geneid | 8840 |
---|---|
ensemblid | ENSG00000104415.14 |
hgncid | 12769 |
symbol | CCN4 |
name | cellular communication network factor 4 |
refseq_nuc | NM_003882.4 |
refseq_prot | NP_003873.1 |
ensembl_nuc | ENST00000250160.11 |
ensembl_prot | ENSP00000250160.5 |
mane_status | MANE Select |
chr | chr8 |
start | 133191039 |
end | 133231690 |
strand | + |
ver | v1.2 |
region | chr8:133191039-133231690 |
region5000 | chr8:133186039-133236690 |
regionname0 | CCN4_chr8_133191039_133231690 |
regionname5000 | CCN4_chr8_133186039_133236690 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 367 | 373 | 86 | 64 | 165 | 16 | 40 | 128 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0002 | 0/0 | 367 | 8 | 5 | 1 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0003 | 0/0 | 367 | 7 | 0 | 6 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0004 | 0/0 | 367 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0005 | 0/0 | 367 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0006 | 0/0 | 367 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0007 | 0/0 | 367 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0008 | 0/0 | 367 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1104 | 274 | 51 | 42 | 141 | 9 | 30 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0002 | 0/1 | 1104 | 71 | 19 | 21 | 13 | 7 | 10 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0003 | 0/0 | 1104 | 9 | 9 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0004 | 0/0 | 1104 | 8 | 5 | 1 | 0 | 2 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0005 | 0/0 | 1104 | 8 | 0 | 0 | 8 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0006 | 0/0 | 1104 | 5 | 0 | 4 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0007 | 0/0 | 1104 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0008 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0009 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0010 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0011 | 0/0 | 1104 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0012 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0013 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0014 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0015 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0016 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0017 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0018 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0019 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0020 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
c0021 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4087 | 193 | 22 | 26 | 111 | 7 | 27 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0002 | 0/0 | 4087 | 71 | 5 | 18 | 43 | 1 | 4 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0003 | 0/1 | 4087 | 47 | 2 | 16 | 12 | 6 | 10 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0004 | 0/0 | 4087 | 14 | 9 | 2 | 0 | 3 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0005 | 0/0 | 4087 | 8 | 7 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0006 | 0/0 | 4087 | 7 | 7 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0007 | 1/0 | 4087 | 5 | 3 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0008 | 0/0 | 4087 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0009 | 0/0 | 4087 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0010 | 0/0 | 4087 | 4 | 3 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0011 | 0/0 | 4087 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0012 | 0/0 | 4087 | 3 | 2 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0013 | 0/0 | 4087 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0014 | 0/0 | 4087 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0015 | 0/0 | 4087 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0016 | 0/0 | 4087 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0017 | 0/0 | 4087 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0018 | 0/0 | 4087 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0019 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0020 | 0/0 | 4087 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0021 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0022 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0023 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0024 | 0/0 | 4071 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0025 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0026 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0027 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0028 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0029 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0030 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0031 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0032 | 0/0 | 4087 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0033 | 0/0 | 4087 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0034 | 0/0 | 4087 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0035 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0036 | 0/0 | 4087 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0037 | 0/0 | 4087 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
t0038 | 0/0 | 4087 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1104 | 274 | 51 | 42 | 141 | 9 | 30 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002 | 0/1 | 1104 | 71 | 19 | 21 | 13 | 7 | 10 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0003 | 0/0 | 1104 | 9 | 9 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0005 | 0/0 | 1104 | 8 | 0 | 0 | 8 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0009 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0010 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0012 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0014 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0015 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0016 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0018 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0020 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0002c0004 | 0/0 | 1104 | 8 | 5 | 1 | 0 | 2 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0003c0006 | 0/0 | 1104 | 5 | 0 | 4 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0003c0007 | 0/0 | 1104 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0004c0008 | 0/0 | 1104 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0004c0019 | 0/0 | 1104 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0005c0011 | 0/0 | 1104 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0006c0021 | 0/0 | 1104 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0007c0017 | 0/0 | 1104 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0008c0013 | 0/0 | 1104 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5190 | 168 | 15 | 20 | 101 | 7 | 25 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0002 | 0/0 | 5190 | 67 | 5 | 18 | 39 | 1 | 4 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0005 | 0/0 | 5190 | 7 | 6 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0006 | 0/0 | 5190 | 7 | 7 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0007 | 1/0 | 5190 | 5 | 3 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0008 | 0/0 | 5190 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0009 | 0/0 | 5190 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0013 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0016 | 0/0 | 5190 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0019 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0020 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0022 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0023 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0024 | 0/0 | 5174 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0026 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0035 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0036 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0001t0038 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0003 | 0/1 | 5190 | 47 | 2 | 16 | 12 | 6 | 10 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0004 | 0/0 | 5190 | 5 | 3 | 1 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0010 | 0/0 | 5190 | 4 | 3 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0011 | 0/0 | 5190 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0012 | 0/0 | 5190 | 3 | 2 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0018 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0021 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0028 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0030 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0032 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0033 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0002t0034 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0003t0001 | 0/0 | 5190 | 4 | 4 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0003t0005 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0003t0014 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0003t0015 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0005t0001 | 0/0 | 5190 | 8 | 0 | 0 | 8 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0009t0004 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0009t0025 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0010t0027 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0010t0031 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0012t0001 | 0/0 | 5190 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0014t0001 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0015t0002 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0016t0013 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0018t0002 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0001c0020t0001 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0002c0004t0004 | 0/0 | 5190 | 8 | 5 | 1 | 0 | 2 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0003c0006t0001 | 0/0 | 5190 | 5 | 0 | 4 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0003c0007t0017 | 0/0 | 5190 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0004c0008t0029 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0004c0008t0037 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0004c0019t0001 | 0/0 | 5190 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0005c0011t0002 | 0/0 | 5190 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0006c0021t0001 | 0/0 | 5190 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0007c0017t0001 | 0/0 | 5190 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
