Item | Value |
---|---|
geneid | 80854 |
ensemblid | ENSG00000145391.14 |
hgncid | 30412 |
symbol | SETD7 |
name | SET domain containing 7, histone lysine methyltransferase |
refseq_nuc | NM_030648.4 |
refseq_prot | NP_085151.1 |
ensembl_nuc | ENST00000274031.8 |
ensembl_prot | ENSP00000274031.3 |
mane_status | MANE Select |
chr | chr4 |
start | 139506038 |
end | 139556219 |
strand | - |
ver | v1.2 |
region | chr4:139506038-139556219 |
region5000 | chr4:139501038-139561219 |
regionname0 | SETD7_chr4_139506038_139556219 |
regionname5000 | SETD7_chr4_139501038_139561219 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 366 | 313 | 95 | 60 | 104 | 17 | 36 | 66 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0002 | 0/1 | 366 | 3 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1101 | 298 | 89 | 57 | 99 | 17 | 35 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
c0002 | 0/0 | 1101 | 8 | 1 | 3 | 4 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
c0003 | 0/1 | 1101 | 3 | 1 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
c0004 | 0/0 | 1101 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
c0005 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
c0006 | 0/0 | 1101 | 2 | 0 | 0 | 1 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 5692 | 197 | 32 | 44 | 88 | 11 | 21 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0002 | 0/0 | 5708 | 16 | 1 | 6 | 0 | 1 | 8 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0003 | 0/0 | 5692 | 9 | 9 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0004 | 0/0 | 5708 | 7 | 7 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0005 | 0/0 | 5708 | 6 | 5 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0006 | 0/0 | 5708 | 5 | 0 | 2 | 0 | 2 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0007 | 0/0 | 5708 | 4 | 4 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0008 | 0/0 | 5692 | 3 | 0 | 0 | 3 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0009 | 0/0 | 5692 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0010 | 0/0 | 5708 | 3 | 1 | 1 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0011 | 0/0 | 5708 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0012 | 0/0 | 5708 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0013 | 0/0 | 5708 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0014 | 0/0 | 5708 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0015 | 0/0 | 5708 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0016 | 0/0 | 5692 | 2 | 0 | 0 | 0 | 2 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0017 | 0/0 | 5692 | 2 | 1 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0018 | 0/0 | 5692 | 2 | 0 | 0 | 1 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0019 | 0/0 | 5692 | 2 | 0 | 0 | 0 | 1 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0020 | 0/0 | 5708 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0021 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0022 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0023 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0024 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0025 | 1/0 | 5708 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0026 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0027 | 0/0 | 5708 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0028 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0029 | 0/0 | 5708 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0030 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0031 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0032 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0033 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0034 | 0/0 | 5692 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0035 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0036 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0037 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0038 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0039 | 0/0 | 5692 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0040 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0041 | 0/0 | 5692 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0042 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0043 | 0/0 | 5692 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0044 | 0/0 | 5692 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0045 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0046 | 0/0 | 5692 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0047 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0048 | 0/0 | 5692 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0049 | 0/0 | 5708 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0050 | 0/0 | 5692 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0051 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0052 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0053 | 0/0 | 5708 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0054 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0055 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0056 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0057 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0058 | 0/0 | 5708 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0059 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
t0060 | 0/0 | 5692 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0002 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1101 | 298 | 89 | 57 | 99 | 17 | 35 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
a0001c0002 | 0/0 | 1101 | 8 | 1 | 3 | 4 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
a0001c0004 | 0/0 | 1101 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
a0001c0005 | 0/0 | 1101 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
a0001c0006 | 0/0 | 1101 | 2 | 0 | 0 | 1 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 | |
a0002c0003 | 0/1 | 1101 | 3 | 1 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6792 | 190 | 30 | 44 | 85 | 10 | 21 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0002 | 0/0 | 6808 | 16 | 1 | 6 | 0 | 1 | 8 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0003 | 0/0 | 6792 | 9 | 9 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0004 | 0/0 | 6808 | 7 | 7 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0005 | 0/0 | 6808 | 6 | 5 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0006 | 0/0 | 6808 | 3 | 0 | 0 | 0 | 2 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0007 | 0/0 | 6808 | 4 | 4 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0008 | 0/0 | 6792 | 3 | 0 | 0 | 3 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0009 | 0/0 | 6792 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0011 | 0/0 | 6808 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0012 | 0/0 | 6808 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0013 | 0/0 | 6808 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0014 | 0/0 | 6808 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0015 | 0/0 | 6808 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0016 | 0/0 | 6792 | 2 | 0 | 0 | 0 | 2 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0017 | 0/0 | 6792 | 2 | 1 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0018 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0019 | 0/0 | 6792 | 2 | 0 | 0 | 0 | 1 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0020 | 0/0 | 6808 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0021 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0022 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0023 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0024 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0025 | 1/0 | 6808 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0026 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0027 | 0/0 | 6808 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0028 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0029 | 0/0 | 6808 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0030 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0031 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0032 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0034 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0035 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0036 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0037 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0038 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0039 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0040 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0041 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0042 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0043 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0044 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0046 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0047 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0048 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0049 | 0/0 | 6808 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0050 | 0/0 | 6792 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0051 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0052 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0053 | 0/0 | 6808 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0055 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0056 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0057 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0059 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0001t0060 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0002t0001 | 0/0 | 6792 | 3 | 0 | 0 | 3 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0002t0006 | 0/0 | 6808 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0002t0010 | 0/0 | 6808 | 3 | 1 | 1 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0004t0001 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0004t0012 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0004t0033 | 0/0 | 6792 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0005t0054 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0005t0058 | 0/0 | 6808 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0006t0018 | 0/0 | 6792 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0001c0006t0045 | 0/0 | 6792 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
a0002c0003t0001 | 0/1 | 6792 | 3 | 1 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | copy fasta | chr4 | 139501038 | 139561219 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0006g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0008g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0008g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0011g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0012g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0012g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0013g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0013g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0014g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0014g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0015g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0016g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0016g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0017g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0017g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0018g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0019g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0019g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0020g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0020g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0021g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0022g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0023g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0024g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0025g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0026g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0027g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0028g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0029g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0030g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0031g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0032g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0034g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0035g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0036g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0037g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0038g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0039g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0040g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0041g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0042g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0043g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0044g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0046g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0047g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0048g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0049g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0050g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0051g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0052g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0053g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0055g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0056g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0057g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0059g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0001t0060g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0002t0010g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0004t0012g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0004t0033g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0005t0054g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0005t0058g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0006t0018g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0001c0006t0045g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0002c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
a0002c0003t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0053 | EUR | GBR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00099 | hp2 | a0002 | c0003 | t0001 | g0047 | EUR | GBR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | FIN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | FIN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00323 | hp2 | a0001 | c0001 | t0019 | g0106 | EUR | FIN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00423 | hp2 | a0001 | c0001 | t0018 | g0084 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00438 | hp1 | a0001 | c0006 | t0045 | g0266 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00642 | hp2 | a0001 | c0002 | t0006 | g0135 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG00741 | hp2 | a0001 | c0001 | t0044 | g0048 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01074 | hp1 | a0001 | c0001 | t0048 | g0087 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01074 | hp2 | a0001 | c0002 | t0006 | g0136 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01106 | hp2 | a0001 | c0001 | t0017 | g0033 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01192 | hp1 | a0001 | c0001 | t0053 | g0284 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0062 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0278 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01496 | hp1 | a0001 | c0001 | t0049 | g0236 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0005 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01516 | hp2 | a0001 | c0001 | t0016 | g0262 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0005 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01517 | hp2 | a0001 | c0001 | t0016 | g0264 | EUR | IBS | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01884 | hp2 | a0001 | c0001 | t0026 | g0034 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01978 | hp1 | a0001 | c0001 | t0050 | g0206 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02040 | hp1 | a0001 | c0001 | t0008 | g0025 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02055 | hp2 | a0001 | c0001 | t0031 | g0227 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02145 | hp2 | a0001 | c0001 | t0013 | g0057 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02148 | hp2 | a0001 | c0002 | t0010 | g0265 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CDX | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CDX | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02257 | hp1 | a0001 | c0001 | t0040 | g0288 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0121 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0230 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0239 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02572 | hp1 | a0001 | c0001 | t0017 | g0027 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02572 | hp2 | a0001 | c0001 | t0038 | g0222 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02717 | hp1 | a0001 | c0004 | t0012 | g0251 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02809 | hp1 | a0001 | c0001 | t0013 | g0006 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0242 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02818 | hp1 | a0001 | c0001 | t0057 | g0229 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02886 | hp1 | a0001 | c0001 | t0032 | g0086 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02896 | hp1 | a0001 | c0001 | t0013 | g0006 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02965 | hp1 | a0001 | c0001 | t0024 | g0134 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02965 | hp2 | a0001 | c0005 | t0058 | g0282 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0145 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03017 | hp1 | a0001 | c0001 | t0034 | g0226 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03017 | hp2 | a0001 | c0001 | t0019 | g0050 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03041 | hp2 | a0001 | c0005 | t0054 | g0283 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03098 | hp1 | a0001 | c0002 | t0010 | g0176 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0279 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0252 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03195 | hp1 | a0001 | c0001 | t0052 | g0042 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0125 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03225 | hp1 | a0001 | c0001 | t0014 | g0180 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03225 | hp2 | a0001 | c0001 | t0055 | g0232 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03453 | hp2 | a0001 | c0001 | t0030 | g0245 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03486 | hp1 | a0001 | c0001 | t0014 | g0056 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03486 | hp2 | a0001 | c0001 | t0035 | g0022 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03491 | hp1 | a0001 | c0006 | t0018 | g0067 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03516 | hp1 | a0001 | c0004 | t0033 | g0071 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03516 | hp2 | a0001 | c0001 | t0020 | g0238 | AFR | ESN | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0188 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03710 | hp2 | a0001 | c0001 | t0043 | g0256 | SAS | PJL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03834 | hp1 | a0001 | c0001 | t0029 | g0190 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0030 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04199 | hp2 | a0001 | c0001 | t0041 | g0214 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0122 | SAS | STU | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18906 | hp1 | a0001 | c0001 | t0051 | g0144 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18947 | hp1 | a0001 | c0001 | t0023 | g0235 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18964 | hp2 | a0001 | c0001 | t0008 | g0269 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18971 | hp2 | a0001 | c0002 | t0010 | g0208 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18974 | hp1 | a0001 | c0001 | t0036 | g0109 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18977 | hp1 | a0001 | c0001 | t0021 | g0080 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18983 | hp2 | a0001 | c0001 | t0008 | g0268 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18986 | hp1 | a0001 | c0001 | t0022 | g0270 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18986 | hp2 | a0001 | c0001 | t0060 | g0291 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18997 | hp1 | a0001 | c0001 | t0037 | g0105 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18997 | hp2 | a0001 | c0001 | t0047 | g0192 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19009 | hp2 | a0001 | c0001 | t0027 | g0049 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19012 | hp2 | a0001 | c0001 | t0059 | g0111 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0178 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19030 | hp2 | a0001 | c0001 | t0056 | g0031 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0177 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19056 | hp1 | a0001 | c0001 | t0042 | g0099 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20129 | hp1 | a0001 | c0001 | t0015 | g0212 | AFR | ASW | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | TSI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | TSI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20805 | hp2 | a0001 | c0001 | t0039 | g0257 | EUR | TSI | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02486 | hp1 | a0001 | c0001 | t0028 | g0215 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02559 | hp1 | a0001 | c0001 | t0011 | g0189 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG02559 | hp2 | a0001 | c0001 | t0046 | g0289 | AFR | ACB | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | USA | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
HG06807 | hp2 | a0001 | c0001 | t0020 | g0020 | AFR | USA | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | USA | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA20300 | hp2 | a0001 | c0001 | t0012 | g0228 | AFR | USA | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | LWK | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0001 | g0124 | REF | REF | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0025 | g0108 | REF | REF | SETD7_chr4_139501038_139561219 | SETD7 | chr4 | 139501038 | 139561219 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139523358 | C | T | 1 | a0002 | 3 | HG00099.hp2 HG02257.hp2 homoSapiens_chm13v2.hp1 |
missense_variant | MODERATE | c.640G>A | p.Glu214Lys | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/8 | 722/6808 | 640/1101 | 214/366 | chr4 | 139523358 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139529050 | G | A | 1 | a0001c0006 | 2 | HG00438.hp1 HG03491.hp1 |
synonymous_variant | LOW | c.543C>T | p.His181His | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/8 | 625/6808 | 543/1101 | 181/366 | chr4 | 139529050 | ||
chr4:139529155 | A | G | 1 | a0001c0002 | 8 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(5): Show |
synonymous_variant | LOW | c.438T>C | p.Tyr146Tyr | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/8 | 520/6808 | 438/1101 | 146/366 | chr4 | 139529155 | ||
chr4:139533261 | G | A | 1 | a0001c0004 | 3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.276C>T | p.Asn92Asn | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/8 | 358/6808 | 276/1101 | 92/366 | chr4 | 139533261 | ||
chr4:139547024 | C | T | 1 | a0001c0005 | 2 | HG02965.hp2 HG03041.hp2 |
synonymous_variant | LOW | c.66G>A | p.Pro22Pro | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/8 | 148/6808 | 66/1101 | 22/366 | chr4 | 139547024 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139506341 | G | A | 2 | a0001c0001t0003a0001c0001t0005 | 15 | HG01361.hp1 HG01884.hp1 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5322C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 5322 | chr4 | 139506341 | |||||
chr4:139506483 | G | A | 1 | a0001c0001t0052 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5180C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 5180 | chr4 | 139506483 | |||||
chr4:139506495 | C | G | 1 | a0001c0001t0029 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5168G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 5168 | chr4 | 139506495 | |||||
chr4:139506603 | A | G | 1 | a0001c0001t0040 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5060T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 5060 | chr4 | 139506603 | |||||
chr4:139506707 | C | A | 1 | a0001c0005t0054 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4956G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4956 | chr4 | 139506707 | |||||
chr4:139506810 | G | C | 1 | a0001c0001t0052 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4853C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4853 | chr4 | 139506810 | |||||
chr4:139506827 | A | G | 1 | a0001c0001t0024 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4836T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4836 | chr4 | 139506827 | |||||
chr4:139506884 | G | A | 1 | a0001c0001t0041 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4779C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4779 | chr4 | 139506884 | |||||
chr4:139506890 | C | T | 1 | a0001c0001t0039 | 1 | NA20805.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4773G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4773 | chr4 | 139506890 | |||||
chr4:139507011 | C | T | 1 | a0001c0001t0019 | 2 | HG00323.hp2 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4652G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4652 | chr4 | 139507011 | |||||
chr4:139507014 | G | A | 1 | a0001c0001t0024 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4649C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4649 | chr4 | 139507014 | |||||
chr4:139507108 | G | A | 1 | a0001c0001t0042 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4555C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4555 | chr4 | 139507108 | |||||
chr4:139507145 | C | T | 2 | a0001c0001t0008a0001c0001t0022 | 4 | HG02040.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4518G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4518 | chr4 | 139507145 | |||||
chr4:139507209 | A | T | 1 | a0001c0001t0028 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4454T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4454 | chr4 | 139507209 | |||||
chr4:139507377 | G | A | 2 | a0001c0001t0052a0001c0001t0055 | 2 | HG03195.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4286C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 4286 | chr4 | 139507377 | |||||
chr4:139507676 | C | T | 1 | a0001c0001t0038 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3987G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3987 | chr4 | 139507676 | |||||
chr4:139508162 | T | C | 1 | a0001c0001t0043 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3501A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3501 | chr4 | 139508162 | |||||
chr4:139508258 | T | G | 2 | a0001c0001t0004a0001c0001t0028 | 8 | HG02055.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3405A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3405 | chr4 | 139508258 | |||||
chr4:139508364 | C | T | 2 | a0001c0001t0018a0001c0006t0018 | 2 | HG00423.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3299G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3299 | chr4 | 139508364 | |||||
chr4:139508401 | C | T | 26 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(23): Show | 77 | HG00099.hp1 HG00438.hp1 HG00642.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3262G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3262 | chr4 | 139508401 | |||||
chr4:139508410 | C | T | 2 | a0001c0001t0007a0001c0001t0015 | 6 | HG02809.hp2 HG02895.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3253G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3253 | chr4 | 139508410 | |||||
chr4:139508445 | T | C | 1 | a0001c0001t0013 | 3 | HG02145.hp2 HG02809.hp1 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3218A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3218 | chr4 | 139508445 | |||||
chr4:139508446 | G | A | 1 | a0001c0001t0029 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3217C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3217 | chr4 | 139508446 | |||||
chr4:139508615 | C | T | 1 | a0001c0001t0037 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3048G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3048 | chr4 | 139508615 | |||||
chr4:139508625 | C | T | 1 | a0001c0001t0047 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3038G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3038 | chr4 | 139508625 | |||||
chr4:139508648 | G | A | 1 | a0001c0001t0029 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3015C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 3015 | chr4 | 139508648 | |||||
chr4:139508696 | G | A | 1 | a0001c0001t0044 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2967C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2967 | chr4 | 139508696 | |||||
chr4:139508716 | G | A | 2 | a0001c0002t0010a0001c0006t0045 | 4 | HG00438.hp1 HG02148.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2947C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2947 | chr4 | 139508716 | |||||
chr4:139508775 | T | G | 1 | a0001c0001t0007 | 4 | HG02895.hp2 HG03130.hp1 NA19030.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2888A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2888 | chr4 | 139508775 | |||||
chr4:139508870 | C | G | 2 | a0001c0001t0049a0001c0002t0010 | 4 | HG01496.hp1 HG02148.hp2 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2793G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2793 | chr4 | 139508870 | |||||
chr4:139508907 | C | T | 1 | a0001c0001t0036 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2756G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2756 | chr4 | 139508907 | |||||
chr4:139509054 | C | G | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | 79 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2609G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2609 | chr4 | 139509054 | |||||
chr4:139509074 | C | T | 1 | a0001c0001t0015 | 2 | HG02809.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2589G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2589 | chr4 | 139509074 | |||||
chr4:139509102 | G | A | 8 | a0001c0001t0012a0001c0001t0013a0001c0001t0026others(5): Show | 11 | HG01192.hp1 HG01884.hp2 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2561C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2561 | chr4 | 139509102 | |||||
chr4:139509131 | G | A | 1 | a0001c0001t0009 | 3 | HG02280.hp1 HG03195.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2532C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2532 | chr4 | 139509131 | |||||
chr4:139509150 | G | C | 1 | a0001c0001t0047 | 1 | NA18997.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2513C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2513 | chr4 | 139509150 | |||||
chr4:139509157 | A | G | 6 | a0001c0001t0006a0001c0001t0034a0001c0001t0049others(3): Show | 11 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2506T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2506 | chr4 | 139509157 | |||||
chr4:139509278 | C | T | 1 | a0001c0004t0033 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2385G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2385 | chr4 | 139509278 | |||||
chr4:139509344 | A | G | 1 | a0001c0001t0016 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2319T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2319 | chr4 | 139509344 | |||||
chr4:139509422 | C | T | 1 | a0001c0005t0054 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2241G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2241 | chr4 | 139509422 | |||||
chr4:139509427 | G | T | 61 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*2236C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2236 | chr4 | 139509427 | |||||
chr4:139509471 | A | C | 38 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(35): Show | 238 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(235): Show |
3_prime_UTR_variant | MODIFIER | c.*2192T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2192 | chr4 | 139509471 | |||||
chr4:139509471 | A | G | 1 | a0001c0001t0032 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2192T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2192 | chr4 | 139509471 | |||||
chr4:139509537 | C | T | 1 | a0001c0001t0031 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2126G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2126 | chr4 | 139509537 | |||||
chr4:139509592 | T | C | 62 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(59): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
3_prime_UTR_variant | MODIFIER | c.*2071A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 2071 | chr4 | 139509592 | |||||
chr4:139510185 | C | T | 3 | a0001c0001t0020a0001c0001t0051a0001c0005t0058 | 4 | HG02965.hp2 HG03516.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1478G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1478 | chr4 | 139510185 | |||||
chr4:139510238 | ACAGATCA others(9): Show |
A | 37 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(34): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*1409_*1424delCTGT others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1409 | chr4 | 139510238 | |||||
chr4:139510350 | G | A | 1 | a0001c0001t0048 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1313C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1313 | chr4 | 139510350 | |||||
chr4:139510356 | A | T | 1 | a0001c0001t0024 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1307 | chr4 | 139510356 | |||||
chr4:139510635 | T | A | 2 | a0001c0001t0049a0001c0005t0058 | 2 | HG01496.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1028A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 1028 | chr4 | 139510635 | |||||
chr4:139510757 | T | G | 1 | a0001c0001t0050 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*906A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 906 | chr4 | 139510757 | |||||
chr4:139510777 | T | C | 16 | a0001c0001t0006a0001c0001t0011a0001c0001t0012others(13): Show | 27 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*886A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 886 | chr4 | 139510777 | |||||
chr4:139510798 | C | T | 1 | a0001c0001t0023 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*865G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 865 | chr4 | 139510798 | |||||
chr4:139511440 | A | T | 1 | a0001c0001t0022 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*223T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 223 | chr4 | 139511440 | |||||
chr4:139511451 | C | T | 1 | a0001c0001t0021 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*212G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 212 | chr4 | 139511451 | |||||
chr4:139511563 | G | A | 1 | a0001c0001t0059 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 8/8 | 100 | chr4 | 139511563 | |||||
