_50-17677i others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(12): Show |
2 | a0001c0001t0085g0183a0001c0012t0008g0006 | 2 | NA18906.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.50-17678_50-17677i others(21): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(13): Show |
4 | a0001c0001t0001g0017a0001c0001t0002g0169a0001c0001t0004g0104others(1): Show | 4 | HG01361.hp1 HG01361.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-17678_50-17677i others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | ACCCCCCC others(9): Show |
1 | a0001c0001t0002g0156 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.50-17678_50-17677i others(18): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388372 | |||||
chr20:44388372
|
A | C | 1 | a0001c0001t0044g0115 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.50-17686A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388372 | ||||||
chr20:44388374
|
C | CCCCCCCC others(23): Show |
1 | a0001c0001t0036g0128 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.50-17678_50-17677i others(32): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388374 | |||||
chr20:44388380
|
C | CCCCCCCC others(10): Show |
1 | a0001c0001t0001g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.50-17678_50-17677i others(19): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388380 | ||||||
chr20:44388381
|
A | C | 217 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(214): Show | 217 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.50-17677A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388381 | ||||||
chr20:44388381
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0013g0019 | 2 | HG02896.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.50-17677A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388381 | ||||||
chr20:44388382
|
C | A | 1 | a0001c0001t0002g0242 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.50-17676C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388382 | ||||||
chr20:44388383
|
C | CCCCCCCC others(18): Show |
1 | a0001c0001t0002g0229 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.50-17672_50-17671i others(27): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44388383 | |||||
chr20:44388430
|
T | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-17628T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388430 | ||||||
chr20:44388431
|
G | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-17627G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388431 | ||||||
chr20:44388476
|
C | T | 26 | a0001c0001t0001g0239a0001c0001t0002g0097a0001c0001t0002g0193others(23): Show | 26 | HG02071.hp2 HG02145.hp2 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.50-17582C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388476 | ||||||
chr20:44388644
|
G | T | 5 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(2): Show | 5 | HG02717.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-17414G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388644 | ||||||
chr20:44388899
|
C | A | 1 | a0001c0001t0038g0142 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.50-17159C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388899 | ||||||
chr20:44388908
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0023g0003a0001c0001t0053g0004 | 3 | HG02922.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.50-17150C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44388908 | ||||||
chr20:44389018
|
C | A | 1 | a0001c0001t0009g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.50-17040C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389018 | ||||||
chr20:44389133
|
T | G | 1 | a0001c0001t0006g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.50-16925T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389133 | ||||||
chr20:44389186
|
C | G | 1 | a0001c0001t0013g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.50-16872C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389186 | ||||||
chr20:44389439
|
C | T | 3 | a0001c0001t0003g0094a0001c0001t0003g0095a0001c0001t0060g0096 | 3 | HG00099.hp2 HG00323.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.50-16619C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389439 | ||||||
chr20:44389616
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.50-16442T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389616 | ||||||
chr20:44389620
|
G | A | 62 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0053others(59): Show | 62 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.50-16438G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389620 | ||||||
chr20:44389737
|
G | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-16321G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389737 | ||||||
chr20:44389738
|
T | C | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-16320T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389738 | ||||||
chr20:44389904
|
G | C | 1 | a0001c0001t0028g0098 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.50-16154G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44389904 | ||||||
chr20:44390107
|
A | G | 1 | a0001c0001t0005g0041 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.50-15951A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390107 | ||||||
chr20:44390112
|
C | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15946C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390112 | ||||||
chr20:44390210
|
G | A | 1 | a0001c0001t0013g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.50-15848G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390210 | ||||||
chr20:44390299
|
A | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15759A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390299 | ||||||
chr20:44390517
|
T | A | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15541T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390517 | ||||||
chr20:44390518
|
T | C | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15540T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390518 | ||||||
chr20:44390520
|
A | C | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15538A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390520 | ||||||
chr20:44390521
|
G | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15537G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390521 | ||||||
chr20:44390522
|
G | A | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15536G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390522 | ||||||
chr20:44390526
|
T | C | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15532T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390526 | ||||||
chr20:44390527
|
A | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15531A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390527 | ||||||
chr20:44390528
|
A | C | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15530A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390528 | ||||||
chr20:44390529
|
C | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15529C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390529 | ||||||
chr20:44390531
|
C | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15527C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390531 | ||||||
chr20:44390538
|
G | T | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15520G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390538 | ||||||
chr20:44390634
|
A | G | 1 | a0001c0001t0004g0258 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.50-15424A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44390634 | ||||||
chr20:44391065
|
A | T | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-14993A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391065 | ||||||
chr20:44391066
|
A | G | 1 | a0001c0001t0003g0223 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.50-14992A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391066 | ||||||
chr20:44391069
|
A | G | 21 | a0001c0001t0001g0053a0001c0001t0001g0065a0001c0001t0001g0071others(18): Show | 21 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.50-14989A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391069 | ||||||
chr20:44391072
|
C | T | 1 | a0001c0001t0079g0266 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.50-14986C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391072 | ||||||
chr20:44391095
|
C | T | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-14963C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391095 | ||||||
chr20:44391167
|
G | T | 1 | a0001c0001t0002g0022 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-14891G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391167 | ||||||
chr20:44391183
|
T | C | 6 | a0001c0001t0004g0172a0001c0001t0008g0134a0001c0001t0008g0135others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-14875T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391183 | ||||||
chr20:44391231
|
C | G | 1 | a0001c0001t0038g0142 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.50-14827C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391231 | ||||||
chr20:44391407
|
G | T | 1 | a0001c0001t0001g0272 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.50-14651G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391407 | ||||||
chr20:44391463
|
A | G | 123 | a0001c0001t0001g0053a0001c0001t0001g0062a0001c0001t0001g0065others(120): Show | 125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.50-14595A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391463 | ||||||
chr20:44391510
|
T | C | 10 | a0001c0001t0001g0127a0001c0001t0001g0170a0001c0001t0001g0247others(7): Show | 10 | HG00639.hp2 HG01074.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.50-14548T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391510 | ||||||
chr20:44391519
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.50-14539G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391519 | ||||||
chr20:44391523
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.50-14535C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391523 | ||||||
chr20:44391837
|
A | G | 1 | a0001c0001t0013g0019 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.50-14221A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391837 | ||||||
chr20:44391928
|
C | T | 13 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(10): Show | 13 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-14130C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44391928 | ||||||
chr20:44392029
|
G | A | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-14029G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392029 | ||||||
chr20:44392061
|
T | G | 1 | a0001c0001t0006g0109 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.50-13997T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392061 | ||||||
chr20:44392196
|
T | G | 2 | a0001c0001t0001g0127a0001c0001t0038g0318 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.50-13862T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392196 | ||||||
chr20:44392215
|
C | G | 1 | a0001c0001t0007g0035 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.50-13843C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392215 | ||||||
chr20:44392229
|
T | C | 12 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(9): Show | 12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-13829T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392229 | ||||||
chr20:44392244
|
G | A | 1 | a0001c0001t0050g0126 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.50-13814G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392244 | ||||||
chr20:44392257
|
G | GT | 12 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(9): Show | 12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-13800dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44392257 | |||||
chr20:44392266
|
C | T | 1 | a0001c0001t0084g0099 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.50-13792C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392266 | ||||||
chr20:44392284
|
T | C | 4 | a0001c0001t0002g0043a0001c0001t0002g0076a0001c0001t0002g0101others(1): Show | 4 | NA18948.hp2 NA18960.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-13774T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392284 | ||||||
chr20:44392302
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0038g0318 | 2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.50-13756G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392302 | ||||||
chr20:44392417
|
C | T | 4 | a0001c0001t0002g0043a0001c0001t0002g0076a0001c0001t0002g0101others(1): Show | 4 | NA18948.hp2 NA18960.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-13641C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392417 | ||||||
chr20:44392574
|
G | A | 24 | a0001c0001t0001g0174a0001c0001t0001g0185a0001c0001t0001g0247others(21): Show | 25 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(22): Show |
intron_variant | MODIFIER | c.50-13484G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392574 | ||||||
chr20:44392583
|
A | G | 24 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0003g0285others(21): Show | 24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.50-13475A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392583 | ||||||
chr20:44392816
|
T | C | 276 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(273): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.50-13242T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392816 | ||||||
chr20:44392885
|
C | T | 2 | a0001c0001t0008g0002a0001c0001t0008g0268 | 3 | HG01256.hp2 HG01258.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.50-13173C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44392885 | ||||||
chr20:44393184
|
G | A | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-12874G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393184 | ||||||