a0008c0013t0001 | 0/0 | 5190 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | copy fasta | chr8 | 133186039 | 133236690 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0006g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0006g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0007g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0009g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0009g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0013g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0016g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0016g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0019g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0020g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0022g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0023g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0024g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0026g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0035g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0036g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0001t0038g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0003g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0010g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0010g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0011g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0011g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0011g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0012g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0012g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0018g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0018g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0021g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0028g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0030g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0032g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0033g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0002t0034g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0014g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0015g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0003t0015g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0005t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0005t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0005t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0005t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0005t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0009t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0009t0025g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0010t0027g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0010t0031g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0012t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0012t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0014t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0015t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0016t0013g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0018t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0001c0020t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0002c0004t0004g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0002c0004t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0002c0004t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0002c0004t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0002c0004t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0002c0004t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0002c0004t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0003c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0003c0006t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0003c0006t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0003c0006t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0003c0006t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0003c0007t0017g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0003c0007t0017g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0004c0008t0029g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0004c0008t0037g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0004c0019t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0005c0011t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0006c0021t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0007c0017t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
a0008c0013t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0187 | EUR | GBR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | GBR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00140 | hp2 | a0002 | c0004 | t0004 | g0223 | EUR | GBR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00280 | hp1 | a0002 | c0004 | t0004 | g0089 | EUR | FIN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0056 | EUR | FIN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00323 | hp1 | a0001 | c0002 | t0003 | g0084 | EUR | FIN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | FIN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00423 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00438 | hp2 | a0001 | c0005 | t0001 | g0182 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0357 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0339 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00639 | hp2 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00642 | hp2 | a0003 | c0006 | t0001 | g0045 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0370 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00735 | hp1 | a0001 | c0001 | t0016 | g0060 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00735 | hp2 | a0001 | c0002 | t0032 | g0202 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0367 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00741 | hp1 | a0001 | c0002 | t0003 | g0195 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01069 | hp1 | a0007 | c0017 | t0001 | g0059 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01070 | hp1 | a0003 | c0007 | t0017 | g0124 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01070 | hp2 | a0001 | c0002 | t0003 | g0152 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01106 | hp1 | a0001 | c0001 | t0020 | g0042 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01109 | hp2 | a0001 | c0002 | t0010 | g0269 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01167 | hp2 | a0001 | c0002 | t0012 | g0363 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01168 | hp1 | a0003 | c0006 | t0001 | g0070 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01168 | hp2 | a0001 | c0002 | t0003 | g0144 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01169 | hp2 | a0003 | c0006 | t0001 | g0066 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01175 | hp1 | a0001 | c0001 | t0016 | g0123 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01175 | hp2 | a0001 | c0002 | t0003 | g0191 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01192 | hp1 | a0003 | c0006 | t0001 | g0214 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01255 | hp2 | a0001 | c0002 | t0003 | g0147 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01358 | hp1 | a0001 | c0002 | t0004 | g0082 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0048 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01433 | hp1 | a0001 | c0002 | t0003 | g0083 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0011 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01515 | hp1 | a0001 | c0001 | t0007 | g0118 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01516 | hp2 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0008 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0093 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0348 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01891 | hp2 | a0001 | c0001 | t0022 | g0283 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01981 | hp1 | a0001 | c0014 | t0001 | g0327 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02004 | hp1 | a0001 | c0002 | t0033 | g0328 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02004 | hp2 | a0003 | c0007 | t0017 | g0242 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02040 | hp1 | a0001 | c0015 | t0002 | g0295 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02040 | hp2 | a0006 | c0021 | t0001 | g0132 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02055 | hp2 | a0001 | c0010 | t0031 | g0366 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0052 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02145 | hp2 | a0001 | c0002 | t0004 | g0109 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | CDX | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | CDX | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | CDX | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CDX | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02257 | hp1 | a0001 | c0002 | t0018 | g0232 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0100 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0110 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02258 | hp2 | a0001 | c0001 | t0035 | g0246 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0243 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0341 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02280 | hp1 | a0001 | c0002 | t0010 | g0262 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0347 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02293 | hp1 | a0001 | c0002 | t0003 | g0011 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02293 | hp2 | a0001 | c0002 | t0003 | g0127 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02300 | hp2 | a0002 | c0004 | t0004 | g0074 | AMR | PEL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02451 | hp1 | a0001 | c0001 | t0023 | g0271 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02451 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02523 | hp1 | a0001 | c0002 | t0034 | g0305 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02572 | hp1 | a0004 | c0008 | t0029 | g0108 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0277 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0194 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02615 | hp1 | a0001 | c0001 | t0026 | g0234 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0280 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02622 | hp1 | a0001 | c0002 | t0004 | g0103 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02622 | hp2 | a0001 | c0002 | t0021 | g0043 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0235 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02647 | hp2 | a0001 | c0002 | t0011 | g0266 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0029 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02698 | hp2 | a0001 | c0002 | t0003 | g0077 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02717 | hp1 | a0001 | c0002 | t0011 | g0250 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02717 | hp2 | a0001 | c0012 | t0001 | g0067 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02738 | hp1 | a0001 | c0002 | t0003 | g0369 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02738 | hp2 | a0001 | c0001 | t0036 | g0125 