geneid | 4800 |
---|---|
ensemblid | ENSG00000001167.15 |
hgncid | 7804 |
symbol | NFYA |
name | nuclear transcription factor Y subunit alpha |
refseq_nuc | NM_002505.5 |
refseq_prot | NP_002496.1 |
ensembl_nuc | ENST00000341376.11 |
ensembl_prot | ENSP00000345702.6 |
mane_status | MANE Select |
chr | chr6 |
start | 41072974 |
end | 41102403 |
strand | + |
ver | v1.2 |
region | chr6:41072974-41102403 |
region5000 | chr6:41067974-41107403 |
regionname0 | NFYA_chr6_41072974_41102403 |
regionname5000 | NFYA_chr6_41067974_41107403 |
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 | 347 | 321 | 90 | 52 | 125 | 12 | 40 | 105 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0002 | 0/0 | 347 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0003 | 0/0 | 347 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0004 | 0/0 | 347 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
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 | 1044 | 312 | 87 | 52 | 120 | 12 | 39 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
c0002 | 0/0 | 1044 | 5 | 0 | 0 | 5 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
c0003 | 0/0 | 1044 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
c0004 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
c0005 | 0/0 | 1044 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
c0006 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
c0007 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
c0008 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 5166 | 205 | 31 | 44 | 86 | 10 | 32 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0002 | 0/0 | 5166 | 25 | 0 | 0 | 25 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0003 | 0/0 | 5166 | 18 | 14 | 2 | 0 | 0 | 2 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0004 | 0/0 | 5166 | 16 | 16 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0005 | 0/0 | 5165 | 6 | 0 | 0 | 6 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0006 | 0/0 | 5166 | 6 | 6 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0007 | 0/0 | 5165 | 5 | 5 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0008 | 0/0 | 5164 | 5 | 0 | 5 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0009 | 0/0 | 5166 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0010 | 0/0 | 5166 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0011 | 0/0 | 5166 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0012 | 0/0 | 5166 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0013 | 0/0 | 5166 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0014 | 0/0 | 5166 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0015 | 0/0 | 5149 | 2 | 0 | 0 | 1 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0016 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0017 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0018 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0019 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0020 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0021 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0022 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0023 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0024 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0025 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0026 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0027 | 0/0 | 5165 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0028 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0029 | 0/0 | 5165 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0030 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0031 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0032 | 0/0 | 5164 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0033 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0034 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0035 | 0/0 | 5166 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0036 | 0/0 | 5166 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0037 | 0/0 | 5149 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
t0038 | 0/0 | 5166 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
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 | 36 | 3 | 12 | 9 | 5 | 7 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0002 | 0/0 | 34 | 1 | 9 | 13 | 3 | 8 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0003 | 0/0 | 32 | 0 | 2 | 26 | 0 | 4 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0004 | 0/0 | 24 | 0 | 0 | 24 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0005 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0006 | 0/0 | 9 | 1 | 1 | 6 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0008 | 0/0 | 6 | 1 | 1 | 3 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0009 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0023 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
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 | 1044 | 312 | 87 | 52 | 120 | 12 | 39 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0002 | 0/0 | 1044 | 5 | 0 | 0 | 5 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0003 | 0/0 | 1044 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0005 | 0/0 | 1044 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0008 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0002c0007 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0003c0006 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0004c0004 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 6209 | 196 | 29 | 44 | 80 | 10 | 31 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0002 | 0/0 | 6209 | 25 | 0 | 0 | 25 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0003 | 0/0 | 6209 | 18 | 14 | 2 | 0 | 0 | 2 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0004 | 0/0 | 6209 | 16 | 16 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0005 | 0/0 | 6208 | 6 | 0 | 0 | 6 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0006 | 0/0 | 6209 | 5 | 5 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0007 | 0/0 | 6208 | 4 | 4 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0008 | 0/0 | 6207 | 5 | 0 | 5 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0009 | 0/0 | 6209 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0010 | 0/0 | 6209 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0011 | 0/0 | 6209 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0012 | 0/0 | 6209 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0013 | 0/0 | 6209 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0014 | 0/0 | 6209 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0015 | 0/0 | 6192 | 2 | 0 | 0 | 1 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0016 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0017 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0019 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0020 | 0/0 | 6208 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0021 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0022 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0023 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0024 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0025 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0026 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0027 | 0/0 | 6208 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0028 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0029 | 0/0 | 6208 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0030 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0031 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0032 | 0/0 | 6207 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0033 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0034 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0035 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0036 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0037 | 0/0 | 6192 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0001t0038 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0002t0001 | 0/0 | 6209 | 5 | 0 | 0 | 5 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0003t0001 | 0/0 | 6209 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0005t0001 | 0/0 | 6209 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0001c0008t0018 | 0/0 | 6208 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0002c0007t0007 | 0/0 | 6208 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0003c0006t0006 | 0/0 | 6209 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