chr4:139556145 | G | A | 1 | a0001c0001t0060 | 1 | NA18986.hp2 | 5_prime_UTR_variant | MODIFIER | c.-8C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/8 | 8 | chr4 | 139556145 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139512042 | C | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0103others(6): Show | 12 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.921-199G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512042 | ||||||
chr4:139512303 | G | T | 2 | a0001c0001t0001g0204a0001c0001t0040g0288 | 2 | HG02257.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.921-460C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512303 | ||||||
chr4:139512311 | A | G | 4 | a0001c0001t0001g0183a0001c0001t0009g0125a0001c0001t0009g0146others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-468T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512311 | ||||||
chr4:139512434 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.921-591A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512434 | ||||||
chr4:139512483 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.921-640C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512483 | ||||||
chr4:139512595 | G | A | 4 | a0001c0001t0001g0183a0001c0001t0009g0125a0001c0001t0009g0146others(1): Show | 4 | HG02109.hp2 HG02280.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.921-752C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512595 | ||||||
chr4:139512670 | A | G | 2 | a0001c0001t0001g0061a0001c0001t0060g0291 | 2 | NA18948.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.921-827T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512670 | ||||||
chr4:139512752 | C | CT | 13 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0002g0051others(10): Show | 14 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.921-910dupA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512752 | ||||||
chr4:139512752 | CT | C | 15 | a0001c0001t0006g0005a0001c0001t0006g0030a0001c0001t0011g0145others(12): Show | 17 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.921-910delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512752 | ||||||
chr4:139512752 | CTT | C | 27 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0038others(24): Show | 29 | HG01361.hp1 HG02027.hp1 HG02027.hp2 others(26): Show |
intron_variant | MODIFIER | c.921-911_921-910del others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512752 | ||||||
chr4:139512752 | CTTT | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(203): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.921-912_921-910del others(3): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512752 | ||||||
chr4:139512906 | T | C | 271 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(268): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.921-1063A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512906 | ||||||
chr4:139512945 | G | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0198 | 2 | HG02630.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.921-1102C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139512945 | ||||||
chr4:139513211 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.921-1368C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513211 | ||||||
chr4:139513272 | T | G | 1 | a0001c0001t0001g0040 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.921-1429A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513272 | ||||||
chr4:139513335 | G | A | 1 | a0001c0001t0029g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.921-1492C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513335 | ||||||
chr4:139513419 | C | CA | 19 | a0001c0001t0001g0040a0001c0001t0001g0138a0001c0001t0002g0013others(16): Show | 20 | HG00099.hp1 HG00408.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.921-1577dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513419 | ||||||
chr4:139513453 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.921-1610A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513453 | ||||||
chr4:139513586 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.921-1743A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513586 | ||||||
chr4:139513593 | C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0219 | 3 | HG01099.hp2 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.921-1750G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513593 | ||||||
chr4:139513730 | C | T | 1 | a0001c0001t0051g0144 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.921-1887G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513730 | ||||||
chr4:139513878 | T | G | 1 | a0001c0001t0036g0109 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.921-2035A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513878 | ||||||
chr4:139513890 | A | G | 8 | a0001c0001t0006g0005a0001c0001t0006g0030a0001c0001t0049g0236others(5): Show | 9 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.921-2047T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513890 | ||||||
chr4:139513922 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.921-2079G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513922 | ||||||
chr4:139513977 | T | C | 1 | a0001c0005t0058g0282 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.921-2134A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139513977 | ||||||
chr4:139514052 | G | A | 1 | a0001c0001t0029g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.921-2209C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514052 | ||||||
chr4:139514135 | T | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.921-2292A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514135 | ||||||
chr4:139514163 | T | C | 56 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0002g0051others(53): Show | 60 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.921-2320A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514163 | ||||||
chr4:139514282 | GA | G | 79 | a0001c0001t0001g0036a0001c0001t0001g0059a0001c0001t0001g0072others(76): Show | 85 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.921-2440delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514282 | ||||||
chr4:139514373 | C | A | 1 | a0001c0001t0015g0212 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.921-2530G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514373 | ||||||
chr4:139514385 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.921-2542G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514385 | ||||||
chr4:139514403 | G | T | 18 | a0001c0001t0011g0145a0001c0001t0011g0188a0001c0001t0011g0189others(15): Show | 19 | HG01192.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.921-2560C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514403 | ||||||
chr4:139514468 | CAG | C | 66 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0002g0051others(63): Show | 72 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.921-2627_921-2626d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514468 | ||||||
chr4:139514478 | A | G | 1 | a0001c0001t0029g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.921-2635T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514478 | ||||||
chr4:139514482 | G | A | 1 | a0001c0001t0049g0236 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.921-2639C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514482 | ||||||
chr4:139514581 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.921-2738G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514581 | ||||||
chr4:139514719 | C | T | 1 | a0001c0001t0030g0245 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.921-2876G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139514719 | ||||||
chr4:139515167 | CAA | C | 30 | a0001c0001t0001g0009a0001c0001t0001g0119a0001c0001t0001g0131others(27): Show | 33 | HG01074.hp1 HG01175.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.920+2716_920+2717d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515167 | ||||||
chr4:139515167 | CAAA | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0023others(80): Show | 88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.920+2715_920+2717d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515167 | ||||||
chr4:139515167 | CAAAA | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(165): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.920+2714_920+2717d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515167 | ||||||
chr4:139515167 | CAAAAA | C | 7 | a0001c0001t0001g0035a0001c0001t0001g0073a0001c0001t0001g0219others(4): Show | 7 | HG00408.hp2 HG01099.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.920+2713_920+2717d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515167 | ||||||
chr4:139515492 | G | A | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(211): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.920+2393C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515492 | ||||||
chr4:139515637 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.920+2248T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515637 | ||||||
chr4:139515841 | T | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0271 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.920+2044A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515841 | ||||||
chr4:139515904 | C | G | 3 | a0001c0001t0001g0280a0001c0001t0031g0227a0001c0001t0053g0284 | 3 | HG01192.hp1 HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.920+1981G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515904 | ||||||
chr4:139515931 | T | G | 3 | a0001c0001t0011g0145a0001c0001t0011g0188a0001c0001t0011g0189 | 3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.920+1954A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515931 | ||||||
chr4:139515947 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.920+1938T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139515947 | ||||||
chr4:139516236 | C | T | 4 | a0001c0001t0001g0147a0002c0003t0001g0047a0002c0003t0001g0121others(1): Show | 4 | HG00099.hp2 HG00140.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.920+1649G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516236 | ||||||
chr4:139516290 | AC | A | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.920+1594delG | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516290 | ||||||
chr4:139516326 | C | G | 8 | a0001c0001t0006g0005a0001c0001t0006g0030a0001c0001t0049g0236others(5): Show | 9 | HG00642.hp2 HG01074.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.920+1559G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516326 | ||||||
chr4:139516332 | G | A | 16 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0002g0051others(13): Show | 17 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.920+1553C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516332 | ||||||
chr4:139516465 | CA | C | 10 | a0001c0001t0001g0026a0001c0001t0001g0137a0001c0001t0001g0138others(7): Show | 10 | HG01109.hp1 HG01192.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.920+1419delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516465 | ||||||
chr4:139516465 | CAA | C | 156 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0015others(153): Show | 166 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.920+1418_920+1419d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516465 | ||||||
chr4:139516465 | CAAA | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(103): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.920+1417_920+1419d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516465 | ||||||
chr4:139516481 | A | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0115 | 3 | HG01496.hp2 HG03239.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.920+1404T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516481 | ||||||
chr4:139516672 | T | A | 9 | a0001c0001t0007g0279a0001c0001t0013g0006a0001c0001t0013g0057others(6): Show | 10 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.920+1213A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516672 | ||||||
chr4:139516673 | A | T | 18 | a0001c0001t0001g0028a0001c0001t0001g0132a0001c0001t0001g0280others(15): Show | 20 | HG01175.hp2 HG01192.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.920+1212T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516673 | ||||||
chr4:139516674 | A | T | 1 | a0001c0001t0011g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.920+1211T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516674 | ||||||
chr4:139516879 | C | T | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(209): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.920+1006G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516879 | ||||||
chr4:139516936 | G | C | 1 | a0001c0001t0011g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.920+949C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516936 | ||||||
chr4:139516961 | T | G | 3 | a0001c0001t0001g0154a0001c0001t0001g0223a0001c0001t0001g0276 | 3 | HG02080.hp1 NA18952.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.920+924A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139516961 | ||||||
chr4:139517055 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.920+830T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517055 | ||||||
chr4:139517094 | G | C | 1 | a0001c0001t0027g0049 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.920+791C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517094 | ||||||
chr4:139517124 | G | C | 1 | a0001c0001t0049g0236 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.920+761C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517124 | ||||||
chr4:139517193 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.920+692C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517193 | ||||||
chr4:139517232 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.920+653A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517232 | ||||||
chr4:139517475 | CA | C | 35 | a0001c0001t0001g0280a0001c0001t0002g0013a0001c0001t0002g0044others(32): Show | 38 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.920+409delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | ||||||
chr4:139517475 | CAA | C | 16 | a0001c0001t0007g0279a0001c0001t0012g0228a0001c0001t0012g0230others(13): Show | 17 | HG02258.hp1 HG02486.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.920+408_920+409del others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | ||||||
chr4:139517475 | CAAA | C | 8 | a0001c0001t0003g0004a0001c0001t0003g0107a0001c0001t0003g0186others(5): Show | 10 | HG01884.hp1 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.920+407_920+409del others(3): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | ||||||
chr4:139517475 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0142 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.920+396_920+409del others(14): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | ||||||
chr4:139517475 | CAAAAAAA others(8): Show |
C | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.920+395_920+409del others(15): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | ||||||
chr4:139517475 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.920+394_920+409del others(16): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517475 | ||||||
chr4:139517571 | T | G | 1 | a0001c0001t0011g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.920+314A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517571 | ||||||
chr4:139517586 | C | T | 13 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0002g0051others(10): Show | 14 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.920+299G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517586 | ||||||
chr4:139517587 | G | A | 1 | a0001c0001t0017g0033 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.920+298C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517587 | ||||||
chr4:139517612 | G | A | 16 | a0001c0001t0007g0279a0001c0001t0012g0228a0001c0001t0012g0230others(13): Show | 17 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.920+273C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517612 | ||||||
chr4:139517722 | G | A | 3 | a0001c0001t0011g0145a0001c0001t0011g0188a0001c0001t0011g0189 | 3 | HG02559.hp1 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.920+163C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517722 | ||||||
chr4:139517753 | C | T | 14 | a0001c0001t0007g0279a0001c0001t0012g0228a0001c0001t0012g0230others(11): Show | 15 | HG02145.hp2 HG02258.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.920+132G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517753 | ||||||
chr4:139517858 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.920+27C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 7/7 | chr4 | 139517858 | ||||||
chr4:139518162 | C | T | 3 | a0001c0001t0001g0138a0001c0001t0001g0191a0001c0001t0050g0206 | 3 | HG01978.hp1 HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.763-120G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518162 | ||||||
chr4:139518177 | G | C | 2 | a0001c0001t0001g0069a0001c0001t0001g0271 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.763-135C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518177 | ||||||
chr4:139518190 | G | A | 4 | a0001c0001t0012g0228a0001c0001t0012g0230a0001c0001t0057g0229others(1): Show | 4 | HG02258.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.763-148C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518190 | ||||||
chr4:139518232 | G | A | 3 | a0001c0001t0001g0248a0001c0002t0001g0209a0001c0002t0001g0210 | 3 | NA18970.hp1 NA18998.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.763-190C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518232 | ||||||
chr4:139518326 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.763-284T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518326 | ||||||