chr20:44393188
|
C | G | 1 | a0001c0001t0081g0305 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.50-12870C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393188 | ||||||
chr20:44393395
|
G | A | 4 | a0001c0001t0002g0133a0001c0001t0003g0005a0001c0001t0005g0149others(1): Show | 4 | HG00438.hp1 NA18988.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-12663G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393395 | ||||||
chr20:44393469
|
T | G | 5 | a0001c0001t0004g0172a0001c0001t0008g0134a0001c0001t0008g0135others(2): Show | 5 | HG01261.hp1 HG01884.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-12589T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393469 | ||||||
chr20:44393482
|
T | C | 2 | a0001c0001t0084g0099a0001c0001t0085g0183 | 2 | HG01256.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.50-12576T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393482 | ||||||
chr20:44393503
|
A | G | 2 | a0001c0001t0002g0022a0001c0001t0032g0023 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-12555A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393503 | ||||||
chr20:44393570
|
G | C | 4 | a0001c0001t0006g0278a0001c0001t0013g0116a0001c0001t0044g0115others(1): Show | 4 | HG02602.hp1 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-12488G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393570 | ||||||
chr20:44393676
|
C | T | 1 | a0001c0001t0078g0162 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.50-12382C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393676 | ||||||
chr20:44393807
|
A | G | 2 | a0001c0001t0002g0022a0001c0001t0032g0023 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-12251A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393807 | ||||||
chr20:44393818
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.50-12240G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393818 | ||||||
chr20:44393892
|
T | A | 1 | a0001c0001t0051g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.50-12166T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44393892 | ||||||
chr20:44394227
|
A | G | 3 | a0001c0001t0008g0007a0001c0001t0008g0067a0001c0012t0008g0006 | 3 | HG01884.hp1 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.50-11831A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394227 | ||||||
chr20:44394233
|
C | T | 12 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(9): Show | 12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-11825C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394233 | ||||||
chr20:44394280
|
C | A | 12 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(9): Show | 12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-11778C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394280 | ||||||
chr20:44394289
|
C | T | 12 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(9): Show | 12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.50-11769C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394289 | ||||||
chr20:44394355
|
T | C | 4 | a0001c0001t0006g0278a0001c0001t0013g0116a0001c0001t0044g0115others(1): Show | 4 | HG02602.hp1 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-11703T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394355 | ||||||
chr20:44394749
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-11309G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394749 | ||||||
chr20:44394784
|
C | A | 1 | a0001c0001t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.50-11274C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394784 | ||||||
chr20:44394788
|
G | A | 1 | a0001c0001t0019g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.50-11270G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394788 | ||||||
chr20:44394941
|
G | C | 1 | a0001c0001t0001g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-11117G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394941 | ||||||
chr20:44394943
|
C | G | 6 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 6 | HG01358.hp1 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-11115C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44394943 | ||||||
chr20:44395072
|
A | G | 2 | a0001c0001t0002g0022a0001c0001t0032g0023 | 2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.50-10986A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395072 | ||||||
chr20:44395201
|
A | G | 122 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0053others(119): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.50-10857A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395201 | ||||||
chr20:44395229
|
G | T | 2 | a0001c0001t0001g0221a0001c0001t0003g0112 | 2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-10829G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395229 | ||||||
chr20:44395267
|
C | T | 3 | a0001c0001t0056g0117a0001c0001t0090g0106a0001c0001t0092g0105 | 3 | HG01891.hp1 HG02055.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.50-10791C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395267 | ||||||
chr20:44395353
|
G | T | 1 | a0001c0001t0001g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-10705G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395353 | ||||||
chr20:44395368
|
T | C | 123 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0121others(120): Show | 124 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.50-10690T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395368 | ||||||
chr20:44395403
|
G | T | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-10655G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395403 | ||||||
chr20:44395409
|
G | T | 115 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0053others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.50-10649G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395409 | ||||||
chr20:44395565
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.50-10493C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395565 | ||||||
chr20:44395622
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-10436A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395622 | ||||||
chr20:44395624
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-10434G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395624 | ||||||
chr20:44395626
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.50-10432A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44395626 | ||||||
chr20:44396117
|
G | C | 2 | a0001c0001t0012g0228a0001c0001t0012g0240 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.50-9941G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396117 | ||||||
chr20:44396147
|
G | A | 2 | a0001c0001t0031g0150a0001c0001t0031g0155 | 2 | HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.50-9911G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396147 | ||||||
chr20:44396148
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.50-9910G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396148 | ||||||
chr20:44396174
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0170a0001c0001t0083g0166 | 3 | HG01074.hp1 HG03492.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.50-9884G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396174 | ||||||
chr20:44396239
|
G | A | 1 | a0001c0001t0072g0153 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.50-9819G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396239 | ||||||
chr20:44396436
|
A | G | 2 | a0001c0001t0001g0221a0001c0001t0003g0112 | 2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9622A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396436 | ||||||
chr20:44396467
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0003g0112 | 2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9591G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396467 | ||||||
chr20:44396475
|
T | C | 1 | a0001c0001t0077g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.50-9583T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396475 | ||||||
chr20:44396708
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0003g0112 | 2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9350G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396708 | ||||||
chr20:44396910
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0003g0112 | 2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9148C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396910 | ||||||
chr20:44396933
|
A | C | 4 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-9125A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396933 | ||||||
chr20:44396955
|
T | C | 2 | a0001c0001t0001g0221a0001c0001t0003g0112 | 2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-9103T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396955 | ||||||
chr20:44396965
|
T | C | 24 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0003g0285others(21): Show | 24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.50-9093T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44396965 | ||||||
chr20:44397025
|
T | A | 1 | a0001c0001t0022g0088 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.50-9033T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397025 | ||||||
chr20:44397026
|
A | T | 1 | a0001c0001t0022g0088 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.50-9032A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397026 | ||||||
chr20:44397144
|
T | C | 134 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0121others(131): Show | 135 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.50-8914T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397144 | ||||||
chr20:44397272
|
C | T | 2 | a0001c0001t0001g0221a0001c0001t0003g0112 | 2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-8786C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397272 | ||||||
chr20:44397338
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0002g0031a0001c0001t0022g0060others(1): Show | 4 | HG02135.hp2 NA18612.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-8720G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397338 | ||||||
chr20:44397347
|
T | A | 2 | a0001c0001t0033g0277a0001c0001t0081g0305 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.50-8711T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397347 | ||||||
chr20:44397473
|
C | G | 1 | a0001c0001t0037g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.50-8585C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397473 | ||||||
chr20:44397973
|
T | A | 1 | a0001c0001t0017g0314 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.50-8085T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397973 | ||||||
chr20:44397976
|
T | C | 136 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0121others(133): Show | 137 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.50-8082T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397976 | ||||||
chr20:44397989
|
C | T | 271 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(268): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.50-8069C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44397989 | ||||||
chr20:44398035
|
C | T | 2 | a0001c0001t0030g0204a0001c0001t0030g0205 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.50-8023C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398035 | ||||||
chr20:44398148
|
G | A | 2 | a0001c0001t0001g0221a0001c0001t0003g0112 | 2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.50-7910G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398148 | ||||||
chr20:44398500
|
A | T | 1 | a0001c0001t0007g0029 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.50-7558A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398500 | ||||||
chr20:44398562
|
T | C | 2 | a0001c0001t0053g0004a0001c0001t0064g0180 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.50-7496T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398562 | ||||||
chr20:44398803
|
C | T | 1 | a0001c0001t0020g0159 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.50-7255C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398803 | ||||||
chr20:44398870
|
A | G | 116 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0053others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.50-7188A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44398870 | ||||||
chr20:44399114
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0006g0278a0001c0001t0013g0116others(2): Show | 5 | HG02602.hp1 HG02630.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-6944T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399114 | ||||||
chr20:44399210
|
CAT | C | 29 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0170others(26): Show | 29 | HG00741.hp2 HG01074.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.50-6846_50-6845del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44399210 | |||||
chr20:44399397
|
A | G | 226 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(223): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.50-6661A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399397 | ||||||
chr20:44399398
|
T | C | 34 | a0001c0001t0001g0103a0001c0001t0001g0121a0001c0001t0001g0170others(31): Show | 34 | HG00639.hp2 HG00741.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.50-6660T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399398 | ||||||
chr20:44399438
|
T | C | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.50-6620T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399438 | ||||||
chr20:44399531
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.50-6527A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399531 | ||||||
chr20:44399565
|
C | T | 1 | a0001c0001t0013g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.50-6493C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399565 | ||||||
chr20:44399603
|