a0004c0004t0001 | 0/0 | 6209 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | copy fasta | chr6 | 41067974 | 41107403 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 33 | 3 | 12 | 7 | 5 | 6 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0002 | 0/0 | 28 | 1 | 9 | 9 | 3 | 6 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0003 | 0/0 | 8 | 0 | 2 | 2 | 0 | 4 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0004 | 0/0 | 24 | 0 | 0 | 24 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0006 | 0/0 | 8 | 1 | 1 | 6 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0007 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0008 | 0/0 | 5 | 1 | 1 | 2 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0023 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0002g0003 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0036 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0004g0005 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0005g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0006g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0007g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0008g0009 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0009g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0010g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0011g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0012g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0013g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0014g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0015g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0016g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0017g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0019g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0020g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0022g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0023g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0024g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0025g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0026g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0027g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0028g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0029g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0030g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0031g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0032g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0033g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0034g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0035g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0036g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0037g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0001t0038g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0001c0008t0018g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0002c0007t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0003c0006t0006g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
a0004c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00140 | hp1 | a0001 | c0001 | t0031 | g0088 | EUR | GBR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00280 | hp2 | a0001 | c0001 | t0032 | g0009 | EUR | FIN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00597 | hp1 | a0001 | c0001 | t0014 | g0008 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01069 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0009 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01243 | hp1 | a0001 | c0001 | t0029 | g0090 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0100 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01928 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02027 | hp1 | a0001 | c0001 | t0024 | g0002 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02040 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02129 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02273 | hp2 | a0001 | c0001 | t0008 | g0009 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02572 | hp2 | a0001 | c0001 | t0013 | g0113 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02615 | hp2 | a0001 | c0001 | t0011 | g0091 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02717 | hp1 | a0001 | c0008 | t0018 | g0093 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02809 | hp1 | a0001 | c0001 | t0017 | g0099 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02895 | hp2 | a0001 | c0001 | t0027 | g0121 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02896 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02897 | hp1 | a0001 | c0001 | t0010 | g0034 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0016 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02970 | hp1 | a0001 | c0001 | t0020 | g0101 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02970 | hp2 | a0001 | c0001 | t0035 | g0094 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03017 | hp1 | a0001 | c0001 | t0036 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03017 | hp2 | a0001 | c0005 | t0001 | g0084 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03098 | hp2 | a0002 | c0007 | t0007 | g0108 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03130 | hp1 | a0001 | c0001 | t0034 | g0026 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03139 | hp1 | a0001 | c0001 | t0011 | g0038 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03209 | hp2 | a0001 | c0001 | t0026 | g0104 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0016 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03486 | hp1 | a0001 | c0001 | t0028 | g0012 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03486 | hp2 | a0001 | c0001 | t0025 | g0057 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03491 | hp2 | a0001 | c0001 | t0023 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03669 | hp1 | a0001 | c0001 | t0037 | g0039 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03688 | hp2 | a0001 | c0001 | t0019 | g0006 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03942 | hp2 | a0001 | c0001 | t0021 | g0001 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | YRI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18940 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18960 | hp1 | a0001 | c0001 | t0016 | g0096 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18978 | hp1 | a0001 | c0001 | t0015 | g0021 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18979 | hp2 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | LWK | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0114 | AFR | LWK | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | LWK | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19060 | hp1 | a0001 | c0001 | t0038 | g0053 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19064 | hp2 | a0004 | c0004 | t0001 | g0079 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19067 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | YRI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | YRI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA20129 | hp2 | a0003 | c0006 | t0006 | g0011 | AFR | ASW | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA20905 | hp2 | a0001 | c0001 | t0015 | g0021 | SAS | GIH | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG06807 | hp1 | a0001 | c0001 | t0033 | g0103 | AFR | USA | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | USA | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA18955 | hp2 | a0001 | c0001 | t0014 | g0003 | EAS | JPT | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
NA20300 | hp2 | a0001 | c0001 | t0030 | g0064 | AFR | USA | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0023 | REF | REF | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0049 | REF | REF | NFYA_chr6_41067974_41107403 | NFYA | chr6 | 41067974 | 41107403 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41084186
|
G | T | 1 | a0002 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.303G>T | p.Leu101Phe | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/10 | 475/6209 | 303/1044 | 101/347 | chr6 | 41084186 | ||
chr6:41090211
|
A | C | 1 | a0003 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.449A>C | p.Gln150Pro | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/10 | 621/6209 | 449/1044 | 150/347 | chr6 | 41090211 | ||
chr6:41094491
|
T | G | 1 | a0004 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.984T>G | p.His328Gln | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/10 | 1156/6209 | 984/1044 | 328/347 | chr6 | 41094491 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41079131