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0153 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02809 | hp2 | a0001 | c0002 | t0011 | g0237 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0143 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0159 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02886 | hp2 | a0001 | c0009 | t0004 | g0238 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02896 | hp1 | a0001 | c0002 | t0011 | g0265 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02896 | hp2 | a0001 | c0001 | t0009 | g0078 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0079 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0251 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02922 | hp1 | a0001 | c0012 | t0001 | g0364 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02965 | hp1 | a0001 | c0010 | t0027 | g0275 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02965 | hp2 | a0001 | c0001 | t0024 | g0255 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0281 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02970 | hp2 | a0001 | c0001 | t0019 | g0098 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02976 | hp2 | a0001 | c0003 | t0015 | g0259 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03017 | hp1 | a0003 | c0006 | t0001 | g0030 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03041 | hp1 | a0001 | c0002 | t0012 | g0106 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03130 | hp1 | a0001 | c0002 | t0010 | g0261 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0371 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0274 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03139 | hp2 | a0002 | c0004 | t0004 | g0080 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03195 | hp1 | a0004 | c0008 | t0037 | g0107 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03195 | hp2 | a0001 | c0002 | t0018 | g0041 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03209 | hp1 | a0001 | c0003 | t0014 | g0076 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03225 | hp1 | a0001 | c0002 | t0012 | g0094 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0122 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0197 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0154 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0253 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0353 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03490 | hp2 | a0001 | c0002 | t0003 | g0128 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03491 | hp1 | a0001 | c0002 | t0003 | g0032 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0354 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03516 | hp1 | a0001 | c0002 | t0004 | g0276 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03540 | hp2 | a0001 | c0003 | t0014 | g0346 | AFR | GWD | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03579 | hp1 | a0001 | c0016 | t0013 | g0270 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0362 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03669 | hp2 | a0001 | c0002 | t0003 | g0177 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0069 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03704 | hp1 | a0001 | c0002 | t0003 | g0196 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03710 | hp2 | a0008 | c0013 | t0001 | g0373 | SAS | PJL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03831 | hp1 | a0001 | c0002 | t0003 | g0200 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0360 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0149 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0264 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18522 | hp2 | a0002 | c0004 | t0004 | g0004 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | CHB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18906 | hp1 | a0001 | c0003 | t0015 | g0260 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18906 | hp2 | a0002 | c0004 | t0004 | g0359 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18946 | hp2 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18950 | hp1 | a0001 | c0018 | t0002 | g0165 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18956 | hp2 | a0001 | c0005 | t0001 | g0181 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18961 | hp1 | a0001 | c0005 | t0001 | g0179 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0337 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18978 | hp1 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18979 | hp1 | a0001 | c0002 | t0003 | g0324 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18982 | hp1 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18983 | hp1 | a0001 | c0005 | t0001 | g0180 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18983 | hp2 | a0001 | c0005 | t0001 | g0136 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18985 | hp1 | a0005 | c0011 | t0002 | g0006 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18993 | hp1 | a0001 | c0005 | t0001 | g0183 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0207 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0374 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19003 | hp1 | a0005 | c0011 | t0002 | g0006 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19030 | hp1 | a0001 | c0003 | t0005 | g0233 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19030 | hp2 | a0001 | c0009 | t0025 | g0248 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0247 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19043 | hp2 | a0001 | c0002 | t0030 | g0087 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19067 | hp2 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19070 | hp2 | a0001 | c0020 | t0001 | g0361 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19074 | hp1 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19077 | hp2 | a0001 | c0001 | t0038 | g0208 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19084 | hp1 | a0001 | c0005 | t0001 | g0010 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19240 | hp1 | a0001 | c0002 | t0010 | g0282 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | YRI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0368 | AFR | ASW | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ASW | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0091 | EUR | TSI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | TSI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0088 | EUR | TSI | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01123 | hp1 | a0001 | c0002 | t0003 | g0058 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02486 | hp1 | a0002 | c0004 | t0004 | g0046 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02486 | hp2 | a0001 | c0002 | t0028 | g0236 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0254 | AFR | ACB | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03471 | hp1 | a0004 | c0019 | t0001 | g0273 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0278 | AFR | MSL | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | USA | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | LWK | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0049 | REF | REF | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0167 | REF | REF | CCN4_chr8_133186039_133236690 | CCN4 | chr8 | 133186039 | 133236690 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:133191212
|
C | T | 1 | a0006 | 1 | HG02040.hp2 | missense_variant&splice_region_variant | MODERATE | c.68C>T | p.Thr23Met | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/5 | 174/5190 | 68/1104 | 23/367 | chr8 | 133191212 | ||
chr8:133220665
|
C | T | 1 | a0007 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.434C>T | p.Thr145Met | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 540/5190 | 434/1104 | 145/367 | chr8 | 133220665 | ||
chr8:133220680
|
C | T | 1 | a0005 | 2 | NA18985.hp1 NA19003.hp1 |
missense_variant | MODERATE | c.449C>T | p.Ala150Val | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 555/5190 | 449/1104 | 150/367 | chr8 | 133220680 | ||
chr8:133220707
|
G | A | 1 | a0008 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.476G>A | p.Arg159Gln | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 582/5190 | 476/1104 | 159/367 | chr8 | 133220707 | ||
chr8:133220781
|
G | A | 1 | a0003 | 7 | HG00642.hp2 HG01070.hp1 HG01168.hp1 others(4): Show |
missense_variant | MODERATE | c.550G>A | p.Val184Ile | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 656/5190 | 550/1104 | 184/367 | chr8 | 133220781 | ||
chr8:133220796
|
G | A | 1 | a0004 | 3 | HG02572.hp1 HG03195.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.565G>A | p.Ala189Thr | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 671/5190 | 565/1104 | 189/367 | chr8 | 133220796 | ||
chr8:133225392
|
G | T | 1 | a0002 | 8 | HG00140.hp2 HG00280.hp1 HG02300.hp2 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.613G>T | p.Ala205Ser | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/5 | 719/5190 | 613/1104 | 205/367 | chr8 | 133225392 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:133212878
|
C | T | 1 | a0001c0020 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.84C>T | p.Ala28Ala | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 190/5190 | 84/1104 | 28/367 | chr8 | 133212878 | ||
chr8:133212917
|
C | T | 1 | a0004c0019 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.123C>T | p.Asp41Asp | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 229/5190 | 123/1104 | 41/367 | chr8 | 133212917 | ||
chr8:133212935
|
A | G | 1 | a0001c0018 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.141A>G | p.Gln47Gln | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 247/5190 | 141/1104 | 47/367 | chr8 | 133212935 | ||
chr8:133212980
|
C | T | 1 | a0001c0005 | 8 | HG00438.hp2 NA18946.hp2 NA18956.hp2 others(5): Show |
synonymous_variant | LOW | c.186C>T | p.Cys62Cys | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 292/5190 | 186/1104 | 62/367 | chr8 | 133212980 | ||
chr8:133213085
|
G | A | 1 | a0001c0003 | 9 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
synonymous_variant | LOW | c.291G>A | p.Arg97Arg | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 397/5190 | 291/1104 | 97/367 | chr8 | 133213085 | ||
chr8:133213091
|
C | T | 1 | a0001c0012 | 2 | HG02717.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.297C>T | p.Leu99Leu | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/5 | 403/5190 | 297/1104 | 99/367 | chr8 | 133213091 | ||
chr8:133220789
|
G | A | 1 | a0001c0014 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.558G>A | p.Glu186Glu | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 664/5190 | 558/1104 | 186/367 | chr8 | 133220789 | ||
chr8:133220795
|
C | T | 1 | a0001c0016 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.564C>T | p.Asp188Asp | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/5 | 670/5190 | 564/1104 | 188/367 | chr8 | 133220795 | ||
chr8:133227461