G | A | 1 | a0001c0001t0056g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.50-6455G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399603 | ||||||
chr20:44399666
|
C | A | 47 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0001t0001g0182others(44): Show | 47 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.50-6392C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399666 | ||||||
chr20:44399701
|
C | G | 1 | a0001c0001t0003g0275 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.50-6357C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399701 | ||||||
chr20:44399718
|
C | T | 1 | a0001c0001t0020g0048 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.50-6340C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399718 | ||||||
chr20:44399750
|
A | G | 101 | a0001c0001t0001g0017a0001c0001t0001g0120a0001c0001t0001g0157others(98): Show | 102 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.50-6308A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399750 | ||||||
chr20:44399939
|
C | T | 6 | a0001c0001t0001g0255a0001c0001t0027g0010a0001c0001t0027g0011others(3): Show | 6 | HG00544.hp2 HG01891.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-6119C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44399939 | ||||||
chr20:44400231
|
G | A | 1 | a0001c0001t0011g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.50-5827G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400231 | ||||||
chr20:44400321
|
G | T | 1 | a0001c0003t0063g0081 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.50-5737G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400321 | ||||||
chr20:44400328
|
C | T | 4 | a0001c0001t0006g0057a0001c0001t0006g0073a0001c0001t0054g0066others(1): Show | 4 | HG01109.hp1 HG01169.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-5730C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400328 | ||||||
chr20:44400347
|
AGGG | A | 65 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0062others(62): Show | 65 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.50-5708_50-5706del others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44400347 | |||||
chr20:44400350
|
G | A | 1 | a0001c0001t0048g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.50-5708G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400350 | ||||||
chr20:44400364
|
C | T | 1 | a0001c0001t0003g0058 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.50-5694C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400364 | ||||||
chr20:44400468
|
C | T | 1 | a0002c0002t0001g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.50-5590C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400468 | ||||||
chr20:44400645
|
A | C | 175 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.50-5413A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400645 | ||||||
chr20:44400675
|
G | A | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-5383G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400675 | ||||||
chr20:44400741
|
G | A | 1 | a0001c0009t0082g0279 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.50-5317G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44400741 | ||||||
chr20:44401013
|
G | A | 1 | a0001c0001t0004g0167 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.50-5045G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401013 | ||||||
chr20:44401024
|
T | C | 13 | a0001c0001t0002g0022a0001c0001t0010g0014a0001c0001t0010g0015others(10): Show | 13 | HG02145.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.50-5034T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401024 | ||||||
chr20:44401353
|
G | A | 1 | a0001c0001t0004g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.50-4705G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401353 | ||||||
chr20:44401520
|
G | A | 1 | a0001c0014t0070g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.50-4538G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401520 | ||||||
chr20:44401671
|
A | C | 7 | a0001c0001t0002g0303a0001c0001t0017g0207a0001c0001t0017g0209others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.50-4387A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401671 | ||||||
chr20:44401718
|
G | A | 1 | a0001c0001t0025g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.50-4340G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401718 | ||||||
chr20:44401795
|
G | A | 63 | a0001c0001t0001g0062a0001c0001t0002g0039a0001c0001t0002g0043others(60): Show | 63 | HG00423.hp2 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.50-4263G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401795 | ||||||
chr20:44401831
|
G | A | 2 | a0001c0001t0037g0225a0001c0001t0100g0122 | 2 | HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.50-4227G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401831 | ||||||
chr20:44401844
|
A | T | 3 | a0001c0001t0028g0098a0001c0001t0050g0126a0001c0001t0064g0180 | 3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-4214A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44401844 | ||||||
chr20:44402073
|
T | C | 3 | a0001c0001t0028g0098a0001c0001t0050g0126a0001c0001t0064g0180 | 3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-3985T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402073 | ||||||
chr20:44402114
|
C | G | 3 | a0001c0001t0028g0098a0001c0001t0050g0126a0001c0001t0064g0180 | 3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-3944C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402114 | ||||||
chr20:44402114
|
C | T | 3 | a0001c0001t0003g0112a0001c0001t0003g0301a0005c0006t0023g0107 | 3 | HG00639.hp2 HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.50-3944C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402114 | ||||||
chr20:44402131
|
G | A | 2 | a0001c0001t0051g0030a0003c0004t0058g0082 | 2 | HG03942.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.50-3927G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402131 | ||||||
chr20:44402143
|
CTG | C | 8 | a0001c0001t0002g0303a0001c0001t0011g0257a0001c0001t0017g0207others(5): Show | 8 | HG01261.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.50-3908_50-3907del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44402143 | |||||
chr20:44402169
|
C | A | 41 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(38): Show | 41 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.50-3889C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402169 | ||||||
chr20:44402211
|
T | G | 3 | a0001c0001t0028g0098a0001c0001t0050g0126a0001c0001t0064g0180 | 3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-3847T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402211 | ||||||
chr20:44402226
|
T | C | 42 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(39): Show | 42 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.50-3832T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402226 | ||||||
chr20:44402271
|
G | A | 1 | a0001c0001t0004g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.50-3787G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402271 | ||||||
chr20:44402288
|
G | A | 1 | a0001c0001t0064g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.50-3770G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402288 | ||||||
chr20:44402316
|
C | T | 137 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(134): Show | 137 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.50-3742C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402316 | ||||||
chr20:44402453
|
C | T | 1 | a0001c0001t0016g0178 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.50-3605C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402453 | ||||||
chr20:44402652
|
A | G | 1 | a0001c0001t0025g0045 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.50-3406A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402652 | ||||||
chr20:44402897
|
C | T | 3 | a0001c0001t0028g0098a0001c0001t0050g0126a0001c0001t0064g0180 | 3 | HG00544.hp2 HG03579.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.50-3161C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44402897 | ||||||
chr20:44402917
|
A | AC | 4 | a0001c0001t0028g0098a0001c0001t0050g0126a0001c0001t0055g0254others(1): Show | 4 | HG00544.hp2 HG02723.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-3140dupC | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44402917 | |||||
chr20:44403004
|
G | A | 10 | a0001c0001t0001g0163a0001c0001t0001g0241a0001c0001t0001g0302others(7): Show | 10 | HG01069.hp1 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.50-3054G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403004 | ||||||
chr20:44403042
|
G | A | 1 | a0001c0001t0013g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.50-3016G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403042 | ||||||
chr20:44403113
|
G | A | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-2945G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403113 | ||||||
chr20:44403118
|
C | G | 1 | a0001c0001t0045g0012 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.50-2940C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403118 | ||||||
chr20:44403215
|
G | T | 30 | a0001c0001t0001g0127a0001c0001t0001g0157a0001c0001t0001g0164others(27): Show | 30 | HG01167.hp2 HG01358.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.50-2843G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403215 | ||||||
chr20:44403745
|
G | A | 1 | a0001c0001t0051g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.50-2313G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403745 | ||||||
chr20:44403745
|
G | C | 43 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(40): Show | 43 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.50-2313G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403745 | ||||||
chr20:44403806
|
T | A | 14 | a0001c0001t0001g0239a0001c0001t0002g0064a0001c0001t0003g0090others(11): Show | 14 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.50-2252T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403806 | ||||||
chr20:44403926
|
G | A | 1 | a0001c0001t0013g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.50-2132G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44403926 | ||||||
chr20:44404056
|
C | T | 2 | a0001c0001t0051g0030a0003c0004t0058g0082 | 2 | HG03942.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.50-2002C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404056 | ||||||
chr20:44404064
|
T | C | 1 | a0001c0001t0046g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-1994T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404064 | ||||||
chr20:44404227
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.50-1831G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404227 | ||||||
chr20:44404301
|
A | G | 2 | a0001c0001t0045g0012a0001c0001t0055g0254 | 2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.50-1757A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404301 | ||||||
chr20:44404365
|
A | G | 1 | a0001c0001t0052g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.50-1693A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404365 | ||||||
chr20:44404455
|
G | C | 112 | a0001c0001t0001g0062a0001c0001t0001g0121a0001c0001t0001g0170others(109): Show | 112 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.50-1603G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404455 | ||||||
chr20:44404518
|
G | A | 2 | a0001c0001t0011g0257a0001c0001t0056g0117 | 2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.50-1540G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404518 | ||||||
chr20:44404594
|
G | A | 55 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0110others(52): Show | 55 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.50-1464G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404594 | ||||||
chr20:44404613
|
T | G | 3 | a0001c0001t0019g0154a0001c0001t0019g0161a0001c0001t0019g0173 | 3 | HG02615.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.50-1445T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404613 | ||||||
chr20:44404672
|
G | T | 1 | a0001c0001t0035g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.50-1386G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404672 | ||||||
chr20:44404728
|
CTG | C | 43 | a0001c0001t0001g0127a0001c0001t0001g0157a0001c0001t0001g0163others(40): Show | 43 | HG01069.hp1 HG01167.hp2 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.50-1326_50-1325del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404728 | |||||
chr20:44404776
|
T | TGTGTTTG others(757): Show |
4 | a0001c0001t0001g0127a0001c0001t0001g0157a0001c0001t0001g0163others(1): Show | 4 | HG01358.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(764): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(771): Show |
1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(778): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(772): Show |
1 | a0001c0001t0035g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(779): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(769): Show |
1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(776): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(925): Show |
2 | a0001c0001t0045g0012a0001c0001t0055g0254 | 2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(932): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(769): Show |
3 | a0001c0001t0038g0318a0001c0001t0090g0106a0001c0003t0063g0081 | 3 | HG02055.hp2 HG02486.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(776): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(771): Show |
46 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0124others(43): Show | 46 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(43): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(778): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(773): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0120 | 2 | HG02135.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(780): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(739): Show |