|
G | A | 1 | a0001c0003 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.42G>A | p.Gln14Gln | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/10 | 214/6209 | 42/1044 | 14/347 | chr6 | 41079131 | ||
chr6:41080864
|
C | T | 1 | a0001c0008 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.129C>T | p.Ser43Ser | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/10 | 301/6209 | 129/1044 | 43/347 | chr6 | 41080864 | ||
chr6:41091619
|
C | T | 1 | a0001c0005 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.639C>T | p.Thr213Thr | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/10 | 811/6209 | 639/1044 | 213/347 | chr6 | 41091619 | ||
chr6:41092965
|
A | C | 1 | a0001c0002 | 5 | NA18941.hp1 NA18948.hp1 NA18978.hp2 others(2): Show |
synonymous_variant | LOW | c.768A>C | p.Gly256Gly | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/10 | 940/6209 | 768/1044 | 256/347 | chr6 | 41092965 | ||
chr6:41094401
|
C | T | 1 | a0001c0003 | 2 | HG02895.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.894C>T | p.Tyr298Tyr | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/10 | 1066/6209 | 894/1044 | 298/347 | chr6 | 41094401 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41097453
|
C | T | 1 | a0001c0001t0038 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 43 | chr6 | 41097453 | |||||
chr6:41097513
|
A | T | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*103A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 103 | chr6 | 41097513 | |||||
chr6:41097551
|
T | C | 2 | a0001c0001t0007a0002c0007t0007 | 5 | HG02280.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*141T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 141 | chr6 | 41097551 | |||||
chr6:41097558
|
T | C | 1 | a0001c0001t0016 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*148T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 148 | chr6 | 41097558 | |||||
chr6:41097673
|
A | G | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*263A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 263 | chr6 | 41097673 | |||||
chr6:41097685
|
C | A | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*275C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 275 | chr6 | 41097685 | |||||
chr6:41097842
|
A | C | 1 | a0001c0001t0036 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 432 | chr6 | 41097842 | |||||
chr6:41097919
|
C | T | 3 | a0001c0001t0014a0001c0001t0015a0001c0001t0037 | 5 | HG00597.hp1 HG03669.hp1 NA18955.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*509C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 509 | chr6 | 41097919 | |||||
chr6:41098073
|
A | G | 2 | a0001c0001t0013a0001c0001t0035 | 3 | HG02572.hp2 HG02970.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*663A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 663 | chr6 | 41098073 | |||||
chr6:41098479
|
G | A | 1 | a0001c0001t0017 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1069 | chr6 | 41098479 | |||||
chr6:41098523
|
A | G | 1 | a0001c0001t0034 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1113A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1113 | chr6 | 41098523 | |||||
chr6:41098559
|
A | G | 3 | a0001c0001t0006a0001c0001t0033a0003c0006t0006 | 7 | HG02572.hp1 HG03453.hp2 HG03471.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1149A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1149 | chr6 | 41098559 | |||||
chr6:41098685
|
G | A | 1 | a0001c0008t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1275G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1275 | chr6 | 41098685 | |||||
chr6:41098871
|
G | A | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1461G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1461 | chr6 | 41098871 | |||||
chr6:41098940
|
A | G | 1 | a0001c0001t0032 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1530A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1530 | chr6 | 41098940 | |||||
chr6:41099179
|
G | A | 1 | a0001c0001t0019 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 1769 | chr6 | 41099179 | |||||
chr6:41099583
|
A | T | 1 | a0001c0008t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2173A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2173 | chr6 | 41099583 | |||||
chr6:41099625
|
A | T | 1 | a0001c0001t0031 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2215A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2215 | chr6 | 41099625 | |||||
chr6:41099716
|
CT | C | 4 | a0001c0001t0005a0001c0001t0008a0001c0001t0020others(1): Show | 13 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2320delT | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2320 | INFO_REALIGN_3_PRIME | chr6 | 41099716 | ||||
chr6:41099807
|
C | G | 1 | a0001c0001t0030 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2397C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2397 | chr6 | 41099807 | |||||
chr6:41099943
|
T | C | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2533T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2533 | chr6 | 41099943 | |||||
chr6:41100045
|
T | A | 1 | a0001c0001t0021 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2635T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2635 | chr6 | 41100045 | |||||
chr6:41100053
|
G | A | 1 | a0001c0001t0022 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2643G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2643 | chr6 | 41100053 | |||||
chr6:41100270
|
C | T | 1 | a0001c0001t0012 | 2 | HG02040.hp1 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2860C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2860 | chr6 | 41100270 | |||||
chr6:41100318
|
G | T | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2908G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2908 | chr6 | 41100318 | |||||
chr6:41100402
|
A | G | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2992A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2992 | chr6 | 41100402 | |||||
chr6:41100409
|
C | T | 1 | a0001c0001t0028 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2999C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 2999 | chr6 | 41100409 | |||||
chr6:41100435
|
G | A | 1 | a0001c0001t0023 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3025G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3025 | chr6 | 41100435 | |||||
chr6:41100518
|
CA | C | 9 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(6): Show | 17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3110delA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3110 | INFO_REALIGN_3_PRIME | chr6 | 41100518 | ||||
chr6:41100594
|
G | A | 1 | a0001c0001t0037 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3184G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3184 | chr6 | 41100594 | |||||
chr6:41100684
|
G | T | 12 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(9): Show | 49 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3274G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3274 | chr6 | 41100684 | |||||
chr6:41100713
|
C | T | 1 | a0001c0001t0030 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3303C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3303 | chr6 | 41100713 | |||||
chr6:41100761
|
G | A | 8 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(5): Show | 16 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3351G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3351 | chr6 | 41100761 | |||||
chr6:41100768
|
C | G | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3358C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3358 | chr6 | 41100768 | |||||
chr6:41100769
|
C | G | 1 | a0001c0001t0025 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3359C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3359 | chr6 | 41100769 | |||||
chr6:41100802
|
G | T | 2 | a0001c0001t0008a0001c0001t0032 | 6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3392G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3392 | chr6 | 41100802 | |||||
chr6:41100820
|
A | T | 1 | a0001c0001t0035 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3410A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3410 | chr6 | 41100820 | |||||
chr6:41100841
|
G | C | 8 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(5): Show | 16 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3431G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3431 | chr6 | 41100841 | |||||
chr6:41100861
|