chr4:139518357 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.763-315C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139518357 | ||||||
chr4:139519064 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.763-1022A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139519064 | ||||||
chr4:139519338 | T | C | 3 | a0001c0001t0012g0228a0001c0001t0057g0229a0001c0004t0012g0251 | 3 | HG02717.hp1 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.762+939A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139519338 | ||||||
chr4:139520104 | T | TA | 13 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(10): Show | 14 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.762+172dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 6/7 | chr4 | 139520104 | ||||||
chr4:139520423 | C | T | 2 | a0001c0001t0001g0045a0001c0001t0001g0203 | 2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.645-29G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520423 | ||||||
chr4:139520540 | A | T | 1 | a0001c0001t0015g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.645-146T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520540 | ||||||
chr4:139520712 | T | C | 16 | a0001c0001t0001g0286a0001c0001t0004g0200a0001c0001t0004g0201others(13): Show | 17 | HG01361.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.645-318A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520712 | ||||||
chr4:139520718 | C | G | 3 | a0001c0001t0001g0286a0001c0001t0014g0056a0001c0001t0049g0236 | 3 | HG01496.hp1 HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.645-324G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520718 | ||||||
chr4:139520857 | T | C | 1 | a0001c0001t0006g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.645-463A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520857 | ||||||
chr4:139520991 | A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(232): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.645-597T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139520991 | ||||||
chr4:139521151 | C | T | 2 | a0001c0001t0009g0146a0001c0001t0053g0284 | 2 | HG01192.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.645-757G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521151 | ||||||
chr4:139521197 | G | A | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 44 | HG00423.hp1 HG00735.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.645-803C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521197 | ||||||
chr4:139521271 | C | CA | 14 | a0001c0001t0001g0043a0001c0001t0006g0005a0001c0001t0006g0030others(11): Show | 15 | HG00642.hp2 HG01074.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.645-878dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521271 | ||||||
chr4:139521290 | G | A | 6 | a0001c0001t0001g0280a0001c0001t0015g0212a0001c0001t0015g0242others(3): Show | 6 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-896C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521290 | ||||||
chr4:139521319 | G | T | 13 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(10): Show | 14 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.645-925C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521319 | ||||||
chr4:139521354 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.645-960G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521354 | ||||||
chr4:139521407 | C | T | 2 | a0001c0001t0001g0043a0001c0001t0035g0022 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.645-1013G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521407 | ||||||
chr4:139521426 | TA | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(286): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.645-1033delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521426 | ||||||
chr4:139521593 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.645-1199G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521593 | ||||||
chr4:139521910 | G | C | 1 | a0001c0001t0014g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.644+1444C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521910 | ||||||
chr4:139521921 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.644+1433G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139521921 | ||||||
chr4:139522190 | G | C | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.644+1164C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522190 | ||||||
chr4:139522362 | G | A | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 44 | HG00423.hp1 HG00735.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.644+992C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522362 | ||||||
chr4:139522411 | C | T | 8 | a0001c0001t0005g0008a0001c0001t0005g0062a0001c0001t0005g0063others(5): Show | 9 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.644+943G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522411 | ||||||
chr4:139522493 | T | C | 3 | a0001c0001t0001g0009a0001c0001t0043g0256a0001c0001t0048g0087 | 4 | HG01074.hp1 HG01192.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+861A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522493 | ||||||
chr4:139522662 | G | A | 1 | a0001c0002t0001g0210 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.644+692C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522662 | ||||||
chr4:139522662 | G | C | 1 | a0001c0001t0055g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.644+692C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522662 | ||||||
chr4:139522741 | C | CT | 11 | a0001c0001t0006g0005a0001c0001t0007g0279a0001c0001t0013g0006others(8): Show | 13 | HG01515.hp2 HG01517.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.644+612dupA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | ||||||
chr4:139522741 | C | CTT | 43 | a0001c0001t0001g0043a0001c0001t0001g0213a0001c0001t0001g0221others(40): Show | 44 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.644+611_644+612dup others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | ||||||
chr4:139522741 | C | CTTT | 9 | a0001c0001t0001g0019a0001c0001t0001g0074a0001c0001t0001g0126others(6): Show | 10 | HG01175.hp1 HG01361.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.644+610_644+612dup others(3): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | ||||||
chr4:139522741 | CT | C | 109 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(106): Show | 114 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.644+612delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | ||||||
chr4:139522741 | CTT | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(98): Show | 117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.644+611_644+612del others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | ||||||
chr4:139522741 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0015g0212a0001c0001t0028g0215 | 2 | HG02486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.644+601_644+612del others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522741 | ||||||
chr4:139522808 | C | T | 2 | a0001c0001t0001g0043a0001c0001t0035g0022 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.644+546G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522808 | ||||||
chr4:139522870 | C | T | 18 | a0001c0001t0001g0074a0001c0001t0001g0213a0001c0001t0001g0248others(15): Show | 19 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.644+484G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139522870 | ||||||
chr4:139523025 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.644+329T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 5/7 | chr4 | 139523025 | ||||||
chr4:139523604 | G | A | 1 | a0001c0001t0032g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.563-169C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139523604 | ||||||
chr4:139523729 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.563-294C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139523729 | ||||||
chr4:139523832 | A | G | 2 | a0001c0001t0001g0043a0001c0001t0035g0022 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.563-397T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139523832 | ||||||
chr4:139524256 | C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0126a0001c0001t0001g0204 | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-821G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524256 | ||||||
chr4:139524344 | G | T | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.563-909C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524344 | ||||||
chr4:139524553 | G | C | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.563-1118C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524553 | ||||||
chr4:139524687 | T | A | 2 | a0001c0001t0001g0156a0001c0001t0001g0170 | 2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.563-1252A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524687 | ||||||
chr4:139524816 | C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0263 | 2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.563-1381G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524816 | ||||||
chr4:139524851 | C | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0126a0001c0001t0001g0204 | 4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.563-1416G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524851 | ||||||
chr4:139524925 | T | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(101): Show | 120 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.563-1490A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139524925 | ||||||
chr4:139525146 | T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.563-1711A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525146 | ||||||
chr4:139525210 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.563-1775T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525210 | ||||||
chr4:139525239 | G | A | 18 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0126others(15): Show | 19 | HG01496.hp1 HG01891.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.563-1804C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525239 | ||||||
chr4:139525263 | G | T | 2 | a0001c0001t0003g0186a0001c0001t0003g0187 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.563-1828C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525263 | ||||||
chr4:139525337 | C | G | 2 | a0001c0001t0011g0188a0001c0001t0011g0189 | 2 | HG02559.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.563-1902G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525337 | ||||||
chr4:139525375 | C | T | 1 | a0001c0001t0047g0192 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.563-1940G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525375 | ||||||
chr4:139525428 | C | T | 2 | a0001c0002t0001g0211a0001c0002t0010g0208 | 2 | NA18960.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.563-1993G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525428 | ||||||
chr4:139525524 | T | TA | 11 | a0001c0001t0001g0221a0001c0001t0001g0243a0001c0001t0001g0244others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.563-2090dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525524 | ||||||
chr4:139525574 | C | A | 1 | a0001c0002t0006g0136 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.563-2139G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525574 | ||||||
chr4:139525613 | G | GAATTA | 3 | a0001c0004t0001g0252a0001c0004t0012g0251a0001c0004t0033g0071 | 3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.563-2183_563-2179d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525613 | ||||||
chr4:139525732 | T | C | 4 | a0001c0001t0008g0025a0001c0001t0008g0268a0001c0001t0008g0269others(1): Show | 4 | HG02040.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.563-2297A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525732 | ||||||
chr4:139525738 | G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.563-2303C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525738 | ||||||
chr4:139525763 | C | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0018others(9): Show | 16 | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.563-2328G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525763 | ||||||
chr4:139525930 | A | G | 22 | a0001c0001t0001g0074a0001c0001t0001g0213a0001c0001t0001g0248others(19): Show | 24 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.563-2495T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525930 | ||||||
chr4:139525951 | A | C | 104 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(101): Show | 108 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.563-2516T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525951 | ||||||
chr4:139525983 | C | T | 55 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(52): Show | 56 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.563-2548G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139525983 | ||||||
chr4:139526044 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.563-2609C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526044 | ||||||
chr4:139526046 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.563-2611A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526046 | ||||||
chr4:139526046 | T | TTTTGTTT others(1): Show |
3 | a0001c0001t0020g0238a0001c0005t0054g0283a0001c0005t0058g0282 | 3 | HG02965.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.563-2619_563-2612d others(10): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526046 | ||||||
chr4:139526046 | TTTTG | T | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.563-2615_563-2612d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526046 | ||||||
chr4:139526200 | T | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.563-2765A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526200 | ||||||
chr4:139526274 | A | AT | 20 | a0001c0001t0001g0024a0001c0001t0001g0043a0001c0001t0001g0234others(17): Show | 21 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.562+2756dupA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526274 | ||||||
chr4:139526274 | AT | A | 8 | a0001c0001t0001g0119a0001c0001t0001g0129a0001c0001t0001g0182others(5): Show | 8 | HG00323.hp1 HG00323.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.562+2756delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526274 | ||||||
chr4:139526291 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.562+2740T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526291 | ||||||
chr4:139526407 | T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(110): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.562+2624A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526407 | ||||||
chr4:139526436 | A | AT | 43 | a0001c0001t0001g0015a0001c0001t0001g0046a0001c0001t0001g0060others(40): Show | 44 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.562+2594dupA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526436 | ||||||
chr4:139526436 | A | ATTT | 14 | a0001c0001t0001g0041a0001c0001t0001g0127a0001c0001t0001g0153others(11): Show | 14 | HG01934.hp2 HG02056.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.562+2592_562+2594d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526436 | ||||||
chr4:139526436 | AT | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(185): Show | 207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.562+2594delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526436 | ||||||
chr4:139526946 | A | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.562+2085T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139526946 | ||||||
chr4:139527130 | A | G | 1 | a0001c0001t0032g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.562+1901T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527130 | ||||||
chr4:139527435 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.562+1596C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527435 | ||||||
chr4:139527465 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.562+1566C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527465 | ||||||
chr4:139527477 | G | C | 39 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0026others(36): Show | 41 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.562+1554C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527477 | ||||||
chr4:139527619 | A | G | 14 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(11): Show | 15 | HG01361.hp1 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.562+1412T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139527619 | ||||||
chr4:139528071 | A | G | 3 | a0001c0001t0001g0280a0001c0001t0031g0227a0001c0001t0053g0284 | 3 | HG01192.hp1 HG02055.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.562+960T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528071 | ||||||
chr4:139528251 | C | T | 1 | a0001c0001t0014g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562+780G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528251 | ||||||
chr4:139528266 | T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(112): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.562+765A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528266 | ||||||
chr4:139528310 | G | A | 1 | a0001c0001t0049g0236 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.562+721C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528310 | ||||||
chr4:139528495 | T | C | 67 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0040others(64): Show | 70 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.562+536A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528495 | ||||||
chr4:139528670 | T | C | 65 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0021others(62): Show | 69 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.562+361A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528670 | ||||||