2 | a0001c0001t0084g0099a0001c0001t0085g0183 | 2 | HG01256.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(746): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(755): Show |
50 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0071others(47): Show | 52 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(762): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(757): Show |
32 | a0001c0001t0001g0190a0001c0001t0002g0022a0001c0001t0004g0172others(29): Show | 32 | HG00544.hp2 HG01167.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(764): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(759): Show |
1 | a0001c0001t0051g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(766): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(732): Show |
4 | a0001c0001t0001g0241a0001c0001t0012g0228a0001c0001t0012g0240others(1): Show | 4 | HG01069.hp1 HG02647.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(739): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(722): Show |
5 | a0001c0001t0017g0207a0001c0001t0017g0209a0001c0001t0017g0314others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(729): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(720): Show |
1 | a0001c0001t0002g0303 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(727): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404776
|
T | TGTGTTTG others(734): Show |
2 | a0001c0001t0011g0257a0001c0001t0056g0117 | 2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(741): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404776 | |||||
chr20:44404777
|
G | GTGTTTGT others(765): Show |
1 | a0001c0001t0005g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(772): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404777 | |||||
chr20:44404778
|
T | TGTTTGTT others(765): Show |
1 | a0001c0001t0099g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(772): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404778
|
T | TGTTTGTT others(797): Show |
1 | a0001c0001t0069g0197 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(804): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404778
|
T | TGTTTGTT others(731): Show |
2 | a0001c0001t0003g0059a0001c0001t0042g0084 | 2 | NA18995.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(738): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404778
|
T | TGTTTGTT others(763): Show |
1 | a0001c0001t0002g0132 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(770): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404778
|
T | TGTTTGTT others(765): Show |
150 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(147): Show | 150 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.50-1278_50-1277ins others(772): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404778
|
T | TGTTTGTT others(753): Show |
1 | a0001c0001t0016g0178 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(760): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404778
|
T | TGTTTGTT others(767): Show |
1 | a0001c0001t0014g0119 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(774): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404778
|
T | TGTTTGTT others(763): Show |
1 | a0001c0001t0046g0021 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(770): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404778
|
T | TGTTTGTT others(769): Show |
1 | a0001c0001t0083g0166 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(776): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404778 | |||||
chr20:44404780
|
T | TTTGTTGA others(763): Show |
1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1278_50-1277ins others(770): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404780 | ||||||
chr20:44404781
|
G | T | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1277G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404781 | ||||||
chr20:44404786
|
C | T | 162 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(159): Show | 162 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.50-1272C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404786 | ||||||
chr20:44404788
|
T | C | 160 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(157): Show | 160 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.50-1270T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404788 | ||||||
chr20:44404790
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1268T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404790 | ||||||
chr20:44404793
|
C | A | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1265C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404793 | ||||||
chr20:44404793
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1265C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404793 | ||||||
chr20:44404797
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1261G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404797 | ||||||
chr20:44404806
|
G | GTGAATTG others(750): Show |
1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1252_50-1251ins others(757): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404806 | ||||||
chr20:44404808
|
A | T | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1250A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404808 | ||||||
chr20:44404825
|
A | G | 319 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.50-1233A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404825 | ||||||
chr20:44404854
|
G | GGT | 169 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(166): Show | 169 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.50-1196_50-1195dup others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404854 | |||||
chr20:44404864
|
C | T | 1 | a0005c0006t0023g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-1194C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404864 | ||||||
chr20:44404868
|
T | C | 1 | a0005c0006t0023g0107 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.50-1190T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404868 | ||||||
chr20:44404893
|
A | G | 319 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.50-1165A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404893 | ||||||
chr20:44404929
|
G | GGTGT | 158 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(155): Show | 158 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.50-1123_50-1120dup others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404929 | |||||
chr20:44404939
|
C | G | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1119C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404939 | ||||||
chr20:44404947
|
G | T | 319 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.50-1111G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404947 | ||||||
chr20:44404949
|
A | G | 319 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.50-1109A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404949 | ||||||
chr20:44404985
|
G | A | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1073G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404985 | ||||||
chr20:44404986
|
TGTGTGTG others(10): Show |
T | 1 | a0001c0001t0055g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.50-1063_50-1047del others(17): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44404986 | |||||
chr20:44404992
|
T | C | 4 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0013g0114others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-1066T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404992 | ||||||
chr20:44404998
|
T | A | 1 | a0001c0001t0099g0253 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.50-1060T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44404998 | ||||||
chr20:44405012
|
G | A | 55 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0110others(52): Show | 55 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.50-1046G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405012 | ||||||
chr20:44405012
|
G | T | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.50-1046G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405012 | ||||||
chr20:44405033
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.50-1025C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405033 | ||||||
chr20:44405044
|
T | TTGTGTGT others(15): Show |
153 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0062others(150): Show | 153 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.50-983_50-962dupGA others(20): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44405044 | |||||
chr20:44405083
|
GGTGCGTG others(22): Show |
G | 2 | a0001c0001t0045g0012a0001c0001t0055g0254 | 2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.50-961_50-933delCT others(27): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44405083 | |||||
chr20:44405170
|
T | C | 2 | a0001c0001t0001g0286a0001c0001t0071g0273 | 2 | HG01261.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.50-888T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405170 | ||||||
chr20:44405268
|
C | CAAATTTT others(2): Show |
53 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0110others(50): Show | 53 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.50-765_50-757dupTT others(7): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr20 | 44405268 | |||||
chr20:44405281
|
T | A | 1 | a0001c0001t0003g0027 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.50-777T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405281 | ||||||
chr20:44405290
|
T | G | 4 | a0001c0001t0045g0012a0001c0001t0051g0030a0001c0001t0055g0254others(1): Show | 4 | HG02723.hp1 HG02886.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-768T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405290 | ||||||
chr20:44405376
|
G | A | 103 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0053others(100): Show | 103 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.50-682G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405376 | ||||||
chr20:44405439
|
G | A | 42 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(39): Show | 42 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.50-619G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405439 | ||||||
chr20:44405476
|
C | A | 1 | a0001c0001t0061g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.50-582C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405476 | ||||||
chr20:44405484
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-574C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405484 | ||||||
chr20:44405531
|
A | T | 51 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0110others(48): Show | 51 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.50-527A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405531 | ||||||
chr20:44405700
|
A | G | 2 | a0001c0001t0051g0030a0003c0004t0058g0082 | 2 | HG03942.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.50-358A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405700 | ||||||
chr20:44405828
|
A | G | 268 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0053others(265): Show | 268 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(265): Show |
intron_variant | MODIFIER | c.50-230A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405828 | ||||||
chr20:44405832
|
C | T | 43 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(40): Show | 43 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.50-226C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405832 | ||||||
chr20:44405842
|
C | T | 2 | a0001c0001t0045g0012a0001c0001t0055g0254 | 2 | HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.50-216C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405842 | ||||||
chr20:44405873
|
C | G | 49 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(46): Show | 49 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.50-185C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44405873 | ||||||
chr20:44406020
|
T | C | 179 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0103others(176): Show | 179 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.50-38T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44406020 | ||||||
chr20:44406053
|
C | T | 55 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0110others(52): Show | 55 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(52): Show |
splice_region_variant&intron_variant | LOW | c.50-5C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 1/9 | chr20 | 44406053 | ||||||
chr20:44406440
|
C | T | 1 | a0001c0001t0052g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.224+208C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406440 | ||||||
chr20:44406498
|
C | T | 227 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0053others(224): Show | 227 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(224): Show |
intron_variant | MODIFIER | c.224+266C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406498 | ||||||
chr20:44406520
|
G | C | 270 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0053others(267): Show | 270 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(267): Show |
intron_variant | MODIFIER | c.224+288G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406520 | ||||||
chr20:44406650
|
C | T | 1 | a0001c0012t0008g0006 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.224+418C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406650 | ||||||
chr20:44406688
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.224+456G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44406688 | ||||||
chr20:44407103
|
A | G | 56 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0110others(53): Show | 56 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.225-278A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407103 | ||||||
chr20:44407140
|