A | G | 9 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(6): Show | 17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3451A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3451 | chr6 | 41100861 | |||||
chr6:41100862
|
A | C | 9 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(6): Show | 17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3452A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3452 | chr6 | 41100862 | |||||
chr6:41100960
|
CCTGCTAG others(9): Show |
C | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3557_*3572delGGCG others(12): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3557 | INFO_REALIGN_3_PRIME | chr6 | 41100960 | ||||
chr6:41100967
|
G | T | 20 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(17): Show | 67 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*3557G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3557 | chr6 | 41100967 | |||||
chr6:41100972
|
A | C | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3562A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3562 | chr6 | 41100972 | |||||
chr6:41100972
|
A | G | 5 | a0001c0001t0004a0001c0001t0006a0001c0001t0026others(2): Show | 24 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3562A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3562 | chr6 | 41100972 | |||||
chr6:41101050
|
C | A | 7 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(4): Show | 16 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3640C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3640 | chr6 | 41101050 | |||||
chr6:41101256
|
G | T | 2 | a0001c0001t0008a0001c0001t0032 | 6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3846G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3846 | chr6 | 41101256 | |||||
chr6:41101316
|
C | T | 1 | a0001c0001t0027 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3906C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3906 | chr6 | 41101316 | |||||
chr6:41101381
|
G | A | 3 | a0001c0001t0002a0001c0001t0005a0001c0001t0038 | 32 | HG00609.hp1 HG02074.hp2 HG02129.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*3971G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3971 | chr6 | 41101381 | |||||
chr6:41101407
|
G | T | 2 | a0001c0001t0015a0001c0001t0037 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3997G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 3997 | chr6 | 41101407 | |||||
chr6:41101454
|
C | G | 9 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(6): Show | 17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4044C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4044 | chr6 | 41101454 | |||||
chr6:41101455
|
C | G | 9 | a0001c0001t0007a0001c0001t0008a0001c0001t0015others(6): Show | 17 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4045C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4045 | chr6 | 41101455 | |||||
chr6:41101551
|
A | G | 1 | a0001c0001t0026 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4141A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4141 | chr6 | 41101551 | |||||
chr6:41101799
|
G | C | 1 | a0001c0001t0029 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4389G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4389 | chr6 | 41101799 | |||||
chr6:41102060
|
G | A | 1 | a0001c0001t0024 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4650G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4650 | chr6 | 41102060 | |||||
chr6:41102316
|
T | G | 1 | a0001c0001t0010 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4906T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4906 | chr6 | 41102316 | |||||
chr6:41102369
|
T | G | 1 | a0001c0001t0017 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4959T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 10/10 | 4959 | chr6 | 41102369 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41073222
|
G | A | 1 | a0001c0001t0011g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-62+138G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073222 | ||||||
chr6:41073223
|
C | G | 1 | a0001c0001t0011g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-62+139C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073223 | ||||||
chr6:41073239
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-62+155G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073239 | ||||||
chr6:41073269
|
G | A | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-62+185G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073269 | ||||||
chr6:41073284
|
G | C | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+200G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073284 | ||||||
chr6:41073320
|
G | C | 3 | a0001c0001t0004g0012a0001c0001t0004g0040a0001c0001t0028g0012 | 5 | HG02258.hp1 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-62+236G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073320 | ||||||
chr6:41073435
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-62+351A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073435 | ||||||
chr6:41073491
|
C | T | 1 | a0001c0001t0003g0020 | 3 | HG02559.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-62+407C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073491 | ||||||
chr6:41073622
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0017others(8): Show | 23 | HG00558.hp2 HG01891.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-62+538G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073622 | ||||||
chr6:41073763
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-62+679C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073763 | ||||||
chr6:41073810
|
C | T | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-62+726C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073810 | ||||||
chr6:41073924
|
T | TCTCCGTT others(418): Show |
1 | a0001c0001t0001g0022 | 2 | HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-62+852_-62+853ins others(425): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 41073924 | |||||
chr6:41073939
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-62+855C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41073939 | ||||||
chr6:41074003
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(60): Show | 154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-62+919C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074003 | ||||||
chr6:41074013
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(60): Show | 154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-62+929G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074013 | ||||||
chr6:41074090
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(62): Show | 157 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.-62+1006A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074090 | ||||||
chr6:41074107
|
G | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0119 | 6 | HG00558.hp2 NA18970.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62+1023G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074107 | ||||||
chr6:41074108
|
T | G | 1 | a0001c0001t0001g0018 | 3 | HG03927.hp2 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-62+1024T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074108 | ||||||
chr6:41074208
|
T | A | 2 | a0001c0001t0008g0009a0001c0001t0032g0009 | 6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.-62+1124T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074208 | ||||||
chr6:41074491
|
A | T | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-62+1407A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074491 | ||||||
chr6:41074652
|
T | A | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+1568T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074652 | ||||||
chr6:41074773
|
T | G | 1 | a0001c0001t0001g0048 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-62+1689T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074773 | ||||||
chr6:41074811
|
A | T | 1 | a0001c0001t0031g0088 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-62+1727A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074811 | ||||||
chr6:41074851
|
T | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(60): Show | 154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-62+1767T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41074851 | ||||||
chr6:41075254
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(62): Show | 157 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.-62+2170G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075254 | ||||||
chr6:41075261
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-62+2177A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075261 | ||||||