chr4:139528844 | C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0263 | 2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.562+187G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528844 | ||||||
chr4:139528923 | G | A | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.562+108C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 4/7 | chr4 | 139528923 | ||||||
chr4:139529270 | G | A | 4 | a0001c0001t0001g0074a0001c0001t0001g0213a0001c0001t0001g0248others(1): Show | 4 | HG02074.hp2 NA18948.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-50C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529270 | ||||||
chr4:139529301 | G | C | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(257): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.373-81C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529301 | ||||||
chr4:139529350 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.373-130G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529350 | ||||||
chr4:139529492 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.373-272G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529492 | ||||||
chr4:139529627 | C | T | 8 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211others(5): Show | 8 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.373-407G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529627 | ||||||
chr4:139529730 | C | A | 7 | a0001c0001t0001g0043a0001c0001t0001g0286a0001c0001t0014g0056others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-510G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529730 | ||||||
chr4:139529892 | T | A | 1 | a0001c0001t0002g0054 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.373-672A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529892 | ||||||
chr4:139529919 | C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0102 | 3 | NA18974.hp2 NA18978.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.373-699G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529919 | ||||||
chr4:139529979 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.373-759G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139529979 | ||||||
chr4:139530082 | G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.373-862C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530082 | ||||||
chr4:139530165 | T | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0234a0001c0001t0039g0257others(8): Show | 11 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.373-945A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530165 | ||||||
chr4:139530223 | G | A | 40 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0021others(37): Show | 42 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.373-1003C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530223 | ||||||
chr4:139530235 | A | G | 7 | a0001c0001t0001g0043a0001c0001t0001g0286a0001c0001t0014g0056others(4): Show | 7 | HG01891.hp2 HG02717.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-1015T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530235 | ||||||
chr4:139530356 | CTT | C | 49 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0026others(46): Show | 51 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.373-1138_373-1137d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | ||||||
chr4:139530356 | CTTT | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.373-1139_373-1137d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | ||||||
chr4:139530356 | CTTTT | C | 66 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0040others(63): Show | 69 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.373-1140_373-1137d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | ||||||
chr4:139530356 | CTTTTT | C | 17 | a0001c0001t0001g0019a0001c0001t0001g0126a0001c0001t0001g0148others(14): Show | 18 | HG00438.hp1 HG01192.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.373-1141_373-1137d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | ||||||
chr4:139530356 | CTTTTTT | C | 21 | a0001c0001t0001g0043a0001c0001t0001g0074a0001c0001t0001g0213others(18): Show | 23 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.373-1142_373-1137d others(8): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530356 | ||||||
chr4:139530359 | T | C | 1 | a0001c0001t0052g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.373-1139A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530359 | ||||||
chr4:139530395 | TG | T | 41 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0021others(38): Show | 43 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.373-1176delC | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530395 | ||||||
chr4:139530398 | A | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 174 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.373-1178T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530398 | ||||||
chr4:139530690 | C | T | 1 | a0001c0001t0032g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.373-1470G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530690 | ||||||
chr4:139530691 | A | C | 1 | a0001c0001t0002g0117 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.373-1471T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530691 | ||||||
chr4:139530933 | C | T | 130 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(127): Show | 135 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.373-1713G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139530933 | ||||||
chr4:139531106 | A | C | 3 | a0001c0001t0001g0023a0001c0001t0001g0100a0001c0001t0042g0099 | 3 | HG00597.hp1 HG02083.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.373-1886T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531106 | ||||||
chr4:139531251 | G | A | 12 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0126others(9): Show | 14 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+1914C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531251 | ||||||
chr4:139531400 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.372+1765G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531400 | ||||||
chr4:139531487 | C | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0219others(3): Show | 7 | HG00140.hp2 HG00438.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+1678G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531487 | ||||||
chr4:139531613 | T | C | 72 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0040others(69): Show | 74 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.372+1552A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531613 | ||||||
chr4:139531669 | T | G | 56 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(53): Show | 57 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.372+1496A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531669 | ||||||
chr4:139531752 | C | T | 1 | a0001c0002t0010g0208 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.372+1413G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531752 | ||||||
chr4:139531808 | C | T | 6 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0001t0001g0243others(3): Show | 6 | HG02004.hp1 HG02486.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+1357G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531808 | ||||||
chr4:139531842 | G | A | 3 | a0001c0001t0001g0218a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG00408.hp2 HG00597.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.372+1323C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531842 | ||||||
chr4:139531950 | C | T | 2 | a0001c0001t0001g0043a0001c0001t0035g0022 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.372+1215G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531950 | ||||||
chr4:139531951 | G | A | 1 | a0001c0001t0003g0070 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.372+1214C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531951 | ||||||
chr4:139531957 | A | G | 114 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(111): Show | 120 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.372+1208T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139531957 | ||||||
chr4:139532008 | C | T | 1 | a0001c0001t0038g0222 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.372+1157G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532008 | ||||||
chr4:139532043 | G | A | 1 | a0001c0001t0053g0284 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.372+1122C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532043 | ||||||
chr4:139532079 | G | A | 6 | a0001c0001t0001g0120a0001c0001t0001g0181a0001c0001t0002g0122others(3): Show | 6 | HG00280.hp1 HG02257.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+1086C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532079 | ||||||
chr4:139532215 | G | T | 27 | a0001c0001t0001g0074a0001c0001t0001g0179a0001c0001t0001g0213others(24): Show | 30 | HG00099.hp1 HG00642.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.372+950C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532215 | ||||||
chr4:139532329 | C | T | 15 | a0001c0001t0001g0021a0001c0001t0001g0198a0001c0001t0001g0221others(12): Show | 16 | HG01361.hp1 HG02004.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.372+836G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532329 | ||||||
chr4:139532336 | G | A | 103 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(100): Show | 109 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.372+829C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532336 | ||||||
chr4:139532378 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.372+787C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532378 | ||||||
chr4:139532394 | G | T | 10 | a0001c0001t0002g0013a0001c0001t0002g0044a0001c0001t0002g0051others(7): Show | 12 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.372+771C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532394 | ||||||
chr4:139532496 | T | A | 112 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0021others(109): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.372+669A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532496 | ||||||
chr4:139532574 | A | G | 1 | a0001c0001t0052g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.372+591T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532574 | ||||||
chr4:139532660 | TC | T | 14 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0001t0001g0243others(11): Show | 15 | HG01361.hp1 HG02004.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.372+504delG | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532660 | ||||||
chr4:139532764 | T | C | 6 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.372+401A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532764 | ||||||
chr4:139532777 | T | C | 1 | a0001c0001t0056g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.372+388A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532777 | ||||||
chr4:139532787 | G | A | 2 | a0001c0001t0001g0043a0001c0001t0035g0022 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.372+378C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532787 | ||||||
chr4:139532910 | A | C | 15 | a0001c0001t0001g0021a0001c0001t0001g0198a0001c0001t0001g0221others(12): Show | 16 | HG01361.hp1 HG02004.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.372+255T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139532910 | ||||||
chr4:139533033 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.372+132T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139533033 | ||||||
chr4:139533142 | G | C | 1 | a0001c0001t0001g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.372+23C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 3/7 | chr4 | 139533142 | ||||||
chr4:139533557 | C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.171-191G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533557 | ||||||
chr4:139533564 | T | G | 8 | a0001c0001t0005g0008a0001c0001t0005g0062a0001c0001t0005g0063others(5): Show | 9 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.171-198A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533564 | ||||||
chr4:139533770 | G | C | 1 | a0001c0001t0005g0062 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.171-404C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533770 | ||||||
chr4:139533892 | G | C | 10 | a0001c0001t0001g0039a0001c0001t0001g0139a0001c0001t0001g0140others(7): Show | 10 | HG00423.hp1 HG01257.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.171-526C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533892 | ||||||
chr4:139533908 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.171-542T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533908 | ||||||
chr4:139533965 | C | CTATG | 12 | a0001c0001t0001g0207a0001c0001t0002g0013a0001c0001t0002g0044others(9): Show | 14 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.171-603_171-600dup others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533965 | ||||||
chr4:139533965 | C | G | 7 | a0001c0001t0004g0185a0001c0001t0020g0238a0001c0001t0031g0227others(4): Show | 7 | HG01192.hp1 HG02055.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-599G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533965 | ||||||
chr4:139533965 | CTATG | C | 7 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0001t0001g0243others(4): Show | 7 | HG02486.hp2 HG02630.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-603_171-600del others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533965 | ||||||
chr4:139533982 | T | G | 6 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-616A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533982 | ||||||
chr4:139533986 | T | C | 65 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(62): Show | 66 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.171-620A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533986 | ||||||
chr4:139533993 | A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.171-627T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139533993 | ||||||
chr4:139534100 | C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(188): Show | 211 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.171-734G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534100 | ||||||
chr4:139534199 | A | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0126others(5): Show | 9 | HG02145.hp1 HG02451.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.171-833T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534199 | ||||||
chr4:139534320 | G | C | 1 | a0001c0001t0052g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.171-954C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534320 | ||||||
chr4:139534374 | A | C | 146 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(143): Show | 153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.171-1008T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534374 | ||||||
chr4:139534459 | C | T | 5 | a0001c0001t0001g0198a0001c0001t0001g0221a0001c0001t0001g0243others(2): Show | 5 | HG02486.hp2 HG02630.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.171-1093G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534459 | ||||||
chr4:139534498 | C | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0290a0001c0001t0014g0056 | 3 | HG01891.hp2 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.171-1132G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534498 | ||||||
chr4:139534609 | C | T | 8 | a0001c0001t0005g0008a0001c0001t0005g0062a0001c0001t0005g0063others(5): Show | 9 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.171-1243G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534609 | ||||||
chr4:139534712 | G | A | 3 | a0001c0004t0001g0252a0001c0004t0012g0251a0001c0004t0033g0071 | 3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.171-1346C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534712 | ||||||
chr4:139534789 | C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG01934.hp1 HG01943.hp1 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-1423G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534789 | ||||||
chr4:139534797 | G | A | 1 | a0001c0001t0014g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.171-1431C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534797 | ||||||
chr4:139534876 | T | C | 2 | a0001c0001t0001g0267a0001c0001t0001g0272 | 2 | HG00735.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.171-1510A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534876 | ||||||
chr4:139534952 | A | C | 9 | a0001c0001t0004g0185a0001c0001t0015g0212a0001c0001t0015g0242others(6): Show | 9 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-1586T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139534952 | ||||||
chr4:139535085 | T | C | 9 | a0001c0001t0004g0185a0001c0001t0015g0212a0001c0001t0015g0242others(6): Show | 9 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-1719A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535085 | ||||||
chr4:139535186 | ATG | A | 17 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0043others(14): Show | 19 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.171-1822_171-1821d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535186 | ||||||
chr4:139535407 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.171-2041A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535407 | ||||||
chr4:139535418 | T | C | 1 | a0001c0001t0034g0226 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.171-2052A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535418 | ||||||
chr4:139535534 | A | C | 9 | a0001c0001t0004g0185a0001c0001t0015g0212a0001c0001t0015g0242others(6): Show | 9 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-2168T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535534 | ||||||
chr4:139535538 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.171-2172C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535538 | ||||||