C | T | 45 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0120others(42): Show | 45 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.225-241C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407140 | ||||||
chr20:44407154
|
A | C | 1 | a0001c0001t0051g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.225-227A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407154 | ||||||
chr20:44407182
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.225-199C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407182 | ||||||
chr20:44407200
|
A | T | 4 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0013g0114others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.225-181A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407200 | ||||||
chr20:44407298
|
C | T | 1 | a0001c0001t0004g0251 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.225-83C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 2/9 | chr20 | 44407298 | ||||||
chr20:44407494
|
C | T | 4 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0013g0114others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.319+19C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407494 | ||||||
chr20:44407711
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.319+236A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407711 | ||||||
chr20:44407757
|
T | TTG | 92 | a0001c0001t0001g0062a0001c0001t0001g0120a0001c0001t0001g0121others(89): Show | 92 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.319+316_319+317dup others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
T | TTGTG | 64 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0127others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.319+314_319+317dup others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
T | TTGTGTG | 18 | a0001c0001t0001g0212a0001c0001t0001g0241a0001c0001t0010g0208others(15): Show | 18 | HG00544.hp2 HG01261.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.319+312_319+317dup others(6): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
T | TTGTGTGT others(1): Show |
33 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(30): Show | 33 | HG00438.hp1 HG00621.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.319+310_319+317dup others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
T | TTGTGTGT others(3): Show |
14 | a0001c0001t0001g0141a0001c0001t0001g0302a0001c0001t0003g0058others(11): Show | 14 | HG00639.hp2 HG01255.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.319+308_319+317dup others(10): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
T | TTGTGTGT others(5): Show |
5 | a0001c0001t0001g0221a0001c0001t0003g0301a0001c0001t0004g0300others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.319+306_319+317dup others(12): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0087g0313 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.319+304_319+317dup others(14): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
TTG | T | 7 | a0001c0001t0001g0071a0001c0001t0001g0195a0001c0001t0004g0167others(4): Show | 7 | HG01081.hp2 HG01515.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+316_319+317del others(2): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
TTGTG | T | 7 | a0001c0001t0001g0170a0001c0001t0002g0252a0001c0001t0006g0057others(4): Show | 7 | HG01109.hp1 HG01169.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+314_319+317del others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407757
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.319+308_319+317del others(10): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44407757 | |||||
chr20:44407802
|
T | G | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.319+327T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407802 | ||||||
chr20:44407812
|
G | A | 165 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0053others(162): Show | 165 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.319+337G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407812 | ||||||
chr20:44407866
|
A | G | 1 | a0001c0001t0068g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.319+391A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44407866 | ||||||
chr20:44408009
|
A | G | 56 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0110others(53): Show | 56 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.319+534A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408009 | ||||||
chr20:44408037
|
A | C | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.319+562A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408037 | ||||||
chr20:44408051
|
T | G | 56 | a0001c0001t0001g0017a0001c0001t0001g0103a0001c0001t0001g0110others(53): Show | 56 | HG00099.hp1 HG00544.hp1 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.319+576T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408051 | ||||||
chr20:44408373
|
G | A | 56 | a0001c0001t0001g0121a0001c0001t0001g0170a0001c0001t0001g0182others(53): Show | 56 | HG00423.hp1 HG00597.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.319+898G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408373 | ||||||
chr20:44408512
|
G | T | 2 | a0001c0001t0033g0277a0001c0001t0081g0305 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.319+1037G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408512 | ||||||
chr20:44408720
|
C | G | 1 | a0001c0001t0003g0295 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.319+1245C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408720 | ||||||
chr20:44408725
|
A | T | 114 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0103others(111): Show | 114 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.319+1250A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408725 | ||||||
chr20:44408726
|
A | C | 114 | a0001c0001t0001g0017a0001c0001t0001g0053a0001c0001t0001g0103others(111): Show | 114 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.319+1251A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408726 | ||||||
chr20:44408739
|
A | T | 49 | a0001c0001t0001g0025a0001c0001t0001g0065a0001c0001t0001g0141others(46): Show | 49 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.319+1264A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408739 | ||||||
chr20:44408740
|
G | A | 57 | a0001c0001t0001g0121a0001c0001t0001g0182a0001c0001t0001g0190others(54): Show | 57 | HG00673.hp2 HG00741.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.319+1265G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408740 | ||||||
chr20:44408782
|
A | G | 51 | a0001c0001t0001g0025a0001c0001t0001g0065a0001c0001t0001g0141others(48): Show | 51 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.319+1307A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408782 | ||||||
chr20:44408786
|
T | G | 1 | a0001c0001t0004g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.319+1311T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408786 | ||||||
chr20:44408880
|
C | T | 1 | a0001c0001t0043g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+1405C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408880 | ||||||
chr20:44408932
|
C | T | 23 | a0001c0001t0001g0190a0001c0001t0001g0239a0001c0001t0002g0064others(20): Show | 23 | HG01433.hp1 HG01496.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.319+1457C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408932 | ||||||
chr20:44408953
|
G | C | 1 | a0001c0001t0006g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.319+1478G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44408953 | ||||||
chr20:44409000
|
C | G | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.319+1525C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409000 | ||||||
chr20:44409344
|
T | C | 8 | a0001c0001t0010g0208a0001c0001t0012g0187a0001c0001t0012g0188others(5): Show | 8 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.319+1869T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409344 | ||||||
chr20:44409351
|
T | C | 1 | a0001c0001t0068g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.319+1876T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409351 | ||||||
chr20:44409426
|
A | G | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.319+1951A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409426 | ||||||
chr20:44409446
|
T | C | 1 | a0001c0001t0085g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.319+1971T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409446 | ||||||
chr20:44409492
|
G | A | 1 | a0001c0001t0005g0199 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.319+2017G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409492 | ||||||
chr20:44409568
|
T | C | 211 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(208): Show | 212 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.319+2093T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409568 | ||||||
chr20:44409609
|
C | T | 73 | a0001c0001t0001g0221a0001c0001t0002g0024a0001c0001t0002g0039others(70): Show | 73 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.319+2134C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409609 | ||||||
chr20:44409832
|
G | A | 1 | a0001c0001t0043g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.319+2357G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409832 | ||||||
chr20:44409839
|
CT | C | 130 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0036others(127): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.319+2380delT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44409839 | |||||
chr20:44409839
|
CTT | C | 173 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(170): Show | 173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.319+2379_319+2380d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44409839 | |||||
chr20:44409907
|
G | A | 1 | a0001c0001t0003g0223 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.319+2432G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409907 | ||||||
chr20:44409919
|
C | A | 174 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(171): Show | 174 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.319+2444C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409919 | ||||||
chr20:44409988
|
C | T | 71 | a0001c0001t0001g0221a0001c0001t0002g0024a0001c0001t0002g0039others(68): Show | 71 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.319+2513C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44409988 | ||||||
chr20:44410028
|
G | T | 1 | a0001c0001t0056g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.319+2553G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410028 | ||||||
chr20:44410051
|
G | T | 11 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0013g0114others(8): Show | 11 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.319+2576G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410051 | ||||||
chr20:44410064
|
T | C | 191 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(188): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.319+2589T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410064 | ||||||
chr20:44410079
|
C | T | 71 | a0001c0001t0001g0221a0001c0001t0002g0024a0001c0001t0002g0039others(68): Show | 71 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.319+2604C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410079 | ||||||
chr20:44410080
|
G | A | 47 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(44): Show | 47 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.319+2605G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410080 | ||||||
chr20:44410128
|
C | T | 96 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(93): Show | 96 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.319+2653C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410128 | ||||||
chr20:44410142
|
T | C | 101 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.319+2667T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410142 | ||||||
chr20:44410304
|
C | A | 71 | a0001c0001t0001g0221a0001c0001t0002g0024a0001c0001t0002g0039others(68): Show | 71 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.319+2829C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410304 | ||||||
chr20:44410400
|
G | A | 15 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(12): Show | 16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.319+2925G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410400 | ||||||
chr20:44410605
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0083g0166 | 2 | HG01074.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.320-3089A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410605 | ||||||
chr20:44410623
|
C | T | 15 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(12): Show | 16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-3071C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410623 | ||||||
chr20:44410720
|
C | A | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.320-2974C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410720 | ||||||
chr20:44410735
|
G | A | 26 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(23): Show | 27 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-2959G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410735 | ||||||
chr20:44410797
|
C | G | 1 | a0001c0001t0043g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.320-2897C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410797 | ||||||
chr20:44410842
|
C | T | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.320-2852C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410842 | ||||||
chr20:44410897
|
G | C | 49 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(46): Show | 49 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.320-2797G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44410897 | ||||||
chr20:44411083
|
G | T | 4 | a0001c0001t0023g0003a0001c0001t0044g0115a0001c0001t0046g0021others(1): Show | 4 | HG01069.hp1 HG02809.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-2611G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411083 | ||||||