|
C | T | 1 | a0001c0010 | 2 | HG02055.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.855C>T | p.Phe285Phe | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 961/5190 | 855/1104 | 285/367 | chr8 | 133227461 | ||
chr8:133227470
|
G | A | 1 | a0001c0009 | 2 | HG02886.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.864G>A | p.Ala288Ala | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 970/5190 | 864/1104 | 288/367 | chr8 | 133227470 | ||
chr8:133227503
|
G | A | 1 | a0001c0015 | 1 | HG02040.hp1 | synonymous_variant | LOW | c.897G>A | p.Lys299Lys | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1003/5190 | 897/1104 | 299/367 | chr8 | 133227503 | ||
chr8:133227527
|
T | C | 6 | a0001c0002a0001c0009a0001c0010others(3): Show | 87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
synonymous_variant | LOW | c.921T>C | p.Asn307Asn | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1027/5190 | 921/1104 | 307/367 | chr8 | 133227527 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:133191061
|
C | T | 1 | a0001c0001t0038 | 1 | NA19077.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-84C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/5 | chr8 | 133191061 | ||||||
chr8:133191093
|
G | C | 1 | a0001c0001t0019 | 1 | HG02970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-52G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/5 | 52 | chr8 | 133191093 | |||||
chr8:133191098
|
G | A | 2 | a0001c0001t0020a0001c0002t0021 | 2 | HG01106.hp1 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-47G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/5 | 47 | chr8 | 133191098 | |||||
chr8:133227971
|
C | T | 1 | a0004c0008t0037 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*261C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 261 | chr8 | 133227971 | |||||
chr8:133228161
|
C | T | 2 | a0001c0002t0010a0001c0002t0011 | 8 | HG01109.hp2 HG02280.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 451 | chr8 | 133228161 | |||||
chr8:133228351
|
G | A | 2 | a0001c0001t0013a0001c0016t0013 | 2 | HG03579.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*641G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 641 | chr8 | 133228351 | |||||
chr8:133228454
|
G | A | 47 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(44): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*744G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 744 | chr8 | 133228454 | |||||
chr8:133228680
|
C | T | 4 | a0001c0002t0003a0001c0002t0032a0001c0002t0033others(1): Show | 50 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*970C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 970 | chr8 | 133228680 | |||||
chr8:133228695
|
G | C | 1 | a0001c0002t0010 | 4 | HG01109.hp2 HG02280.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*985G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 985 | chr8 | 133228695 | |||||
chr8:133228843
|
C | G | 12 | a0001c0002t0010a0001c0002t0011a0001c0002t0012others(9): Show | 22 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1133C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1133 | chr8 | 133228843 | |||||
chr8:133228894
|
G | A | 28 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(25): Show | 231 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*1184G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1184 | chr8 | 133228894 | |||||
chr8:133228968
|
T | C | 1 | a0003c0007t0017 | 2 | HG01070.hp1 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1258T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1258 | chr8 | 133228968 | |||||
chr8:133228991
|
T | C | 1 | a0001c0001t0035 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1281T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1281 | chr8 | 133228991 | |||||
chr8:133229173
|
A | G | 2 | a0001c0010t0027a0001c0010t0031 | 2 | HG02055.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1463A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1463 | chr8 | 133229173 | |||||
chr8:133229227
|
C | A | 1 | a0001c0001t0022 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1517C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 1517 | chr8 | 133229227 | |||||
chr8:133229757
|
A | G | 1 | a0003c0007t0017 | 2 | HG01070.hp1 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2047A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2047 | chr8 | 133229757 | |||||
chr8:133229790
|
C | T | 29 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(26): Show | 232 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2080C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2080 | chr8 | 133229790 | |||||
chr8:133230093
|
G | T | 2 | a0001c0002t0010a0001c0002t0011 | 8 | HG01109.hp2 HG02280.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2383G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2383 | chr8 | 133230093 | |||||
chr8:133230095
|
T | G | 1 | a0001c0002t0028 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2385T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2385 | chr8 | 133230095 | |||||
chr8:133230108
|
G | A | 1 | a0001c0001t0023 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2398G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2398 | chr8 | 133230108 | |||||
chr8:133230129
|
C | G | 46 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(43): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*2419C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2419 | chr8 | 133230129 | |||||
chr8:133230160
|
T | C | 1 | a0001c0009t0025 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2450T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2450 | chr8 | 133230160 | |||||
chr8:133230212
|
G | A | 29 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(26): Show | 232 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*2502G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2502 | chr8 | 133230212 | |||||
chr8:133230265
|
G | T | 48 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(45): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
3_prime_UTR_variant | MODIFIER | c.*2555G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2555 | chr8 | 133230265 | |||||
chr8:133230437
|
T | G | 1 | a0001c0001t0006 | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2727T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2727 | chr8 | 133230437 | |||||
chr8:133230557
|
T | C | 1 | a0001c0001t0036 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2847T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2847 | chr8 | 133230557 | |||||
chr8:133230566
|
T | C | 53 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(50): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
3_prime_UTR_variant | MODIFIER | c.*2856T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2856 | chr8 | 133230566 | |||||
chr8:133230681
|
A | G | 1 | a0001c0001t0016 | 2 | HG00735.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2971A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 2971 | chr8 | 133230681 | |||||
chr8:133230713
|
C | G | 1 | a0001c0001t0008 | 4 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3003C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3003 | chr8 | 133230713 | |||||
chr8:133231005
|
C | T | 5 | a0001c0002t0012a0001c0002t0018a0001c0002t0021others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3295C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3295 | chr8 | 133231005 | |||||
chr8:133231024
|
C | T | 1 | a0001c0002t0033 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3314C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3314 | chr8 | 133231024 | |||||
chr8:133231113
|
T | G | 1 | a0001c0002t0018 | 2 | HG02257.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3403T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3403 | chr8 | 133231113 | |||||
chr8:133231123
|
G | C | 8 | a0001c0001t0005a0001c0001t0019a0001c0001t0020others(5): Show | 15 | HG01074.hp1 HG01106.hp1 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3413G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3413 | chr8 | 133231123 | |||||
chr8:133231127
|
GACATGAT others(9): Show |
G | 1 | a0001c0001t0024 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3418_*3433delACAT others(12): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3418 | chr8 | 133231127 | |||||
chr8:133231179
|
A | T | 1 | a0001c0003t0015 | 2 | HG02976.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3469A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3469 | chr8 | 133231179 | |||||
chr8:133231186
|
A | G | 5 | a0001c0002t0012a0001c0002t0018a0001c0002t0021others(2): Show | 8 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3476A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3476 | chr8 | 133231186 | |||||
chr8:133231225
|
T | G | 1 | a0001c0003t0014 | 2 | HG03209.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3515T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3515 | chr8 | 133231225 | |||||
chr8:133231242
|
T | C | 1 | a0001c0002t0032 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3532T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3532 | chr8 | 133231242 | |||||
chr8:133231288
|
C | G | 1 | a0001c0001t0020 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3578C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3578 | chr8 | 133231288 | |||||
chr8:133231307
|
C | T | 31 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(28): Show | 235 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*3597C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3597 | chr8 | 133231307 | |||||
chr8:133231596
|
A | G | 4 | a0001c0002t0012a0001c0002t0018a0001c0002t0021others(1): Show | 7 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3886A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 5/5 | 3886 | chr8 | 133231596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:133191340
|
C | T | 1 | a0001c0001t0002g0374 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.69+127C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191340 | ||||||
chr8:133191601
|
C | T | 1 | a0008c0013t0001g0373 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.69+388C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191601 | ||||||
chr8:133191778
|
A | T | 2 | a0001c0001t0001g0371a0001c0001t0001g0372 | 2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.69+565A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191778 | ||||||
chr8:133191793
|
G | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(74): Show | 81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.69+580G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191793 | ||||||
chr8:133191819
|
AG | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0371others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+607delG | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191819 | ||||||
chr8:133191982
|
C | T | 1 | a0001c0002t0003g0370 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.69+769C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133191982 | ||||||