chr4:139535708 | T | C | 67 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(64): Show | 68 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.171-2342A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535708 | ||||||
chr4:139535887 | TA | T | 3 | a0001c0001t0008g0025a0001c0001t0008g0268a0001c0001t0008g0269 | 3 | HG02040.hp1 NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.171-2522delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535887 | ||||||
chr4:139535930 | A | G | 18 | a0001c0001t0001g0074a0001c0001t0001g0179a0001c0001t0001g0213others(15): Show | 21 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.171-2564T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139535930 | ||||||
chr4:139536114 | C | T | 4 | a0001c0001t0001g0179a0001c0001t0007g0279a0001c0001t0013g0006others(1): Show | 5 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-2748G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536114 | ||||||
chr4:139536147 | C | T | 1 | a0001c0001t0029g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.171-2781G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536147 | ||||||
chr4:139536253 | C | T | 2 | a0001c0001t0001g0043a0001c0001t0035g0022 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.171-2887G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536253 | ||||||
chr4:139536276 | G | T | 96 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 103 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.171-2910C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536276 | ||||||
chr4:139536517 | C | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(285): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.171-3151G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536517 | ||||||
chr4:139536709 | TA | T | 4 | a0001c0001t0001g0179a0001c0001t0007g0279a0001c0001t0013g0006others(1): Show | 5 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3344delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536709 | ||||||
chr4:139536725 | T | C | 1 | a0001c0006t0045g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.171-3359A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536725 | ||||||
chr4:139536743 | C | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3377G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536743 | ||||||
chr4:139536752 | C | T | 3 | a0001c0001t0001g0016a0001c0001t0011g0188a0001c0001t0011g0189 | 4 | HG02109.hp1 HG02559.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.171-3386G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536752 | ||||||
chr4:139536756 | C | T | 1 | a0001c0006t0045g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.171-3390G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536756 | ||||||
chr4:139536757 | C | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3391G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536757 | ||||||
chr4:139536761 | T | TG | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3396dupC | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536761 | ||||||
chr4:139536769 | G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3403C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536769 | ||||||
chr4:139536773 | C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3407G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536773 | ||||||
chr4:139536777 | A | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3411T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536777 | ||||||
chr4:139536783 | A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3417T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536783 | ||||||
chr4:139536785 | C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3419G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536785 | ||||||
chr4:139536791 | T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3425A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536791 | ||||||
chr4:139536797 | A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3431T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536797 | ||||||
chr4:139536801 | G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3435C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536801 | ||||||
chr4:139536803 | A | G | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3437T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536803 | ||||||
chr4:139536849 | A | G | 3 | a0001c0001t0015g0212a0001c0001t0015g0242a0001c0001t0028g0215 | 3 | HG02486.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.171-3483T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536849 | ||||||
chr4:139536957 | C | T | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.171-3591G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139536957 | ||||||
chr4:139537067 | C | T | 2 | a0001c0001t0003g0107a0001c0001t0003g0197 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.171-3701G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537067 | ||||||
chr4:139537108 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.171-3742G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537108 | ||||||
chr4:139537122 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.171-3756G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537122 | ||||||
chr4:139537137 | A | G | 155 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(152): Show | 163 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.171-3771T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537137 | ||||||
chr4:139537163 | C | T | 1 | a0001c0001t0011g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.171-3797G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537163 | ||||||
chr4:139537289 | T | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0218a0001c0001t0001g0224others(2): Show | 5 | HG00408.hp2 HG00597.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-3923A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537289 | ||||||
chr4:139537307 | G | A | 2 | a0001c0001t0001g0021a0001c0001t0047g0192 | 2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.171-3941C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537307 | ||||||
chr4:139537317 | T | C | 1 | a0001c0001t0001g0280 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.171-3951A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537317 | ||||||
chr4:139537484 | C | CA | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(111): Show | 129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.171-4119dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537484 | ||||||
chr4:139537485 | A | C | 1 | a0001c0001t0001g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.171-4119T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537485 | ||||||
chr4:139537518 | C | T | 41 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0026others(38): Show | 43 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.171-4152G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537518 | ||||||
chr4:139537826 | G | A | 3 | a0001c0001t0001g0286a0001c0001t0001g0290a0001c0001t0014g0056 | 3 | HG01891.hp2 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.171-4460C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537826 | ||||||
chr4:139537901 | C | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0085a0001c0001t0001g0093others(3): Show | 7 | HG00423.hp2 HG00621.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.171-4535G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139537901 | ||||||
chr4:139538017 | G | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.171-4651C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538017 | ||||||
chr4:139538105 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.171-4739A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538105 | ||||||
chr4:139538106 | T | C | 1 | a0001c0001t0035g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.171-4740A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538106 | ||||||
chr4:139538172 | G | T | 1 | a0001c0001t0021g0080 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.171-4806C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538172 | ||||||
chr4:139538203 | A | G | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(189): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.171-4837T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538203 | ||||||
chr4:139538484 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.171-5118G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538484 | ||||||
chr4:139538548 | C | G | 2 | a0001c0001t0002g0089a0001c0001t0002g0090 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.171-5182G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538548 | ||||||
chr4:139538548 | C | T | 1 | a0001c0001t0011g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.171-5182G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538548 | ||||||
chr4:139538568 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.171-5202T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538568 | ||||||
chr4:139538574 | C | T | 6 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-5208G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538574 | ||||||
chr4:139538630 | T | C | 6 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.171-5264A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538630 | ||||||
chr4:139538697 | T | TACATAAT others(329): Show |
1 | a0001c0001t0052g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.171-5332_171-5331i others(338): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538697 | ||||||
chr4:139538816 | G | A | 1 | a0001c0001t0021g0080 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.171-5450C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538816 | ||||||
chr4:139538996 | T | C | 3 | a0001c0001t0003g0107a0001c0001t0003g0197a0001c0001t0032g0086 | 3 | HG02886.hp1 HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.171-5630A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139538996 | ||||||
chr4:139539002 | T | G | 4 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0149others(1): Show | 4 | HG01257.hp1 HG01943.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-5636A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539002 | ||||||
chr4:139539149 | C | T | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(200): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.171-5783G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539149 | ||||||
chr4:139539164 | G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0126a0001c0001t0001g0203others(2): Show | 6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.171-5798C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539164 | ||||||
chr4:139539473 | C | T | 2 | a0001c0001t0016g0262a0001c0001t0016g0264 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.171-6107G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539473 | ||||||
chr4:139539502 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.171-6136A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539502 | ||||||
chr4:139539669 | C | T | 6 | a0001c0001t0001g0015a0001c0001t0001g0156a0001c0001t0001g0170others(3): Show | 7 | HG00558.hp2 HG02027.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.171-6303G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139539669 | ||||||
chr4:139540023 | C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0126a0001c0001t0001g0203others(2): Show | 6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.171-6657G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540023 | ||||||
chr4:139540118 | C | T | 9 | a0001c0001t0004g0185a0001c0001t0015g0212a0001c0001t0015g0242others(6): Show | 9 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-6752G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540118 | ||||||
chr4:139540387 | G | A | 2 | a0001c0001t0044g0048a0002c0003t0001g0047 | 2 | HG00099.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.170+6533C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540387 | ||||||
chr4:139540405 | G | T | 1 | a0001c0006t0045g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.170+6515C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540405 | ||||||
chr4:139540498 | C | T | 1 | a0001c0001t0032g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.170+6422G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540498 | ||||||
chr4:139540547 | G | C | 1 | a0001c0001t0036g0109 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.170+6373C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540547 | ||||||
chr4:139540563 | A | T | 19 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0043others(16): Show | 21 | HG01496.hp1 HG02055.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.170+6357T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540563 | ||||||
chr4:139540660 | G | A | 19 | a0001c0001t0001g0074a0001c0001t0001g0179a0001c0001t0001g0213others(16): Show | 22 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.170+6260C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540660 | ||||||
chr4:139540759 | T | C | 10 | a0001c0001t0001g0148a0001c0001t0004g0185a0001c0001t0015g0212others(7): Show | 10 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.170+6161A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540759 | ||||||
chr4:139540961 | A | G | 1 | a0001c0001t0011g0188 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.170+5959T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540961 | ||||||
chr4:139540976 | G | A | 2 | a0001c0001t0001g0021a0001c0001t0047g0192 | 2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.170+5944C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139540976 | ||||||
chr4:139541125 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.170+5795C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541125 | ||||||
chr4:139541247 | T | C | 178 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(175): Show | 188 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.170+5673A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541247 | ||||||
chr4:139541272 | G | C | 15 | a0001c0001t0001g0074a0001c0001t0001g0213a0001c0001t0001g0246others(12): Show | 17 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.170+5648C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541272 | ||||||
chr4:139541325 | A | G | 2 | a0001c0001t0016g0262a0001c0001t0016g0264 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.170+5595T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541325 | ||||||
chr4:139541369 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.170+5551T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541369 | ||||||
chr4:139541503 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170+5417C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541503 | ||||||
chr4:139541609 | G | A | 2 | a0001c0001t0001g0043a0001c0001t0035g0022 | 2 | HG02818.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.170+5311C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541609 | ||||||
chr4:139541625 | T | G | 179 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(176): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.170+5295A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541625 | ||||||
chr4:139541966 | C | T | 9 | a0001c0001t0004g0233a0001c0002t0001g0209a0001c0002t0001g0210others(6): Show | 9 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.170+4954G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541966 | ||||||
chr4:139541970 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170+4950C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139541970 | ||||||
chr4:139542012 | A | G | 9 | a0001c0001t0004g0233a0001c0002t0001g0209a0001c0002t0001g0210others(6): Show | 9 | HG00642.hp2 HG01074.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.170+4908T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542012 | ||||||
chr4:139542107 | G | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0110a0001c0001t0001g0112others(2): Show | 5 | HG02523.hp2 NA18955.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.170+4813C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542107 | ||||||
chr4:139542127 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170+4793A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542127 | ||||||
chr4:139542200 | A | G | 1 | a0001c0001t0006g0030 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.170+4720T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542200 | ||||||
chr4:139542411 | A | G | 6 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+4509T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542411 | ||||||
chr4:139542481 | TA | T | 6 | a0001c0001t0005g0008a0001c0001t0005g0062a0001c0001t0005g0063others(3): Show | 7 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+4438delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542481 | ||||||
chr4:139542503 | C | A | 1 | a0001c0001t0001g0250 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.170+4417G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542503 | ||||||
chr4:139542504 | C | A | 2 | a0001c0001t0001g0021a0001c0001t0047g0192 | 2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.170+4416G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542504 | ||||||
chr4:139542554 | C | G | 174 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(171): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.170+4366G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542554 | ||||||
chr4:139542810 | G | C | 1 | a0001c0001t0001g0045 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.170+4110C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542810 | ||||||