chr6:41075301
|
T | C | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+2217T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075301 | ||||||
chr6:41075409
|
T | A | 1 | a0001c0001t0001g0023 | 2 | HG01496.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-62+2325T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075409 | ||||||
chr6:41075464
|
T | C | 1 | a0001c0001t0001g0031 | 2 | HG00639.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.-62+2380T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075464 | ||||||
chr6:41075475
|
A | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0037others(4): Show | 33 | HG02523.hp1 NA18747.hp1 NA18948.hp2 others(30): Show |
intron_variant | MODIFIER | c.-62+2391A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075475 | ||||||
chr6:41075510
|
C | A | 1 | a0001c0001t0001g0024 | 2 | NA18960.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-62+2426C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075510 | ||||||
chr6:41075595
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-62+2511G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075595 | ||||||
chr6:41075726
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(60): Show | 154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-62+2642G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075726 | ||||||
chr6:41075733
|
C | CT | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-62+2660dupT | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 41075733 | |||||
chr6:41075805
|
T | G | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-62+2721T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075805 | ||||||
chr6:41075837
|
G | C | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+2753G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075837 | ||||||
chr6:41075929
|
T | A | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-62+2845T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41075929 | ||||||
chr6:41076037
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-62+2953C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076037 | ||||||
chr6:41076155
|
C | A | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-61-2874C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076155 | ||||||
chr6:41076244
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-61-2785A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076244 | ||||||
chr6:41076332
|
A | G | 2 | a0001c0001t0013g0113a0001c0001t0013g0114 | 2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-61-2697A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076332 | ||||||
chr6:41076445
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-61-2584C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076445 | ||||||
chr6:41076841
|
T | C | 1 | a0001c0001t0002g0051 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-61-2188T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41076841 | ||||||
chr6:41077218
|
A | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(60): Show | 154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-61-1811A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077218 | ||||||
chr6:41077236
|
G | A | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-61-1793G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077236 | ||||||
chr6:41077247
|
A | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(62): Show | 157 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(154): Show |
intron_variant | MODIFIER | c.-61-1782A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077247 | ||||||
chr6:41077531
|
T | C | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(60): Show | 154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-61-1498T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077531 | ||||||
chr6:41077540
|
ATGTAT | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(51): Show | 139 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.-61-1485_-61-1481d others(7): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr6 | 41077540 | |||||
chr6:41077827
|
C | G | 4 | a0001c0001t0003g0020a0001c0001t0003g0036a0001c0001t0003g0111others(1): Show | 7 | HG02559.hp2 HG02622.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-61-1202C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41077827 | ||||||
chr6:41078438
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(60): Show | 154 | HG00099.hp1 HG00280.hp2 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.-61-591G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41078438 | ||||||
chr6:41078480
|
CTT | C | 55 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(52): Show | 140 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.-61-548_-61-547del others(2): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41078480 | ||||||
chr6:41078666
|
A | C | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-61-363A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41078666 | ||||||
chr6:41078910
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-61-119C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 1/9 | chr6 | 41078910 | ||||||
chr6:41079283
|
G | A | 4 | a0001c0001t0008g0009a0001c0001t0011g0038a0001c0001t0011g0091others(1): Show | 8 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+119G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41079283 | ||||||
chr6:41079588
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.75+424C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41079588 | ||||||
chr6:41079639
|
T | C | 3 | a0001c0001t0013g0113a0001c0001t0013g0114a0001c0001t0035g0094 | 3 | HG02572.hp2 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.75+475T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41079639 | ||||||
chr6:41079800
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.75+636A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41079800 | ||||||
chr6:41080053
|
G | C | 1 | a0001c0001t0003g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.76-758G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080053 | ||||||
chr6:41080326
|
G | A | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.76-485G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080326 | ||||||
chr6:41080386
|
C | T | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.76-425C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080386 | ||||||
chr6:41080505
|
C | T | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.76-306C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080505 | ||||||
chr6:41080718
|
C | T | 2 | a0001c0001t0013g0113a0001c0001t0013g0114 | 2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.76-93C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 2/9 | chr6 | 41080718 | ||||||
chr6:41081125
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.162+228T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081125 | ||||||
chr6:41081155
|
A | G | 1 | a0001c0005t0001g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.162+258A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081155 | ||||||
chr6:41081218
|
G | A | 30 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(27): Show | 89 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.162+321G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081218 | ||||||
chr6:41081264
|
C | T | 1 | a0001c0001t0003g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.162+367C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081264 | ||||||
chr6:41081406
|
C | T | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+509C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081406 | ||||||
chr6:41081415
|
A | G | 2 | a0001c0001t0011g0038a0001c0001t0011g0091 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.162+518A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081415 | ||||||
chr6:41081418
|
A | G | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+521A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081418 | ||||||
chr6:41081429
|
G | T | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.162+532G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081429 | ||||||
chr6:41081447
|
G | A | 1 | a0001c0001t0038g0053 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.162+550G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081447 | ||||||
chr6:41081501
|
A | C | 1 | a0001c0001t0010g0034 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.162+604A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081501 | ||||||
chr6:41081571
|