chr8:133192215
|
A | G | 83 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(80): Show | 87 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.69+1002A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192215 | ||||||
chr8:133192328
|
C | A | 2 | a0001c0001t0005g0096a0001c0001t0005g0097 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.69+1115C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192328 | ||||||
chr8:133192357
|
G | T | 6 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0371others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+1144G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192357 | ||||||
chr8:133192359
|
C | T | 1 | a0001c0002t0003g0369 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.69+1146C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192359 | ||||||
chr8:133192396
|
C | T | 1 | a0001c0001t0002g0368 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+1183C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192396 | ||||||
chr8:133192549
|
A | T | 1 | a0001c0002t0003g0367 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.69+1336A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192549 | ||||||
chr8:133192581
|
T | G | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+1368T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192581 | ||||||
chr8:133192620
|
G | A | 1 | a0001c0001t0019g0098 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.69+1407G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192620 | ||||||
chr8:133192660
|
C | T | 1 | a0001c0010t0031g0366 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69+1447C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192660 | ||||||
chr8:133192685
|
A | G | 1 | a0001c0002t0004g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.69+1472A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192685 | ||||||
chr8:133192733
|
G | T | 1 | a0001c0001t0001g0365 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.69+1520G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192733 | ||||||
chr8:133192739
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.69+1526G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192739 | ||||||
chr8:133192798
|
T | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(71): Show | 78 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+1585T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192798 | ||||||
chr8:133192805
|
C | A | 1 | a0001c0001t0008g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.69+1592C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192805 | ||||||
chr8:133192838
|
G | T | 1 | a0001c0001t0008g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.69+1625G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192838 | ||||||
chr8:133192858
|
G | C | 6 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0371others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+1645G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192858 | ||||||
chr8:133192936
|
C | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0371others(3): Show | 6 | HG01884.hp2 HG02818.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+1723C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192936 | ||||||
chr8:133192936
|
C | T | 1 | a0001c0001t0002g0368 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+1723C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192936 | ||||||
chr8:133192999
|
C | A | 1 | a0001c0010t0031g0366 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.69+1786C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133192999 | ||||||
chr8:133193080
|
C | T | 2 | a0001c0002t0012g0363a0001c0012t0001g0364 | 2 | HG01167.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.69+1867C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193080 | ||||||
chr8:133193130
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.69+1917G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193130 | ||||||
chr8:133193375
|
A | G | 2 | a0001c0001t0005g0096a0001c0001t0005g0097 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.69+2162A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193375 | ||||||
chr8:133193438
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.69+2225G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193438 | ||||||
chr8:133193470
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0102others(63): Show | 69 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.69+2257G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193470 | ||||||
chr8:133193564
|
A | G | 2 | a0001c0001t0005g0362a0001c0010t0031g0366 | 2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.69+2351A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193564 | ||||||
chr8:133193665
|
A | G | 1 | a0001c0020t0001g0361 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.69+2452A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193665 | ||||||
chr8:133193727
|
T | G | 1 | a0001c0001t0005g0362 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+2514T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193727 | ||||||
chr8:133193781
|
C | T | 1 | a0001c0001t0002g0360 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69+2568C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193781 | ||||||
chr8:133193896
|
G | T | 1 | a0002c0004t0004g0359 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+2683G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133193896 | ||||||
chr8:133194004
|
G | A | 7 | a0001c0001t0001g0160a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+2791G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194004 | ||||||
chr8:133194036
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(81): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.69+2823C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194036 | ||||||
chr8:133194085
|
TTCAG | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(80): Show | 87 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.69+2873_69+2876del others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194085 | ||||||
chr8:133194181
|
C | T | 1 | a0001c0001t0001g0358 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.69+2968C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194181 | ||||||
chr8:133194293
|
G | GGT | 70 | a0001c0001t0001g0007a0001c0001t0001g0095a0001c0001t0001g0101others(67): Show | 73 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.69+3092_69+3093dup others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194293 | |||||
chr8:133194307
|
G | T | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(207): Show | 219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.69+3094G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194307 | ||||||
chr8:133194308
|
T | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(207): Show | 219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.69+3095T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194308 | ||||||
chr8:133194361
|
T | G | 8 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0027others(5): Show | 8 | HG02970.hp2 NA18945.hp2 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+3148T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194361 | ||||||
chr8:133194367
|
T | G | 1 | a0001c0001t0005g0245 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.69+3154T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194367 | ||||||
chr8:133194429
|
GGTATGTG others(10): Show |
G | 1 | a0001c0003t0001g0348 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.69+3219_69+3235del others(17): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194429 | |||||
chr8:133194442
|
GGTGT | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(206): Show | 218 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.69+3237_69+3240del others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194442 | |||||
chr8:133194466
|
GGT | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(205): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.69+3267_69+3268del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194466 | |||||
chr8:133194468
|
T | A | 2 | a0001c0001t0013g0247a0001c0001t0035g0246 | 2 | HG02258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+3255T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194468 | ||||||
chr8:133194470
|
T | G | 2 | a0001c0001t0005g0249a0001c0009t0025g0248 | 2 | HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.69+3257T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194470 | ||||||
chr8:133194505
|
A | G | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.69+3292A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194505 | ||||||
chr8:133194510
|
AGTGTGGT others(14): Show |
A | 4 | a0001c0001t0001g0031a0001c0001t0002g0029a0001c0002t0003g0032others(1): Show | 4 | HG01106.hp2 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+3309_69+3329del others(21): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194510 | |||||
chr8:133194550
|
G | A | 2 | a0001c0001t0002g0034a0001c0002t0003g0033 | 2 | HG00423.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.69+3337G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194550 | ||||||
chr8:133194561
|
G | C | 1 | a0001c0002t0004g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.69+3348G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194561 | ||||||
chr8:133194647
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0009g0093 | 2 | HG01884.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.69+3434G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194647 | ||||||
chr8:133194689
|
G | GTGTGGGG others(1): Show |
38 | a0001c0001t0001g0016a0001c0001t0001g0252a0001c0001t0001g0256others(35): Show | 39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3480_69+3481ins others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194689 | |||||
chr8:133194695
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.69+3482G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194695 | ||||||
chr8:133194696
|
G | T | 38 | a0001c0001t0001g0016a0001c0001t0001g0252a0001c0001t0001g0256others(35): Show | 39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3483G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194696 | ||||||
chr8:133194699
|
G | T | 38 | a0001c0001t0001g0016a0001c0001t0001g0252a0001c0001t0001g0256others(35): Show | 39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3486G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194699 | ||||||
chr8:133194717
|
G | GTGGTGTG others(3): Show |
38 | a0001c0001t0001g0016a0001c0001t0001g0252a0001c0001t0001g0256others(35): Show | 39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3504_69+3505ins others(10): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194717 | ||||||
chr8:133194721
|
A | G | 38 | a0001c0001t0001g0016a0001c0001t0001g0252a0001c0001t0001g0256others(35): Show | 39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3508A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194721 | ||||||