chr20:44411146
|
C | T | 11 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0013g0114others(8): Show | 11 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.320-2548C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411146 | ||||||
chr20:44411211
|
C | T | 26 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(23): Show | 27 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-2483C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411211 | ||||||
chr20:44411387
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.320-2307G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411387 | ||||||
chr20:44411497
|
C | T | 25 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(22): Show | 26 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.320-2197C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411497 | ||||||
chr20:44411540
|
G | T | 10 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0013g0114others(7): Show | 10 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.320-2154G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411540 | ||||||
chr20:44411553
|
C | A | 26 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(23): Show | 27 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-2141C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411553 | ||||||
chr20:44411566
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.320-2128C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411566 | ||||||
chr20:44411585
|
G | A | 11 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0013g0114others(8): Show | 11 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.320-2109G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411585 | ||||||
chr20:44411639
|
A | G | 1 | a0001c0001t0055g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.320-2055A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411639 | ||||||
chr20:44411648
|
C | T | 98 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(95): Show | 98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.320-2046C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411648 | ||||||
chr20:44411791
|
T | C | 2 | a0001c0001t0002g0229a0001c0001t0020g0244 | 2 | NA18951.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.320-1903T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411791 | ||||||
chr20:44411796
|
C | T | 15 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(12): Show | 16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-1898C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411796 | ||||||
chr20:44411853
|
C | T | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.320-1841C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411853 | ||||||
chr20:44411891
|
C | CA | 14 | a0001c0001t0001g0302a0001c0001t0002g0303a0001c0001t0004g0300others(11): Show | 14 | HG01074.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.320-1788dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44411891 | |||||
chr20:44411907
|
T | A | 19 | a0001c0001t0001g0170a0001c0001t0006g0278a0001c0001t0009g0125others(16): Show | 19 | HG00280.hp1 HG00741.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.320-1787T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411907 | ||||||
chr20:44411908
|
T | G | 1 | a0001c0001t0055g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.320-1786T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411908 | ||||||
chr20:44411929
|
C | T | 130 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.320-1765C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411929 | ||||||
chr20:44411965
|
G | C | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.320-1729G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44411965 | ||||||
chr20:44412057
|
G | GA | 17 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0005g0072others(14): Show | 17 | HG01516.hp1 HG01517.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.320-1626dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44412057 | |||||
chr20:44412057
|
G | GAA | 15 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(12): Show | 16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-1627_320-1626d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44412057 | |||||
chr20:44412087
|
G | T | 1 | a0001c0001t0013g0184 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.320-1607G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412087 | ||||||
chr20:44412092
|
T | C | 30 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(27): Show | 31 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.320-1602T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412092 | ||||||
chr20:44412153
|
C | T | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.320-1541C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412153 | ||||||
chr20:44412275
|
A | C | 102 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(99): Show | 102 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.320-1419A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412275 | ||||||
chr20:44412359
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.320-1335A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412359 | ||||||
chr20:44412362
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0002g0303 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.320-1332G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412362 | ||||||
chr20:44412455
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.320-1239G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412455 | ||||||
chr20:44412480
|
C | T | 1 | a0001c0001t0014g0087 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.320-1214C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412480 | ||||||
chr20:44412491
|
G | A | 179 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0065others(176): Show | 179 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.320-1203G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412491 | ||||||
chr20:44412491
|
G | T | 15 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(12): Show | 16 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.320-1203G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412491 | ||||||
chr20:44412498
|
G | C | 5 | a0001c0001t0004g0104a0001c0001t0004g0172a0001c0001t0008g0134others(2): Show | 5 | HG01361.hp1 HG01884.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-1196G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412498 | ||||||
chr20:44412552
|
G | A | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-1142G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412552 | ||||||
chr20:44412594
|
C | G | 30 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(27): Show | 31 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.320-1100C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412594 | ||||||
chr20:44412700
|
G | A | 26 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(23): Show | 27 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.320-994G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412700 | ||||||
chr20:44412747
|
G | A | 1 | a0001c0001t0039g0118 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.320-947G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412747 | ||||||
chr20:44412755
|
T | C | 4 | a0001c0001t0043g0307a0001c0003t0063g0081a0001c0003t0066g0315others(1): Show | 4 | HG02486.hp2 HG02630.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.320-939T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412755 | ||||||
chr20:44412801
|
T | C | 15 | a0001c0001t0001g0302a0001c0001t0004g0300a0001c0001t0013g0114others(12): Show | 15 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.320-893T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412801 | ||||||
chr20:44412811
|
G | A | 1 | a0001c0001t0052g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.320-883G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412811 | ||||||
chr20:44412846
|
G | A | 1 | a0001c0001t0043g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.320-848G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412846 | ||||||
chr20:44412906
|
T | C | 3 | a0001c0001t0003g0028a0001c0001t0028g0098a0001c0001t0028g0233 | 3 | HG02015.hp1 NA18952.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.320-788T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412906 | ||||||
chr20:44412951
|
C | T | 108 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(105): Show | 108 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.320-743C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412951 | ||||||
chr20:44412961
|
T | C | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-733T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412961 | ||||||
chr20:44412977
|
C | T | 1 | a0001c0001t0003g0100 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.320-717C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44412977 | ||||||
chr20:44413018
|
T | TC | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-674dupC | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr20 | 44413018 | |||||
chr20:44413092
|
G | A | 100 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0071others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.320-602G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413092 | ||||||
chr20:44413103
|
C | T | 5 | a0001c0001t0002g0043a0001c0001t0002g0076a0001c0001t0002g0101others(2): Show | 5 | HG02027.hp2 HG02056.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-591C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413103 | ||||||
chr20:44413170
|
G | A | 5 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0003t0063g0081others(2): Show | 5 | HG02486.hp2 HG02630.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.320-524G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413170 | ||||||
chr20:44413261
|
T | C | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-433T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413261 | ||||||
chr20:44413328
|
C | T | 1 | a0001c0001t0035g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.320-366C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413328 | ||||||
chr20:44413333
|
A | G | 1 | a0001c0001t0002g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.320-361A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413333 | ||||||
chr20:44413383
|
G | T | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-311G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413383 | ||||||
chr20:44413424
|
A | G | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-270A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413424 | ||||||
chr20:44413451
|
C | T | 6 | a0001c0001t0023g0003a0001c0001t0044g0115a0001c0001t0046g0021others(3): Show | 6 | HG02486.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.320-243C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413451 | ||||||
chr20:44413490
|
C | G | 27 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(24): Show | 28 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.320-204C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413490 | ||||||
chr20:44413594
|
C | T | 4 | a0001c0001t0023g0003a0001c0001t0044g0115a0001c0001t0046g0021others(1): Show | 4 | HG02809.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-100C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413594 | ||||||
chr20:44413647
|
T | C | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-47T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413647 | ||||||
chr20:44413660
|
T | C | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.320-34T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 3/9 | chr20 | 44413660 | ||||||
chr20:44413905
|
G | C | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.426+105G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44413905 | ||||||
chr20:44413940
|
C | G | 27 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(24): Show | 28 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.426+140C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44413940 | ||||||
chr20:44413966
|
C | A | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.426+166C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44413966 | ||||||
chr20:44413975
|
G | A | 3 | a0001c0003t0063g0081a0001c0003t0066g0315a0003c0004t0058g0082 | 3 | HG02486.hp2 HG02630.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.426+175G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44413975 | ||||||
chr20:44414221
|
T | C | 1 | a0001c0001t0031g0155 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.427-286T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414221 | ||||||
chr20:44414284
|
G | A | 1 | a0001c0001t0003g0265 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.427-223G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414284 | ||||||
chr20:44414310
|
A | C | 31 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.427-197A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414310 | ||||||
chr20:44414411
|
C | G | 18 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(15): Show | 19 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.427-96C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414411 | ||||||
chr20:44414455
|
G | A | 29 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0174others(26): Show | 30 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.427-52G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414455 | ||||||
chr20:44414459
|
G | A | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.427-48G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414459 | ||||||
chr20:44414478
|
C | T | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.427-29C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414478 | ||||||
chr20:44414487
|