C | T | 7 | a0001c0001t0008g0009a0001c0001t0011g0038a0001c0001t0011g0091others(4): Show | 12 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+674C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081571 | ||||||
chr6:41081700
|
ATCTTGTT others(4): Show |
A | 2 | a0001c0001t0001g0092a0001c0008t0018g0093 | 2 | HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.162+813_162+823del others(11): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 41081700 | |||||
chr6:41081769
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(23): Show | 85 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.162+872T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081769 | ||||||
chr6:41081903
|
G | GGCTAA | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+1008_162+1012d others(7): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 41081903 | |||||
chr6:41081952
|
C | T | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+1055C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081952 | ||||||
chr6:41081961
|
C | G | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.162+1064C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41081961 | ||||||
chr6:41082148
|
A | G | 2 | a0001c0001t0011g0091a0001c0008t0018g0093 | 2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.162+1251A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082148 | ||||||
chr6:41082156
|
T | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(49): Show | 137 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.162+1259T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082156 | ||||||
chr6:41082202
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.162+1305A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082202 | ||||||
chr6:41082300
|
T | C | 1 | a0001c0001t0025g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.162+1403T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082300 | ||||||
chr6:41082541
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.163-1505A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082541 | ||||||
chr6:41082760
|
T | C | 1 | a0001c0001t0003g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.163-1286T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082760 | ||||||
chr6:41082982
|
C | T | 5 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0009g0016others(2): Show | 11 | HG00558.hp2 HG02896.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.163-1064C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41082982 | ||||||
chr6:41083132
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.163-914A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083132 | ||||||
chr6:41083348
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.163-698A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083348 | ||||||
chr6:41083362
|
A | G | 1 | a0001c0001t0003g0033 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.163-684A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083362 | ||||||
chr6:41083381
|
G | A | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.163-665G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083381 | ||||||
chr6:41083483
|
G | GTA | 15 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0017others(12): Show | 28 | HG00558.hp2 HG01891.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.163-560_163-559dup others(2): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr6 | 41083483 | |||||
chr6:41083687
|
C | A | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.163-359C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083687 | ||||||
chr6:41083813
|
A | G | 1 | a0001c0008t0018g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.163-233A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41083813 | ||||||
chr6:41084001
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.163-45T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 3/9 | chr6 | 41084001 | ||||||
chr6:41084263
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.309+71A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084263 | ||||||
chr6:41084341
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.309+149A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084341 | ||||||
chr6:41084375
|
A | C | 1 | a0001c0001t0001g0029 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.309+183A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084375 | ||||||
chr6:41084458
|
A | G | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.309+266A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084458 | ||||||
chr6:41084485
|
G | A | 3 | a0001c0001t0015g0021a0001c0001t0029g0090a0001c0001t0037g0039 | 4 | HG01243.hp1 HG03669.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.309+293G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084485 | ||||||
chr6:41084804
|
A | C | 1 | a0001c0001t0003g0112 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.309+612A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084804 | ||||||
chr6:41084822
|
C | G | 2 | a0001c0001t0004g0005a0001c0001t0004g0107 | 11 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.309+630C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084822 | ||||||
chr6:41084989
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.309+797T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41084989 | ||||||
chr6:41085130
|
A | G | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.309+938A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085130 | ||||||
chr6:41085135
|
A | C | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.309+943A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085135 | ||||||
chr6:41085476
|
C | G | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.309+1284C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085476 | ||||||
chr6:41085682
|
G | A | 1 | a0001c0001t0003g0033 | 2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.309+1490G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085682 | ||||||
chr6:41085752
|
AT | A | 38 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(35): Show | 73 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.309+1572delT | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41085752 | |||||
chr6:41085784
|
G | A | 11 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(8): Show | 20 | HG01175.hp2 HG02257.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.309+1592G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085784 | ||||||
chr6:41085829
|
G | C | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.309+1637G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41085829 | ||||||
chr6:41086206
|
CA | C | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.309+2016delA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41086206 | |||||
chr6:41086522
|
G | GT | 18 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0058others(15): Show | 46 | HG00280.hp1 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.309+2338dupT | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41086522 | |||||
chr6:41086549
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.309+2357C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41086549 | ||||||
chr6:41086671
|
A | G | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.309+2479A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41086671 | ||||||
chr6:41086734
|
A | G | 1 | a0001c0001t0003g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.309+2542A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41086734 | ||||||
chr6:41086740
|
T | A | 1 | a0001c0001t0003g0109 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.309+2548T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41086740 | ||||||
chr6:41087172
|
A | G | 1 | a0001c0001t0001g0028 | 2 | HG02630.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.310-2407A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087172 | ||||||
chr6:41087252
|
G | C | 2 | a0001c0001t0011g0038a0001c0001t0011g0091 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.310-2327G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087252 | ||||||
chr6:41087465
|
A | T | 2 | a0001c0001t0013g0113a0001c0001t0013g0114 | 2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.310-2114A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087465 | ||||||
chr6:41087475
|
A | G | 1 | a0001c0001t0001g0027 | 2 | HG01081.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.310-2104A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087475 | ||||||
chr6:41087555
|
A | G | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-2024A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087555 | ||||||