chr8:133194722
|
T | G | 38 | a0001c0001t0001g0016a0001c0001t0001g0252a0001c0001t0001g0256others(35): Show | 39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3509T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194722 | ||||||
chr8:133194729
|
A | G | 38 | a0001c0001t0001g0016a0001c0001t0001g0252a0001c0001t0001g0256others(35): Show | 39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3516A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194729 | ||||||
chr8:133194730
|
G | C | 38 | a0001c0001t0001g0016a0001c0001t0001g0252a0001c0001t0001g0256others(35): Show | 39 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.69+3517G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194730 | ||||||
chr8:133194730
|
G | GTGTGTGG others(31): Show |
74 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0090others(71): Show | 78 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.69+3523_69+3524ins others(38): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194730 | |||||
chr8:133194730
|
G | GTGTGTGT others(35): Show |
98 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(95): Show | 102 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.69+3533_69+3534ins others(42): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194730 | |||||
chr8:133194774
|
G | T | 1 | a0001c0001t0005g0362 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+3561G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194774 | ||||||
chr8:133194828
|
C | T | 4 | a0001c0001t0007g0347a0001c0001t0008g0100a0001c0003t0014g0346others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+3615C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194828 | ||||||
chr8:133194837
|
G | A | 1 | a0001c0001t0005g0362 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+3624G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194837 | ||||||
chr8:133194928
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.69+3715T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194928 | ||||||
chr8:133194985
|
T | G | 1 | a0001c0001t0001g0284 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.69+3772T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133194985 | ||||||
chr8:133194995
|
TTG | T | 6 | a0001c0001t0002g0001a0001c0001t0002g0240a0001c0001t0002g0241others(3): Show | 9 | HG01074.hp2 HG01258.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+3792_69+3793del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133194995 | |||||
chr8:133195006
|
T | G | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 6 | HG02129.hp2 NA18978.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+3793T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195006 | ||||||
chr8:133195017
|
G | T | 1 | a0001c0002t0003g0032 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.69+3804G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195017 | ||||||
chr8:133195082
|
T | G | 66 | a0001c0001t0001g0007a0001c0001t0001g0101a0001c0001t0001g0102others(63): Show | 69 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.69+3869T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195082 | ||||||
chr8:133195101
|
G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0002t0003g0033 | 3 | HG00423.hp2 HG01934.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.69+3888G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195101 | ||||||
chr8:133195123
|
G | A | 5 | a0001c0001t0001g0095a0001c0001t0001g0371a0001c0001t0001g0372others(2): Show | 5 | HG01891.hp1 HG02818.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+3910G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195123 | ||||||
chr8:133195160
|
GTGTGTAT others(10): Show |
G | 1 | a0001c0001t0001g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+3964_69+3980del others(17): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133195160 | |||||
chr8:133195164
|
GTATGTGG others(36): Show |
G | 1 | a0001c0001t0001g0085 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.69+3953_69+3995del others(43): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133195164 | |||||
chr8:133195173
|
G | A | 1 | a0001c0001t0019g0098 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.69+3960G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195173 | ||||||
chr8:133195207
|
A | G | 80 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(77): Show | 82 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.69+3994A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195207 | ||||||
chr8:133195319
|
G | GGTGT | 10 | a0001c0001t0002g0239a0001c0001t0006g0235a0001c0001t0026g0234others(7): Show | 10 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+4118_69+4121dup others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133195319 | |||||
chr8:133195325
|
T | C | 1 | a0001c0001t0002g0368 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+4112T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195325 | ||||||
chr8:133195588
|
C | A | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+4375C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195588 | ||||||
chr8:133195590
|
C | T | 1 | a0001c0001t0013g0247 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.69+4377C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195590 | ||||||
chr8:133195601
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.69+4388C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195601 | ||||||
chr8:133195626
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | NA18950.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.69+4413C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195626 | ||||||
chr8:133195720
|
A | G | 27 | a0001c0001t0001g0095a0001c0001t0001g0279a0001c0001t0001g0344others(24): Show | 27 | HG00323.hp1 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.69+4507A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195720 | ||||||
chr8:133195802
|
C | A | 2 | a0001c0002t0012g0363a0001c0012t0001g0364 | 2 | HG01167.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.69+4589C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195802 | ||||||
chr8:133195869
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0175a0001c0001t0001g0176 | 4 | HG01123.hp2 HG03654.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+4656G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195869 | ||||||
chr8:133195955
|
C | T | 3 | a0001c0002t0004g0276a0001c0003t0001g0274a0001c0010t0027g0275 | 3 | HG02965.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.69+4742C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195955 | ||||||
chr8:133195963
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.69+4750C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133195963 | ||||||
chr8:133196197
|
C | G | 5 | a0001c0002t0004g0276a0001c0003t0001g0274a0001c0003t0001g0348others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+4984C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196197 | ||||||
chr8:133196246
|
C | T | 3 | a0001c0001t0001g0151a0001c0001t0002g0150a0001c0002t0003g0152 | 3 | HG00323.hp2 HG01070.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.69+5033C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196246 | ||||||
chr8:133196356
|
G | A | 1 | a0001c0001t0002g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.69+5143G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196356 | ||||||
chr8:133196438
|
T | G | 2 | a0001c0001t0001g0095a0001c0002t0012g0094 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.69+5225T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196438 | ||||||
chr8:133196512
|
G | T | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+5299G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196512 | ||||||
chr8:133196596
|
A | T | 142 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(139): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.69+5383A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196596 | ||||||
chr8:133196601
|
AAGGGTTC others(7): Show |
A | 2 | a0001c0002t0003g0083a0001c0002t0004g0082 | 2 | HG01358.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.69+5391_69+5404del others(14): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133196601 | |||||
chr8:133196643
|
CTCAGGTA others(35): Show |
C | 1 | a0001c0001t0002g0349 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.69+5432_69+5473del others(42): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133196643 | |||||
chr8:133196682
|
T | C | 4 | a0001c0002t0004g0276a0001c0003t0001g0274a0001c0003t0001g0348others(1): Show | 4 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+5469T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196682 | ||||||
chr8:133196732
|
T | G | 1 | a0001c0001t0005g0245 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.69+5519T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196732 | ||||||
chr8:133196882
|
T | C | 3 | a0001c0002t0030g0087a0001c0009t0025g0248a0002c0004t0004g0359 | 3 | NA18906.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.69+5669T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196882 | ||||||
chr8:133196906
|
T | G | 5 | a0001c0001t0002g0149a0001c0001t0005g0249a0001c0001t0013g0247others(2): Show | 5 | HG02976.hp1 HG04199.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+5693T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196906 | ||||||
chr8:133196917
|
G | A | 2 | a0001c0001t0008g0111a0001c0001t0009g0110 | 2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.69+5704G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133196917 | ||||||
chr8:133197013
|
C | T | 4 | a0001c0002t0004g0276a0001c0003t0001g0274a0001c0003t0001g0348others(1): Show | 4 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+5800C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197013 | ||||||
chr8:133197210
|
C | G | 72 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(69): Show | 77 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+5997C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197210 | ||||||
chr8:133197273
|
C | A | 1 | a0001c0002t0028g0236 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69+6060C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197273 | ||||||
chr8:133197366
|
G | A | 1 | a0001c0003t0001g0274 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.69+6153G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197366 | ||||||
chr8:133197528
|
C | G | 36 | a0001c0001t0001g0092a0001c0001t0001g0256a0001c0001t0001g0257others(33): Show | 36 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.69+6315C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197528 | ||||||
chr8:133197605
|
G | A | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.69+6392G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197605 | ||||||
chr8:133197657
|
C | A | 1 | a0001c0002t0011g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+6444C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197657 | ||||||
chr8:133197676