C | T | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.427-20C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414487 | ||||||
chr20:44414503
|
G | A | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | splice_region_variant&intron_variant | LOW | c.427-4G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 4/9 | chr20 | 44414503 | ||||||
chr20:44414666
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG03654.hp1 | splice_region_variant&intron_variant | LOW | c.582+4A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44414666 | ||||||
chr20:44415037
|
G | T | 6 | a0001c0001t0023g0003a0001c0001t0044g0115a0001c0001t0046g0021others(3): Show | 6 | HG01069.hp1 HG02723.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.582+375G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415037 | ||||||
chr20:44415088
|
A | G | 1 | a0001c0001t0084g0099 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.582+426A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415088 | ||||||
chr20:44415208
|
G | A | 2 | a0001c0001t0002g0070a0001c0001t0002g0113 | 2 | HG03017.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.582+546G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415208 | ||||||
chr20:44415421
|
G | A | 1 | a0001c0001t0043g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.582+759G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415421 | ||||||
chr20:44415567
|
T | C | 311 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.582+905T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415567 | ||||||
chr20:44415722
|
C | T | 117 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(114): Show | 118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.582+1060C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44415722 | ||||||
chr20:44416058
|
G | A | 2 | a0001c0001t0002g0022a0001c0001t0034g0308 | 2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.582+1396G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416058 | ||||||
chr20:44416119
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.582+1457C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416119 | ||||||
chr20:44416153
|
A | G | 1 | a0001c0001t0038g0318 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.582+1491A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416153 | ||||||
chr20:44416180
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.582+1518G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416180 | ||||||
chr20:44416290
|
C | T | 2 | a0001c0001t0038g0318a0003c0004t0058g0082 | 2 | HG03225.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.582+1628C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416290 | ||||||
chr20:44416423
|
G | A | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.582+1761G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416423 | ||||||
chr20:44416443
|
C | G | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.582+1781C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416443 | ||||||
chr20:44416763
|
T | C | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.583-1662T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416763 | ||||||
chr20:44416767
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.583-1658G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416767 | ||||||
chr20:44416810
|
T | C | 14 | a0001c0001t0006g0001a0001c0001t0006g0057a0001c0001t0006g0073others(11): Show | 15 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.583-1615T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416810 | ||||||
chr20:44416856
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA18966.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.583-1569C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44416856 | ||||||
chr20:44417093
|
A | G | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.583-1332A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417093 | ||||||
chr20:44417158
|
G | GC | 132 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.583-1267_583-1266i others(3): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417158 | ||||||
chr20:44417389
|
T | C | 13 | a0001c0001t0017g0207a0001c0001t0017g0209a0001c0001t0017g0314others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.583-1036T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417389 | ||||||
chr20:44417405
|
T | G | 133 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(130): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.583-1020T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417405 | ||||||
chr20:44417424
|
C | T | 1 | a0001c0001t0097g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.583-1001C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417424 | ||||||
chr20:44417448
|
C | G | 1 | a0001c0001t0004g0298 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.583-977C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417448 | ||||||
chr20:44417538
|
C | T | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-887C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417538 | ||||||
chr20:44417801
|
G | A | 11 | a0001c0001t0017g0207a0001c0001t0017g0209a0001c0001t0017g0314others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.583-624G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417801 | ||||||
chr20:44417838
|
G | A | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-587G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417838 | ||||||
chr20:44417841
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0036 | 2 | HG00140.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.583-584C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417841 | ||||||
chr20:44417968
|
C | CA | 9 | a0001c0001t0003g0259a0001c0001t0004g0046a0001c0001t0004g0085others(6): Show | 9 | HG00544.hp2 HG02055.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.583-440dupA | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr20 | 44417968 | |||||
chr20:44417992
|
C | G | 2 | a0001c0001t0008g0007a0001c0001t0008g0067 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.583-433C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417992 | ||||||
chr20:44417994
|
G | T | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.583-431G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44417994 | ||||||
chr20:44418033
|
G | T | 1 | a0001c0001t0006g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.583-392G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44418033 | ||||||
chr20:44418044
|
G | A | 1 | a0001c0001t0026g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.583-381G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44418044 | ||||||
chr20:44418220
|
G | A | 1 | a0001c0001t0060g0096 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.583-205G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44418220 | ||||||
chr20:44418289
|
T | C | 36 | a0001c0001t0001g0062a0001c0001t0001g0120a0001c0001t0001g0201others(33): Show | 36 | HG00544.hp1 HG02027.hp1 HG02074.hp1 others(33): Show |
intron_variant | MODIFIER | c.583-136T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 5/9 | chr20 | 44418289 | ||||||
chr20:44418653
|
A | G | 131 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.670+141A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418653 | ||||||
chr20:44418708
|
G | A | 14 | a0001c0001t0006g0001a0001c0001t0006g0057a0001c0001t0006g0073others(11): Show | 15 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+196G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418708 | ||||||
chr20:44418871
|
G | A | 13 | a0001c0001t0006g0001a0001c0001t0006g0057a0001c0001t0006g0073others(10): Show | 14 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.670+359G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418871 | ||||||
chr20:44418895
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.670+383C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418895 | ||||||
chr20:44418903
|
G | C | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+391G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44418903 | ||||||
chr20:44419149
|
C | T | 2 | a0001c0001t0002g0229a0001c0001t0020g0244 | 2 | NA18951.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.671-572C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419149 | ||||||
chr20:44419194
|
A | G | 1 | a0001c0001t0043g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.671-527A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419194 | ||||||
chr20:44419495
|
T | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG01167.hp1 HG01169.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.671-226T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419495 | ||||||
chr20:44419506
|
C | G | 1 | a0001c0011t0080g0227 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.671-215C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419506 | ||||||
chr20:44419633
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.671-88G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 6/9 | chr20 | 44419633 | ||||||
chr20:44420003
|
G | A | 1 | a0001c0001t0064g0180 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.826+127G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420003 | ||||||
chr20:44420045
|
A | C | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.826+169A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420045 | ||||||
chr20:44420045
|
A | G | 131 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.826+169A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420045 | ||||||
chr20:44420106
|
C | A | 1 | a0001c0001t0002g0055 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.826+230C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420106 | ||||||
chr20:44420204
|
C | T | 1 | a0001c0001t0051g0030 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.826+328C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420204 | ||||||
chr20:44420205
|
G | A | 11 | a0001c0001t0017g0207a0001c0001t0017g0209a0001c0001t0017g0314others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+329G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420205 | ||||||
chr20:44420227
|
G | A | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+351G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420227 | ||||||
chr20:44420352
|
T | C | 1 | a0001c0001t0013g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.826+476T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420352 | ||||||
chr20:44420480
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.826+604T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420480 | ||||||
chr20:44420518
|
A | G | 1 | a0001c0001t0028g0098 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.826+642A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420518 | ||||||
chr20:44420536
|
T | A | 95 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.826+660T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420536 | ||||||
chr20:44420608
|
C | T | 2 | a0001c0001t0012g0228a0001c0001t0012g0240 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.826+732C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420608 | ||||||
chr20:44420678
|
A | G | 179 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.826+802A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420678 | ||||||
chr20:44420771
|
T | C | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.826+895T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420771 | ||||||
chr20:44420873
|
C | T | 1 | a0001c0001t0086g0026 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.826+997C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420873 | ||||||
chr20:44420936
|
A | G | 2 | a0001c0001t0003g0094a0001c0001t0003g0095 | 2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.826+1060A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44420936 | ||||||
chr20:44421132
|
TTA | T | 11 | a0001c0001t0017g0207a0001c0001t0017g0209a0001c0001t0017g0314others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+1258_826+1259d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44421132 | |||||
chr20:44421147
|
T | C | 1 | a0001c0001t0048g0299 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.826+1271T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421147 | ||||||
chr20:44421489
|
C | G | 1 | a0001c0001t0008g0067 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.826+1613C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421489 | ||||||
chr20:44421728
|
T | G | 132 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.826+1852T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421728 | ||||||
chr20:44421767
|
A | G | 3 | a0001c0001t0003g0112a0001c0001t0003g0301a0005c0006t0023g0107 | 3 | HG00639.hp2 HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.826+1891A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421767 | ||||||
chr20:44421773
|
G | GTA | 6 | a0001c0001t0004g0300a0001c0001t0028g0098a0001c0001t0028g0233others(3): Show | 6 | HG01515.hp1 HG01517.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.826+1908_826+1909d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44421773 | |||||
chr20:44421773
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0163 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.826+1917_826+1936d others(22): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44421773 | |||||
chr20:44421773
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0052g0158 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.826+1909_826+1910i others(24): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44421773 | |||||
chr20:44421785
|
A | T | 1 | a0001c0001t0043g0307 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.826+1909A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421785 | ||||||
chr20:44421843
|
C | T | 3 | a0001c0001t0019g0154a0001c0001t0019g0161a0001c0001t0019g0173 | 3 | HG02615.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.826+1967C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421843 | ||||||