chr6:41087716
|
T | TA | 2 | a0001c0001t0008g0009a0001c0001t0032g0009 | 6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-1853dupA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41087716 | |||||
chr6:41087733
|
A | G | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.310-1846A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087733 | ||||||
chr6:41087880
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.310-1699A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087880 | ||||||
chr6:41087889
|
G | T | 2 | a0001c0001t0008g0009a0001c0001t0032g0009 | 6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-1690G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41087889 | ||||||
chr6:41088142
|
G | A | 27 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(24): Show | 50 | HG01175.hp2 HG01255.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.310-1437G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088142 | ||||||
chr6:41088183
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.310-1396C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088183 | ||||||
chr6:41088189
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.310-1390C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088189 | ||||||
chr6:41088217
|
G | A | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.310-1362G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088217 | ||||||
chr6:41088423
|
C | CA | 13 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0031others(10): Show | 20 | HG00597.hp1 HG00639.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.310-1134dupA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | |||||
chr6:41088423
|
C | CAA | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0115others(6): Show | 11 | HG01175.hp1 HG01243.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.310-1135_310-1134d others(4): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | |||||
chr6:41088423
|
C | CAAA | 17 | a0001c0001t0003g0010a0001c0001t0003g0033a0001c0001t0003g0102others(14): Show | 37 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.310-1136_310-1134d others(5): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | |||||
chr6:41088423
|
C | CAAAA | 10 | a0001c0001t0003g0020a0001c0001t0003g0036a0001c0001t0003g0111others(7): Show | 20 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.310-1137_310-1134d others(6): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | |||||
chr6:41088423
|
CA | C | 7 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0070others(4): Show | 8 | HG00558.hp1 HG01261.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.310-1134delA | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr6 | 41088423 | |||||
chr6:41088446
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.310-1133T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088446 | ||||||
chr6:41088504
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.310-1075A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088504 | ||||||
chr6:41088610
|
T | C | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-969T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088610 | ||||||
chr6:41088766
|
A | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0017others(10): Show | 25 | HG00558.hp2 HG02074.hp1 HG02132.hp2 others(22): Show |
intron_variant | MODIFIER | c.310-813A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088766 | ||||||
chr6:41088953
|
A | G | 2 | a0001c0001t0007g0015a0002c0007t0007g0108 | 5 | HG02280.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.310-626A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088953 | ||||||
chr6:41088988
|
A | G | 1 | a0001c0001t0037g0039 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.310-591A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41088988 | ||||||
chr6:41089047
|
G | A | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-532G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41089047 | ||||||
chr6:41089377
|
T | C | 1 | a0001c0001t0001g0037 | 2 | NA18956.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.310-202T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41089377 | ||||||
chr6:41089398
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.310-181C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41089398 | ||||||
chr6:41089555
|
C | G | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-24C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 4/9 | chr6 | 41089555 | ||||||
chr6:41089809
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.441+99G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 5/9 | chr6 | 41089809 | ||||||
chr6:41089886
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.441+176G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 5/9 | chr6 | 41089886 | ||||||
chr6:41090066
|
C | T | 2 | a0001c0001t0007g0015a0002c0007t0007g0108 | 5 | HG02280.hp2 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.442-138C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 5/9 | chr6 | 41090066 | ||||||
chr6:41090578
|
A | T | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.547+269A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090578 | ||||||
chr6:41090598
|
G | A | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.547+289G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090598 | ||||||
chr6:41090688
|
G | T | 1 | a0001c0001t0004g0106 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.547+379G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090688 | ||||||
chr6:41090691
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.547+382T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090691 | ||||||
chr6:41090692
|
A | C | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.547+383A>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090692 | ||||||
chr6:41090751
|
A | G | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.547+442A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090751 | ||||||
chr6:41090850
|
A | G | 1 | a0001c0001t0026g0104 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.547+541A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41090850 | ||||||
chr6:41091045
|
C | G | 1 | a0001c0008t0018g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.548-483C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091045 | ||||||
chr6:41091076
|
A | G | 1 | a0001c0001t0017g0099 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.548-452A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091076 | ||||||
chr6:41091174
|
A | T | 37 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(34): Show | 69 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.548-354A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091174 | ||||||
chr6:41091229
|
G | A | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.548-299G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091229 | ||||||
chr6:41091287
|
G | C | 1 | a0001c0008t0018g0093 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.548-241G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091287 | ||||||
chr6:41091430
|
G | A | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.548-98G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 6/9 | chr6 | 41091430 | ||||||
chr6:41091719
|
T | G | 37 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(34): Show | 69 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.714+25T>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091719 | ||||||
chr6:41091752
|
T | C | 1 | a0001c0001t0009g0016 | 3 | HG02896.hp2 HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.714+58T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091752 | ||||||
chr6:41091791
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.714+97G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091791 | ||||||
chr6:41091846
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.714+152C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091846 | ||||||
chr6:41091871
|
A | G | 24 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(21): Show | 83 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.714+177A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091871 | ||||||
chr6:41091900
|
T | C | 1 | a0001c0001t0016g0096 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.714+206T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091900 | ||||||
chr6:41091969
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.714+275C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41091969 | ||||||