|
C | T | 1 | a0002c0004t0004g0223 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.69+6463C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197676 | ||||||
chr8:133197711
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+6498G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197711 | ||||||
chr8:133197914
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69+6701C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197914 | ||||||
chr8:133197952
|
T | C | 1 | a0001c0009t0025g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.69+6739T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197952 | ||||||
chr8:133197970
|
A | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(68): Show | 75 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.69+6757A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197970 | ||||||
chr8:133197988
|
C | A | 4 | a0001c0001t0001g0035a0001c0001t0005g0047a0002c0004t0004g0004others(1): Show | 5 | HG01074.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+6775C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133197988 | ||||||
chr8:133198010
|
G | A | 2 | a0001c0002t0003g0048a0001c0002t0003g0049 | 2 | HG01361.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.69+6797G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198010 | ||||||
chr8:133198229
|
C | T | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.69+7016C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198229 | ||||||
chr8:133198294
|
T | G | 1 | a0001c0002t0003g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69+7081T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198294 | ||||||
chr8:133198331
|
T | G | 3 | a0001c0001t0013g0247a0001c0001t0026g0234a0002c0004t0004g0359 | 3 | HG02615.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+7118T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198331 | ||||||
chr8:133198839
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0005g0047a0002c0004t0004g0004others(1): Show | 5 | HG01074.hp1 HG02109.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+7626C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198839 | ||||||
chr8:133198844
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.69+7631C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198844 | ||||||
chr8:133198906
|
C | T | 4 | a0001c0002t0004g0276a0001c0003t0001g0274a0001c0003t0001g0348others(1): Show | 4 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+7693C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198906 | ||||||
chr8:133198993
|
C | A | 6 | a0001c0001t0019g0098a0001c0002t0004g0276a0001c0002t0018g0232others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+7780C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198993 | ||||||
chr8:133198998
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(156): Show | 169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.69+7785C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133198998 | ||||||
chr8:133199167
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(156): Show | 169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.69+7954G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199167 | ||||||
chr8:133199283
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(157): Show | 170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.69+8070C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199283 | ||||||
chr8:133199321
|
G | A | 1 | a0001c0002t0012g0363 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.69+8108G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199321 | ||||||
chr8:133199624
|
C | T | 70 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(67): Show | 74 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.69+8411C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199624 | ||||||
chr8:133199665
|
C | T | 3 | a0001c0001t0001g0092a0001c0001t0009g0093a0001c0003t0005g0233 | 3 | HG01884.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.69+8452C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199665 | ||||||
chr8:133199704
|
A | G | 1 | a0001c0001t0002g0338 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.69+8491A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199704 | ||||||
chr8:133199711
|
C | T | 46 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0031others(43): Show | 49 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.69+8498C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199711 | ||||||
chr8:133199722
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(58): Show | 65 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.69+8509G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199722 | ||||||
chr8:133199749
|
G | C | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+8536G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199749 | ||||||
chr8:133199887
|
T | C | 74 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(71): Show | 78 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.69+8674T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199887 | ||||||
chr8:133199919
|
T | C | 9 | a0001c0001t0001g0178a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 10 | HG00438.hp2 NA18946.hp2 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+8706T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133199919 | ||||||
chr8:133200133
|
C | T | 9 | a0001c0001t0001g0095a0001c0001t0001g0224a0001c0001t0002g0342others(6): Show | 9 | HG02630.hp2 HG02886.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+8920C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200133 | ||||||
chr8:133200143
|
G | A | 46 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0031others(43): Show | 49 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.69+8930G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200143 | ||||||
chr8:133200220
|
C | T | 1 | a0002c0004t0004g0074 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.69+9007C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200220 | ||||||
chr8:133200222
|
C | T | 4 | a0001c0001t0001g0371a0001c0001t0002g0154a0001c0001t0002g0368others(1): Show | 4 | HG01891.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+9009C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200222 | ||||||
chr8:133200245
|
G | A | 2 | a0001c0001t0013g0247a0002c0004t0004g0359 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+9032G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200245 | ||||||
chr8:133200363
|
C | T | 1 | a0001c0002t0003g0177 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69+9150C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200363 | ||||||
chr8:133200409
|
C | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(60): Show | 67 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.69+9196C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200409 | ||||||
chr8:133200412
|
G | T | 1 | a0001c0001t0001g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.69+9199G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200412 | ||||||
chr8:133200486
|
G | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.69+9273G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200486 | ||||||
chr8:133200505
|
C | T | 1 | a0001c0001t0001g0355 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.69+9292C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200505 | ||||||
chr8:133200506
|
G | A | 1 | a0001c0002t0003g0056 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+9293G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200506 | ||||||
chr8:133200686
|
A | G | 2 | a0001c0001t0001g0353a0001c0001t0001g0354 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.69+9473A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200686 | ||||||
chr8:133200851
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+9638C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133200851 | ||||||
chr8:133201008
|
C | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(59): Show | 66 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.69+9795C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201008 | ||||||
chr8:133201012
|
G | C | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.69+9799G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201012 | ||||||
chr8:133201015
|
G | C | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.69+9802G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201015 | ||||||
chr8:133201021
|
T | C | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.69+9808T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201021 | ||||||
chr8:133201056
|
T | C | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+9843T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201056 | ||||||
chr8:133201060
|
C | T | 2 | a0001c0001t0001g0113a0008c0013t0001g0373 | 2 | HG01346.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.69+9847C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201060 | ||||||
chr8:133201128
|
C | T | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 219 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.69+9915C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201128 | ||||||
chr8:133201167
|
C | T | 22 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(19): Show | 22 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.69+9954C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201167 | ||||||
chr8:133201233
|
C | T | 8 | a0001c0001t0005g0245a0001c0001t0019g0098a0001c0002t0004g0276others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+10020C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201233 | ||||||
chr8:133201356
|
T | C | 36 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(33): Show | 36 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.69+10143T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201356 | ||||||
chr8:133201427
|
A | G | 6 | a0001c0001t0019g0098a0001c0002t0004g0276a0001c0002t0018g0232others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+10214A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201427 | ||||||
chr8:133201442
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(126): Show | 138 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.69+10229G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201442 | ||||||
chr8:133201447
|
G | A | 7 | a0001c0001t0001g0345a0001c0001t0005g0249a0001c0001t0006g0254others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+10234G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201447 | ||||||
chr8:133201531
|
G | A | 1 | a0001c0002t0003g0369 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.69+10318G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201531 | ||||||
chr8:133201736
|
G | A | 6 | a0001c0001t0019g0098a0001c0002t0004g0276a0001c0002t0018g0232others(3): Show | 6 | HG01891.hp1 HG02257.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+10523G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201736 | ||||||
chr8:133201742