chr20:44421940
|
T | A | 1 | a0001c0001t0096g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.826+2064T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44421940 | ||||||
chr20:44422036
|
T | A | 1 | a0001c0001t0001g0267 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.827-1982T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422036 | ||||||
chr20:44422092
|
C | T | 8 | a0001c0001t0017g0207a0001c0001t0017g0209a0001c0001t0017g0314others(5): Show | 8 | HG01891.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.827-1926C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422092 | ||||||
chr20:44422121
|
T | G | 131 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.827-1897T>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422121 | ||||||
chr20:44422130
|
C | T | 2 | a0001c0001t0005g0050a0007c0008t0005g0262 | 2 | HG02155.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.827-1888C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422130 | ||||||
chr20:44422142
|
A | G | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1876A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422142 | ||||||
chr20:44422202
|
G | T | 1 | a0001c0001t0085g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.827-1816G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422202 | ||||||
chr20:44422214
|
G | A | 1 | a0001c0001t0006g0249 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.827-1804G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422214 | ||||||
chr20:44422341
|
A | C | 135 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.827-1677A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422341 | ||||||
chr20:44422343
|
C | G | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.827-1675C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422343 | ||||||
chr20:44422557
|
C | T | 14 | a0001c0001t0006g0001a0001c0001t0006g0057a0001c0001t0006g0073others(11): Show | 15 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.827-1461C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422557 | ||||||
chr20:44422573
|
T | C | 135 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.827-1445T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422573 | ||||||
chr20:44422696
|
A | AAT | 14 | a0001c0001t0001g0127a0001c0001t0001g0157a0001c0001t0001g0163others(11): Show | 14 | HG01261.hp1 HG01358.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.827-1308_827-1307d others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr20 | 44422696 | |||||
chr20:44422714
|
C | A | 1 | a0001c0001t0002g0252 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.827-1304C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422714 | ||||||
chr20:44422728
|
G | A | 2 | a0001c0001t0001g0302a0001c0001t0013g0114 | 2 | HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.827-1290G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422728 | ||||||
chr20:44422758
|
C | T | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.827-1260C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422758 | ||||||
chr20:44422767
|
C | T | 1 | a0002c0002t0002g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.827-1251C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422767 | ||||||
chr20:44422931
|
G | A | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1087G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44422931 | ||||||
chr20:44423057
|
C | A | 1 | a0001c0001t0050g0126 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.827-961C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423057 | ||||||
chr20:44423146
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.827-872G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423146 | ||||||
chr20:44423230
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA18966.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.827-788C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423230 | ||||||
chr20:44423316
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.827-702A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423316 | ||||||
chr20:44423472
|
A | G | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.827-546A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423472 | ||||||
chr20:44423508
|
A | C | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.827-510A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423508 | ||||||
chr20:44423930
|
T | C | 148 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.827-88T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423930 | ||||||
chr20:44423974
|
G | C | 1 | a0001c0001t0087g0313 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.827-44G>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 7/9 | chr20 | 44423974 | ||||||
chr20:44424460
|
C | T | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1063+206C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424460 | ||||||
chr20:44424500
|
A | C | 3 | a0001c0001t0019g0154a0001c0001t0019g0161a0001c0001t0019g0173 | 3 | HG02615.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1063+246A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424500 | ||||||
chr20:44424671
|
A | G | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+417A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424671 | ||||||
chr20:44424691
|
C | T | 1 | a0001c0001t0004g0165 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1063+437C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424691 | ||||||
chr20:44424948
|
A | T | 129 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1063+694A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44424948 | ||||||
chr20:44425020
|
C | A | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1063+766C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425020 | ||||||
chr20:44425023
|
C | G | 1 | a0001c0001t0004g0224 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1063+769C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425023 | ||||||
chr20:44425151
|
T | C | 1 | a0001c0001t0020g0048 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1063+897T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425151 | ||||||
chr20:44425598
|
G | T | 1 | a0001c0001t0002g0203 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1063+1344G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425598 | ||||||
chr20:44425633
|
T | C | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063+1379T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425633 | ||||||
chr20:44425656
|
C | CT | 46 | a0001c0001t0001g0025a0001c0001t0002g0133a0001c0001t0003g0028others(43): Show | 46 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1063+1418dupT | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr20 | 44425656 | |||||
chr20:44425656
|
C | CTTT | 7 | a0001c0001t0001g0062a0001c0001t0001g0071a0001c0001t0001g0215others(4): Show | 7 | HG00323.hp1 HG01081.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063+1416_1063+141 others(7): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr20 | 44425656 | |||||
chr20:44425656
|
C | CTTTT | 90 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1063+1415_1063+141 others(8): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr20 | 44425656 | |||||
chr20:44425656
|
C | CTTTTT | 6 | a0001c0001t0001g0272a0001c0001t0004g0046a0001c0001t0055g0254others(3): Show | 6 | HG00735.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1063+1414_1063+141 others(9): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr20 | 44425656 | |||||
chr20:44425801
|
C | T | 73 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(70): Show | 73 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1063+1547C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425801 | ||||||
chr20:44425841
|
A | G | 103 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.1063+1587A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425841 | ||||||
chr20:44425843
|
A | G | 86 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.1063+1589A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44425843 | ||||||
chr20:44426018
|
GCTGTTGA others(155): Show |
G | 1 | a0001c0001t0097g0310 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1063+1765_1063+192 others(4): Show |
HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426018 | ||||||
chr20:44426020
|
T | A | 96 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1063+1766T>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426020 | ||||||
chr20:44426190
|
A | G | 1 | a0001c0001t0003g0296 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1063+1936A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426190 | ||||||
chr20:44426231
|
A | G | 96 | a0001c0001t0001g0017a0001c0001t0001g0032a0001c0001t0001g0036others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.1063+1977A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426231 | ||||||
chr20:44426239
|
G | T | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1063+1985G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426239 | ||||||
chr20:44426526
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1064-1809G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426526 | ||||||
chr20:44426785
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1064-1550C>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44426785 | ||||||
chr20:44427064
|
G | A | 1 | a0001c0001t0004g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1064-1271G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427064 | ||||||
chr20:44427177
|
A | T | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1064-1158A>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427177 | ||||||
chr20:44427204
|
A | G | 1 | a0008c0005t0025g0037 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1064-1131A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427204 | ||||||
chr20:44427457
|
T | C | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-878T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427457 | ||||||
chr20:44427509
|
G | T | 132 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1064-826G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427509 | ||||||
chr20:44427767
|
G | A | 1 | a0001c0011t0080g0227 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1064-568G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427767 | ||||||
chr20:44427845
|
T | C | 2 | a0001c0003t0063g0081a0001c0003t0066g0315 | 2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1064-490T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427845 | ||||||
chr20:44427922
|
T | C | 47 | a0001c0001t0001g0170a0001c0001t0006g0001a0001c0001t0006g0057others(44): Show | 48 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1064-413T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427922 | ||||||
chr20:44427925
|
G | A | 1 | a0001c0001t0053g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1064-410G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44427925 | ||||||
chr20:44428092
|
A | G | 4 | a0001c0001t0028g0098a0001c0001t0028g0233a0001c0001t0052g0158others(1): Show | 4 | HG03453.hp2 HG03942.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1064-243A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 8/9 | chr20 | 44428092 | ||||||
chr20:44428840
|
G | T | 160 | a0001c0001t0001g0103a0001c0001t0001g0190a0001c0001t0001g0272others(157): Show | 161 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1216+353G>T | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44428840 | ||||||
chr20:44429074
|
G | A | 1 | a0001c0001t0008g0002 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1217-449G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429074 | ||||||
chr20:44429154
|
A | G | 1 | a0001c0001t0022g0060 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1217-369A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429154 | ||||||
chr20:44429180
|
C | A | 150 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(147): Show | 151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1217-343C>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429180 | ||||||
chr20:44429191
|
A | G | 1 | a0001c0001t0056g0117 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1217-332A>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429191 | ||||||
chr20:44429206
|
G | A | 3 | a0001c0001t0027g0010a0001c0001t0027g0011a0001c0001t0049g0009 | 3 | HG01891.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1217-317G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429206 | ||||||
chr20:44429226
|
G | A | 1 | a0001c0001t0023g0003 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1217-297G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429226 | ||||||
chr20:44429344
|
G | A | 1 | a0003c0004t0058g0082 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1217-179G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429344 | ||||||
chr20:44429372
|
A | C | 16 | a0001c0001t0006g0001a0001c0001t0006g0057a0001c0001t0006g0073others(13): Show | 17 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1217-151A>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429372 | ||||||
chr20:44429378
|
T | C | 119 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(116): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1217-145T>C | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429378 | ||||||
chr20:44429440
|
G | A | 6 | a0001c0001t0017g0207a0001c0001t0017g0209a0001c0001t0017g0314others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1217-83G>A | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429440 | ||||||
chr20:44429456
|
C | G | 150 | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0032others(147): Show | 151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1217-67C>G | HNF4A | ENSG00000101076.20 | transcript | ENST00000316673.9 | protein_coding | 9/9 | chr20 | 44429456 |