chr6:41092134
|
C | T | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.714+440C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092134 | ||||||
chr6:41092184
|
TAAGAATG others(6): Show |
T | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.714+492_714+504del others(13): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr6 | 41092184 | |||||
chr6:41092199
|
G | T | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.714+505G>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092199 | ||||||
chr6:41092200
|
A | T | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.714+506A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092200 | ||||||
chr6:41092233
|
G | A | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.714+539G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092233 | ||||||
chr6:41092277
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.714+583A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092277 | ||||||
chr6:41092473
|
C | G | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.715-439C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092473 | ||||||
chr6:41092540
|
T | C | 5 | a0001c0001t0003g0100a0001c0001t0013g0113a0001c0001t0013g0114others(2): Show | 5 | HG01255.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-372T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092540 | ||||||
chr6:41092552
|
T | C | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.715-360T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092552 | ||||||
chr6:41092776
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.715-136T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 7/9 | chr6 | 41092776 | ||||||
chr6:41093220
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.888+135G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093220 | ||||||
chr6:41093362
|
T | C | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.888+277T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093362 | ||||||
chr6:41093369
|
G | A | 1 | a0001c0001t0001g0018 | 3 | HG03927.hp2 HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.888+284G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093369 | ||||||
chr6:41093415
|
A | G | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.888+330A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093415 | ||||||
chr6:41093457
|
G | C | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.888+372G>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093457 | ||||||
chr6:41093478
|
T | A | 1 | a0001c0003t0001g0030 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.888+393T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093478 | ||||||
chr6:41093564
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.888+479A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093564 | ||||||
chr6:41093628
|
G | A | 1 | a0001c0001t0011g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.888+543G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093628 | ||||||
chr6:41093690
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.888+605C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093690 | ||||||
chr6:41093751
|
G | A | 1 | a0001c0001t0016g0096 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.889-645G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093751 | ||||||
chr6:41093766
|
C | T | 1 | a0001c0001t0025g0057 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.889-630C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093766 | ||||||
chr6:41093809
|
G | A | 27 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(24): Show | 50 | HG01175.hp2 HG01255.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.889-587G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093809 | ||||||
chr6:41093854
|
T | C | 27 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(24): Show | 50 | HG01175.hp2 HG01255.hp2 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.889-542T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41093854 | ||||||
chr6:41094009
|
T | C | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.889-387T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094009 | ||||||
chr6:41094090
|
G | A | 1 | a0001c0001t0027g0121 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.889-306G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094090 | ||||||
chr6:41094143
|
G | GTC | 3 | a0001c0001t0004g0012a0001c0001t0004g0040a0001c0001t0028g0012 | 5 | HG02258.hp1 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.889-252_889-251ins others(2): Show |
NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | 41094143 | |||||
chr6:41094164
|
T | A | 3 | a0001c0001t0011g0038a0001c0001t0011g0091a0001c0001t0013g0113 | 3 | HG02572.hp2 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.889-232T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094164 | ||||||
chr6:41094165
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.889-231A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094165 | ||||||
chr6:41094266
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.889-130T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 8/9 | chr6 | 41094266 | ||||||
chr6:41094624
|
A | G | 1 | a0001c0001t0029g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.990+127A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41094624 | ||||||
chr6:41094950
|
C | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0018others(23): Show | 86 | HG00099.hp1 HG00609.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.990+453C>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41094950 | ||||||
chr6:41095326
|
C | T | 39 | a0001c0001t0003g0010a0001c0001t0003g0020a0001c0001t0003g0033others(36): Show | 72 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.990+829C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095326 | ||||||
chr6:41095392
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.990+895T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095392 | ||||||
chr6:41095678
|
G | A | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.990+1181G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095678 | ||||||
chr6:41095710
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.990+1213C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095710 | ||||||
chr6:41095711
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.990+1214G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095711 | ||||||
chr6:41095767
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.990+1270A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41095767 | ||||||
chr6:41096188
|
T | A | 2 | a0001c0001t0011g0038a0001c0001t0011g0091 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.991-1169T>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096188 | ||||||
chr6:41096244
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.991-1113C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096244 | ||||||
chr6:41096281
|
A | G | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.991-1076A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096281 | ||||||
chr6:41096741
|
C | T | 2 | a0001c0001t0015g0021a0001c0001t0037g0039 | 3 | HG03669.hp1 NA18978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.991-616C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096741 | ||||||
chr6:41096787
|
A | T | 1 | a0001c0001t0001g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.991-570A>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096787 | ||||||
chr6:41096907
|
C | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0075a0001c0001t0030g0064 | 3 | HG01981.hp2 HG03834.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.991-450C>T | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096907 | ||||||
chr6:41096954
|
T | C | 1 | a0001c0001t0001g0025 | 2 | NA19063.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.991-403T>C | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41096954 | ||||||
chr6:41097067
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0089 | 3 | HG01099.hp1 HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.991-290G>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41097067 | ||||||
chr6:41097114
|
C | A | 2 | a0001c0001t0008g0009a0001c0001t0032g0009 | 6 | HG00280.hp2 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.991-243C>A | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41097114 | ||||||
chr6:41097300
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.991-57A>G | NFYA | ENSG00000001167.15 | transcript | ENST00000341376.11 | protein_coding | 9/9 | chr6 | 41097300 |