chr4:139542845 | C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0126a0001c0001t0001g0203others(2): Show | 6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.170+4075G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542845 | ||||||
chr4:139542862 | C | G | 1 | a0001c0001t0001g0259 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.170+4058G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542862 | ||||||
chr4:139542940 | T | C | 6 | a0001c0001t0004g0185a0001c0001t0031g0227a0001c0001t0053g0284others(3): Show | 6 | HG01192.hp1 HG02055.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+3980A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542940 | ||||||
chr4:139542962 | C | G | 2 | a0001c0001t0031g0227a0001c0001t0053g0284 | 2 | HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.170+3958G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139542962 | ||||||
chr4:139543111 | C | T | 53 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(50): Show | 54 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.170+3809G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543111 | ||||||
chr4:139543354 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.170+3566A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543354 | ||||||
chr4:139543539 | A | G | 42 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0026others(39): Show | 44 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.170+3381T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543539 | ||||||
chr4:139543608 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.170+3312A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543608 | ||||||
chr4:139543676 | G | T | 1 | a0001c0006t0045g0266 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.170+3244C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543676 | ||||||
chr4:139543719 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.170+3201T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543719 | ||||||
chr4:139543724 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.170+3196C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543724 | ||||||
chr4:139543727 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.170+3193G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543727 | ||||||
chr4:139543756 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.170+3164A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543756 | ||||||
chr4:139543768 | A | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0088 | 2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.170+3152T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543768 | ||||||
chr4:139543798 | C | CA | 24 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0113others(21): Show | 25 | HG01106.hp2 HG01261.hp2 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.170+3121dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | ||||||
chr4:139543798 | C | CAA | 7 | a0001c0001t0001g0078a0001c0001t0001g0148a0001c0001t0001g0286others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+3120_170+3121d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | ||||||
chr4:139543798 | C | CAAA | 9 | a0001c0001t0001g0021a0001c0001t0004g0233a0001c0001t0047g0192others(6): Show | 9 | HG02148.hp2 HG02622.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+3119_170+3121d others(5): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | ||||||
chr4:139543798 | C | CAAAAA | 38 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0026others(35): Show | 40 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.170+3117_170+3121d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | ||||||
chr4:139543798 | C | CAAAAAA | 63 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0040others(60): Show | 64 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.170+3116_170+3121d others(8): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | ||||||
chr4:139543798 | CA | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0092a0001c0001t0001g0126others(10): Show | 14 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.170+3121delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543798 | ||||||
chr4:139543824 | CGTGGTG | C | 6 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+3090_170+3095d others(8): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543824 | ||||||
chr4:139543857 | A | G | 1 | a0001c0001t0009g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.170+3063T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543857 | ||||||
chr4:139543924 | G | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0263 | 2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.170+2996C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543924 | ||||||
chr4:139543962 | T | TCAAA | 72 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0016others(69): Show | 77 | HG00423.hp1 HG00735.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.170+2954_170+2957d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543962 | ||||||
chr4:139543962 | T | TCAAACAA others(1): Show |
68 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0041others(65): Show | 71 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.170+2950_170+2957d others(10): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543962 | ||||||
chr4:139543962 | T | TCAAACAA others(5): Show |
8 | a0001c0001t0001g0131a0001c0001t0001g0165a0001c0001t0001g0166others(5): Show | 8 | HG00280.hp2 HG01255.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.170+2946_170+2957d others(14): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139543962 | ||||||
chr4:139544060 | G | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0213a0001c0001t0027g0049 | 3 | HG02074.hp2 NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.170+2860C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544060 | ||||||
chr4:139544163 | G | T | 18 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0219others(15): Show | 20 | HG00140.hp2 HG00438.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.170+2757C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544163 | ||||||
chr4:139544195 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.170+2725C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544195 | ||||||
chr4:139544200 | G | C | 6 | a0001c0002t0001g0209a0001c0002t0001g0210a0001c0002t0001g0211others(3): Show | 6 | HG02148.hp2 HG03098.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.170+2720C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544200 | ||||||
chr4:139544274 | C | T | 99 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(96): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.170+2646G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544274 | ||||||
chr4:139544290 | C | CTAAAA | 32 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0116others(29): Show | 35 | HG00099.hp1 HG01074.hp1 HG01169.hp2 others(32): Show |
intron_variant | MODIFIER | c.170+2625_170+2629d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | ||||||
chr4:139544290 | C | CTAAAATA others(3): Show |
14 | a0001c0001t0004g0185a0001c0001t0004g0200a0001c0001t0004g0201others(11): Show | 14 | HG01106.hp2 HG01192.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.170+2620_170+2629d others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | ||||||
chr4:139544290 | C | CTAAAATA others(8): Show |
7 | a0001c0001t0015g0212a0001c0001t0015g0242a0001c0001t0020g0020others(4): Show | 7 | HG01884.hp2 HG02486.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+2615_170+2629d others(17): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | ||||||
chr4:139544290 | C | CTAAAATA others(18): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0219a0001c0006t0018g0067others(1): Show | 5 | HG00438.hp1 HG01099.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+2605_170+2629d others(27): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | ||||||
chr4:139544290 | C | CTAAAATA others(23): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0220 | 2 | HG00140.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.170+2600_170+2629d others(32): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | ||||||
chr4:139544290 | CTAAAA | C | 95 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(92): Show | 98 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.170+2625_170+2629d others(7): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | ||||||
chr4:139544290 | CTAAAATA others(3): Show |
C | 9 | a0001c0001t0001g0120a0001c0001t0001g0181a0001c0001t0002g0122others(6): Show | 9 | HG00280.hp1 HG02257.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+2620_170+2629d others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | ||||||
chr4:139544290 | CTAAAATA others(8): Show |
C | 2 | a0001c0001t0001g0205a0001c0001t0001g0275 | 2 | HG02155.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.170+2615_170+2629d others(17): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544290 | ||||||
chr4:139544362 | GA | G | 6 | a0001c0001t0001g0179a0001c0001t0007g0177a0001c0001t0007g0178others(3): Show | 7 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+2557delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544362 | ||||||
chr4:139544455 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.170+2465C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544455 | ||||||
chr4:139544595 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.170+2325C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544595 | ||||||
chr4:139544797 | A | AGT | 12 | a0001c0001t0001g0066a0001c0001t0001g0088a0001c0001t0001g0152others(9): Show | 14 | HG00323.hp1 HG01109.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.170+2121_170+2122d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | A | AGTGT | 2 | a0001c0001t0001g0009a0001c0001t0048g0087 | 3 | HG01074.hp1 HG01192.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.170+2119_170+2122d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0127a0001c0001t0001g0143a0001c0001t0001g0170 | 3 | HG02056.hp1 HG02132.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.170+2115_170+2122d others(10): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | A | AGTGTGTG others(3): Show |
63 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0026others(60): Show | 65 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.170+2113_170+2122d others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | A | AGTGTGTG others(5): Show |
24 | a0001c0001t0001g0014a0001c0001t0001g0028a0001c0001t0001g0132others(21): Show | 25 | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.170+2111_170+2122d others(14): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | A | AGTGTGTG others(7): Show |
3 | a0001c0001t0001g0183a0001c0001t0001g0255a0001c0001t0001g0280 | 3 | HG02083.hp2 HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.170+2109_170+2122d others(16): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | A | AGTGTGTG others(9): Show |
2 | a0001c0001t0009g0125a0001c0001t0009g0239 | 2 | HG02280.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.170+2107_170+2122d others(18): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | A | AGTGTGTG others(11): Show |
2 | a0001c0001t0009g0146a0001c0001t0041g0214 | 2 | HG03195.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.170+2105_170+2122d others(20): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | AGT | A | 19 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0219others(16): Show | 20 | HG00140.hp2 HG00438.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.170+2121_170+2122d others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | AGTGT | A | 15 | a0001c0001t0001g0021a0001c0001t0001g0148a0001c0001t0001g0199others(12): Show | 16 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.170+2119_170+2122d others(6): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139544797 | AGTGTGT | A | 42 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0043others(39): Show | 46 | HG00099.hp1 HG01169.hp2 HG01175.hp1 others(43): Show |
intron_variant | MODIFIER | c.170+2117_170+2122d others(8): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139544797 | ||||||
chr4:139545086 | T | C | 2 | a0001c0001t0001g0021a0001c0001t0047g0192 | 2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.170+1834A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545086 | ||||||
chr4:139545157 | A | G | 168 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(165): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.170+1763T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545157 | ||||||
chr4:139545169 | A | G | 2 | a0001c0001t0001g0021a0001c0001t0047g0192 | 2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.170+1751T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545169 | ||||||
chr4:139545189 | CT | C | 15 | a0001c0001t0001g0014a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 16 | HG00735.hp2 HG01071.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.170+1730delA | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545189 | ||||||
chr4:139545309 | A | G | 6 | a0001c0001t0005g0008a0001c0001t0005g0062a0001c0001t0005g0063others(3): Show | 7 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+1611T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545309 | ||||||
chr4:139545355 | G | A | 1 | a0001c0001t0055g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.170+1565C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545355 | ||||||
chr4:139545450 | C | T | 98 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(95): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.170+1470G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545450 | ||||||
chr4:139545610 | A | G | 1 | a0001c0001t0027g0049 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.170+1310T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545610 | ||||||
chr4:139545613 | C | T | 171 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(168): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.170+1307G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545613 | ||||||
chr4:139545695 | C | T | 2 | a0001c0001t0001g0085a0001c0001t0018g0084 | 2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.170+1225G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545695 | ||||||
chr4:139545767 | C | T | 1 | a0001c0001t0015g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.170+1153G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545767 | ||||||
chr4:139545896 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.170+1024G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545896 | ||||||
chr4:139545959 | ATGGTCAC others(16): Show |
A | 1 | a0001c0001t0016g0262 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.170+938_170+960del others(23): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545959 | ||||||
chr4:139545968 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.170+952G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139545968 | ||||||
chr4:139546077 | CAAGCGAG others(78): Show |
C | 1 | a0001c0001t0009g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.170+758_170+842del others(85): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546077 | ||||||
chr4:139546154 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.170+766T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546154 | ||||||
chr4:139546241 | A | G | 3 | a0001c0004t0001g0252a0001c0004t0012g0251a0001c0004t0033g0071 | 3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.170+679T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546241 | ||||||
chr4:139546317 | G | A | 6 | a0001c0001t0001g0179a0001c0001t0007g0177a0001c0001t0007g0178others(3): Show | 7 | HG01261.hp2 HG02145.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.170+603C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546317 | ||||||
chr4:139546394 | C | T | 2 | a0001c0001t0017g0033a0001c0001t0026g0034 | 2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.170+526G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546394 | ||||||
chr4:139546456 | T | C | 99 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(96): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.170+464A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546456 | ||||||
chr4:139546502 | C | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0207a0001c0001t0001g0240others(3): Show | 7 | HG02559.hp2 HG02922.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+418G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546502 | ||||||
chr4:139546604 | A | T | 11 | a0001c0001t0001g0043a0001c0001t0004g0185a0001c0001t0015g0212others(8): Show | 11 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.170+316T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546604 | ||||||
chr4:139546605 | TGA | T | 11 | a0001c0001t0001g0043a0001c0001t0004g0185a0001c0001t0015g0212others(8): Show | 11 | HG01192.hp1 HG02055.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.170+313_170+314del others(2): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 2/7 | chr4 | 139546605 | ||||||
chr4:139547377 | T | C | 1 | a0001c0001t0052g0042 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.41-328A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547377 | ||||||
chr4:139547382 | A | G | 99 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(96): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-333T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547382 | ||||||
chr4:139547468 | C | T | 3 | a0001c0001t0015g0212a0001c0001t0015g0242a0001c0001t0028g0215 | 3 | HG02486.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.41-419G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547468 | ||||||
chr4:139547547 | A | G | 1 | a0001c0001t0016g0262 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-498T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547547 | ||||||
chr4:139547548 | T | A | 1 | a0001c0001t0016g0262 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-499A>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547548 | ||||||
chr4:139547554 | A | T | 1 | a0001c0001t0017g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.41-505T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547554 | ||||||
chr4:139547583 | T | G | 1 | a0001c0001t0016g0262 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-534A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547583 | ||||||
chr4:139547589 | C | A | 1 | a0001c0001t0016g0262 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-540G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547589 | ||||||
chr4:139547590 | C | G | 1 | a0001c0001t0016g0262 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-541G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547590 | ||||||
chr4:139547593 | T | TGATGGAT others(25): Show |
1 | a0001c0001t0016g0262 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-545_41-544insCG others(30): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547593 | ||||||
chr4:139547634 | A | C | 1 | a0001c0001t0016g0262 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41-585T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547634 | ||||||
chr4:139547895 | A | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0234a0001c0001t0004g0233 | 3 | HG02615.hp1 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41-846T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139547895 | ||||||
chr4:139548216 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.41-1167T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548216 | ||||||
chr4:139548236 | T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.41-1187A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548236 | ||||||
chr4:139548459 | C | T | 99 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(96): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-1410G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548459 | ||||||
chr4:139548501 | G | A | 1 | a0001c0001t0029g0190 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.41-1452C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548501 | ||||||
chr4:139548567 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.41-1518C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139548567 | ||||||
chr4:139549058 | T | G | 124 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(121): Show | 129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.41-2009A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549058 | ||||||
chr4:139549115 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.41-2066G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549115 | ||||||
chr4:139549451 | G | T | 99 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0017others(96): Show | 102 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.41-2402C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549451 | ||||||
chr4:139549460 | T | C | 14 | a0001c0001t0001g0074a0001c0001t0001g0213a0001c0001t0001g0246others(11): Show | 15 | HG00099.hp1 HG00323.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.41-2411A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549460 | ||||||
chr4:139549512 | A | ATTCCTTC others(5): Show |
25 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0147others(22): Show | 27 | HG00140.hp2 HG00438.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.41-2475_41-2464dup others(12): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | ||||||
chr4:139549512 | A | ATTCCTTC others(9): Show |
1 | a0001c0001t0009g0146 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.41-2479_41-2464dup others(16): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | ||||||
chr4:139549512 | A | ATTCCTTC others(13): Show |
42 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0028others(39): Show | 44 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.41-2464_41-2463ins others(20): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | ||||||
chr4:139549512 | A | ATTCCTTC others(17): Show |
52 | a0001c0001t0001g0015a0001c0001t0001g0026a0001c0001t0001g0040others(49): Show | 53 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.41-2464_41-2463ins others(24): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | ||||||
chr4:139549512 | A | ATTCCTTC others(21): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0254a0001c0001t0029g0190 | 3 | HG03834.hp1 NA18950.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.41-2464_41-2463ins others(28): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | ||||||
chr4:139549512 | A | ATTCCTTC others(29): Show |
1 | a0001c0001t0001g0275 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.41-2464_41-2463ins others(36): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549512 | ||||||
chr4:139549581 | C | T | 2 | a0001c0001t0017g0033a0001c0001t0026g0034 | 2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.41-2532G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549581 | ||||||
chr4:139549616 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.41-2567T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549616 | ||||||
chr4:139549682 | T | C | 1 | a0001c0001t0055g0232 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.41-2633A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549682 | ||||||
chr4:139549747 | G | C | 3 | a0001c0004t0001g0252a0001c0004t0012g0251a0001c0004t0033g0071 | 3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41-2698C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549747 | ||||||
chr4:139549774 | TA | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0126a0001c0001t0001g0203others(2): Show | 6 | HG02145.hp1 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-2726delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549774 | ||||||
chr4:139549785 | A | T | 2 | a0001c0001t0001g0079a0001c0001t0021g0080 | 2 | NA18977.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.41-2736T>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549785 | ||||||
chr4:139549892 | C | CTCCACCC others(77): Show |
1 | a0001c0001t0009g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.41-2844_41-2843ins others(84): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549892 | ||||||
chr4:139549907 | A | C | 1 | a0001c0001t0009g0125 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.41-2858T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549907 | ||||||
chr4:139549972 | G | A | 3 | a0001c0001t0001g0016a0001c0001t0011g0188a0001c0001t0011g0189 | 4 | HG02109.hp1 HG02559.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-2923C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139549972 | ||||||
chr4:139550094 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.41-3045T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550094 | ||||||
chr4:139550143 | T | C | 24 | a0001c0001t0001g0016a0001c0001t0001g0074a0001c0001t0001g0179others(21): Show | 27 | HG00099.hp1 HG00323.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.41-3094A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550143 | ||||||
chr4:139550165 | C | G | 6 | a0001c0001t0005g0008a0001c0001t0005g0062a0001c0001t0005g0063others(3): Show | 7 | HG01361.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.41-3116G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550165 | ||||||
chr4:139550370 | A | G | 2 | a0001c0001t0001g0021a0001c0001t0047g0192 | 2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.41-3321T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550370 | ||||||
chr4:139550396 | T | C | 174 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(171): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.41-3347A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550396 | ||||||
chr4:139550909 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.41-3860A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139550909 | ||||||
chr4:139551000 | C | G | 3 | a0001c0004t0001g0252a0001c0004t0012g0251a0001c0004t0033g0071 | 3 | HG02717.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41-3951G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551000 | ||||||
chr4:139551032 | A | G | 6 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202others(3): Show | 6 | HG02055.hp1 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-3983T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551032 | ||||||
chr4:139551127 | G | A | 180 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(177): Show | 189 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.41-4078C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551127 | ||||||
chr4:139551299 | A | G | 2 | a0001c0001t0001g0021a0001c0001t0047g0192 | 2 | HG04184.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.41-4250T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551299 | ||||||
chr4:139551402 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.41-4353T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551402 | ||||||
chr4:139551524 | A | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(1): Show | 4 | HG01433.hp1 HG01516.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-4475T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551524 | ||||||
chr4:139551579 | A | C | 1 | a0001c0001t0002g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.40+4519T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551579 | ||||||
chr4:139551640 | G | GAGCTGAC others(163): Show |
1 | a0001c0001t0011g0189 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.40+4457_40+4458ins others(170): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551640 | ||||||
chr4:139551737 | T | C | 1 | a0001c0001t0014g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40+4361A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551737 | ||||||
chr4:139551742 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.40+4356G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551742 | ||||||
chr4:139551743 | G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01257.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.40+4355C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551743 | ||||||
chr4:139551836 | C | G | 4 | a0001c0001t0055g0232a0001c0004t0001g0252a0001c0004t0012g0251others(1): Show | 4 | HG02717.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+4262G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551836 | ||||||
chr4:139551841 | T | C | 1 | a0001c0001t0041g0214 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.40+4257A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551841 | ||||||
chr4:139551853 | A | C | 1 | a0001c0001t0056g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.40+4245T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551853 | ||||||
chr4:139551897 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.40+4201C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139551897 | ||||||
chr4:139552045 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.40+4053C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552045 | ||||||
chr4:139552052 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.40+4046G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552052 | ||||||
chr4:139552077 | A | C | 6 | a0001c0001t0004g0185a0001c0001t0015g0242a0001c0001t0028g0215others(3): Show | 6 | HG02486.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+4021T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552077 | ||||||
chr4:139552132 | G | A | 99 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0041others(96): Show | 104 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.40+3966C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552132 | ||||||
chr4:139552209 | G | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0243others(3): Show | 7 | HG02280.hp2 HG02486.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+3889C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552209 | ||||||
chr4:139552487 | G | T | 45 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0072others(42): Show | 49 | HG00280.hp2 HG00438.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.40+3611C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552487 | ||||||
chr4:139552552 | GC | G | 12 | a0001c0001t0001g0016a0001c0001t0001g0280a0001c0001t0003g0004others(9): Show | 15 | HG01192.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.40+3545delG | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552552 | ||||||
chr4:139552659 | T | C | 13 | a0001c0001t0001g0046a0001c0001t0001g0246a0001c0001t0002g0051others(10): Show | 14 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+3439A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552659 | ||||||
chr4:139552695 | C | T | 3 | a0001c0001t0012g0228a0001c0001t0012g0230a0001c0001t0057g0229 | 3 | HG02258.hp1 HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.40+3403G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552695 | ||||||
chr4:139552784 | C | T | 4 | a0001c0001t0007g0279a0001c0001t0013g0006a0001c0001t0013g0057others(1): Show | 5 | HG02145.hp2 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+3314G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552784 | ||||||
chr4:139552790 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.40+3308C>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139552790 | ||||||
chr4:139553073 | G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225 | 3 | HG00408.hp2 HG00597.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.40+3025C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553073 | ||||||
chr4:139553240 | A | G | 2 | a0001c0001t0031g0227a0001c0001t0053g0284 | 2 | HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.40+2858T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553240 | ||||||
chr4:139553260 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.40+2838A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553260 | ||||||
chr4:139553467 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.40+2631A>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553467 | ||||||
chr4:139553541 | A | G | 1 | a0001c0001t0053g0284 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.40+2557T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553541 | ||||||
chr4:139553703 | G | A | 1 | a0001c0001t0034g0226 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.40+2395C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553703 | ||||||
chr4:139553889 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.40+2209A>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553889 | ||||||
chr4:139553919 | C | G | 1 | a0001c0001t0004g0185 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.40+2179G>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139553919 | ||||||
chr4:139554846 | C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.40+1252G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139554846 | ||||||
chr4:139555060 | G | T | 87 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(84): Show | 95 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.40+1038C>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555060 | ||||||
chr4:139555121 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.40+977T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555121 | ||||||
chr4:139555182 | C | CA | 109 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(106): Show | 114 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.40+915dupT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555182 | ||||||
chr4:139555182 | CA | C | 30 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0023others(27): Show | 34 | HG00621.hp1 HG01175.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.40+915delT | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555182 | ||||||
chr4:139555182 | CAAAAAA | C | 16 | a0001c0001t0001g0021a0001c0001t0001g0043a0001c0001t0001g0045others(13): Show | 17 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.40+910_40+915delTT others(4): Show |
SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555182 | ||||||
chr4:139555186 | A | C | 5 | a0001c0001t0001g0280a0001c0001t0004g0281a0001c0001t0007g0279others(2): Show | 5 | HG02886.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+912T>G | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555186 | ||||||
chr4:139555355 | G | A | 1 | a0001c0001t0003g0247 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.40+743C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555355 | ||||||
chr4:139555438 | C | T | 20 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0026others(17): Show | 20 | HG00408.hp1 HG01106.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.40+660G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555438 | ||||||
chr4:139555477 | G | A | 32 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(29): Show | 32 | HG00280.hp2 HG00438.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+621C>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555477 | ||||||
chr4:139555493 | C | A | 6 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0290others(3): Show | 6 | HG01069.hp1 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+605G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555493 | ||||||
chr4:139555826 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.40+272T>C | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555826 | ||||||
chr4:139555977 | C | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0280a0001c0001t0001g0286others(10): Show | 14 | HG01069.hp1 HG01192.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.40+121G>T | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139555977 | ||||||
chr4:139556004 | C | T | 1 | a0001c0001t0020g0020 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.40+94G>A | SETD7 | ENSG00000145391.14 | transcript | ENST00000274031.8 | protein_coding | 1/7 | chr4 | 139556004 |