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.69+10529C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201742 | ||||||
chr8:133201798
|
A | G | 8 | a0001c0001t0001g0345a0001c0001t0002g0149a0001c0001t0005g0249others(5): Show | 8 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+10585A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201798 | ||||||
chr8:133201803
|
A | C | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+10590A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201803 | ||||||
chr8:133201844
|
A | AAAAAG | 11 | a0001c0001t0001g0095a0001c0001t0001g0174a0001c0001t0005g0157others(8): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+10656_69+10660d others(7): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201844 | |||||
chr8:133201844
|
AAAAAG | A | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(217): Show | 233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.69+10656_69+10660d others(7): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201844 | |||||
chr8:133201844
|
AAAAAGAA others(3): Show |
A | 5 | a0001c0001t0002g0368a0001c0002t0004g0276a0001c0003t0001g0274others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+10651_69+10660d others(12): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201844 | |||||
chr8:133201864
|
G | GAAAAGAA others(1): Show |
32 | a0001c0001t0001g0092a0001c0001t0001g0256a0001c0001t0001g0257others(29): Show | 32 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.69+10656_69+10663d others(10): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201864 | |||||
chr8:133201864
|
GAAAAGA | G | 7 | a0001c0001t0001g0345a0001c0001t0005g0249a0001c0001t0006g0254others(4): Show | 7 | HG01243.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+10656_69+10661d others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133201864 | |||||
chr8:133201878
|
C | T | 9 | a0001c0001t0001g0178a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 10 | HG00438.hp2 NA18946.hp2 NA18956.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+10665C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201878 | ||||||
chr8:133201948
|
C | A | 46 | a0001c0001t0001g0020a0001c0001t0001g0031a0001c0001t0001g0035others(43): Show | 48 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.69+10735C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201948 | ||||||
chr8:133201961
|
C | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(65): Show | 72 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.69+10748C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201961 | ||||||
chr8:133201962
|
G | A | 1 | a0001c0002t0012g0363 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.69+10749G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201962 | ||||||
chr8:133201966
|
T | C | 2 | a0001c0001t0019g0098a0001c0002t0018g0232 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.69+10753T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201966 | ||||||
chr8:133201981
|
G | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(72): Show | 79 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.69+10768G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133201981 | ||||||
chr8:133202336
|
T | C | 2 | a0001c0001t0002g0349a0001c0001t0002g0356 | 2 | HG00408.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.70-10528T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202336 | ||||||
chr8:133202341
|
C | T | 1 | a0001c0002t0003g0147 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.70-10523C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202341 | ||||||
chr8:133202411
|
C | A | 1 | a0001c0001t0002g0240 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.70-10453C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202411 | ||||||
chr8:133202434
|
A | T | 2 | a0001c0001t0005g0245a0001c0002t0012g0094 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-10430A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202434 | ||||||
chr8:133202663
|
T | A | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(272): Show | 288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.70-10201T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202663 | ||||||
chr8:133202684
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.70-10180G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202684 | ||||||
chr8:133202800
|
A | G | 2 | a0001c0001t0019g0098a0001c0002t0018g0232 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.70-10064A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202800 | ||||||
chr8:133202869
|
G | A | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(142): Show | 154 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.70-9995G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202869 | ||||||
chr8:133202939
|
G | C | 2 | a0001c0001t0005g0245a0001c0002t0012g0094 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-9925G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133202939 | ||||||
chr8:133203011
|
C | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 9 | NA18612.hp1 NA18955.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-9853C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203011 | ||||||
chr8:133203241
|
C | T | 3 | a0001c0001t0001g0371a0001c0001t0002g0154a0001c0001t0022g0283 | 3 | HG01891.hp2 HG03130.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.70-9623C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203241 | ||||||
chr8:133203268
|
C | T | 3 | a0001c0001t0008g0111a0001c0001t0009g0110a0001c0012t0001g0364 | 3 | HG02258.hp1 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.70-9596C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203268 | ||||||
chr8:133203388
|
A | G | 328 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(325): Show | 345 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.70-9476A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203388 | ||||||
chr8:133203703
|
G | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(116): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.70-9161G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203703 | ||||||
chr8:133203713
|
T | A | 21 | a0001c0001t0001g0092a0001c0001t0001g0256a0001c0001t0001g0257others(18): Show | 21 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.70-9151T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203713 | ||||||
chr8:133203757
|
G | C | 163 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0012others(160): Show | 170 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.70-9107G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203757 | ||||||
chr8:133203841
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70-9023G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203841 | ||||||
chr8:133203844
|
C | T | 4 | a0001c0002t0004g0276a0001c0003t0001g0274a0001c0003t0001g0348others(1): Show | 4 | HG01891.hp1 HG02965.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-9020C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203844 | ||||||
chr8:133203953
|
A | G | 1 | a0001c0020t0001g0361 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.70-8911A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133203953 | ||||||
chr8:133204111
|
C | T | 2 | a0001c0001t0019g0098a0001c0002t0018g0232 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.70-8753C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204111 | ||||||
chr8:133204285
|
T | C | 1 | a0001c0002t0003g0193 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.70-8579T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204285 | ||||||
chr8:133204312
|
A | C | 47 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0031others(44): Show | 50 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.70-8552A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204312 | ||||||
chr8:133204354
|
G | A | 2 | a0001c0001t0019g0098a0001c0002t0018g0232 | 2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.70-8510G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204354 | ||||||
chr8:133204491
|
AG | A | 7 | a0001c0001t0001g0016a0001c0001t0005g0096a0001c0001t0005g0097others(4): Show | 8 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-8370delG | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133204491 | |||||
chr8:133204519
|
C | T | 1 | a0001c0001t0001g0028 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.70-8345C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204519 | ||||||
chr8:133204528
|
A | G | 2 | a0001c0002t0003g0048a0001c0002t0003g0049 | 2 | HG01361.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.70-8336A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204528 | ||||||
chr8:133204606
|
A | G | 329 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(326): Show | 346 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.70-8258A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204606 | ||||||
chr8:133204635
|
G | A | 1 | a0001c0002t0011g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-8229G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204635 | ||||||
chr8:133204676
|
T | A | 2 | a0001c0001t0001g0057a0002c0004t0004g0074 | 2 | HG00099.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.70-8188T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204676 | ||||||
chr8:133204955
|
G | C | 24 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(21): Show | 24 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.70-7909G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204955 | ||||||
chr8:133204956
|
G | A | 1 | a0002c0004t0004g0089 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.70-7908G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133204956 | ||||||
chr8:133205002
|
G | A | 2 | a0001c0001t0005g0245a0001c0002t0012g0094 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-7862G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205002 | ||||||
chr8:133205057
|
C | T | 1 | a0001c0009t0025g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.70-7807C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205057 | ||||||
chr8:133205107
|
G | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(5): Show | 8 | NA18945.hp2 NA18964.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-7757G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205107 | ||||||
chr8:133205144
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.70-7720G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205144 | ||||||
chr8:133205380
|
T | G | 4 | a0001c0001t0001g0371a0001c0001t0002g0154a0001c0001t0002g0368others(1): Show | 4 | HG01891.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-7484T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205380 | ||||||
chr8:133205462
|
T | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(263): Show | 281 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.70-7402T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205462 | ||||||
chr8:133205909
|
G | A | 5 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0221others(2): Show | 5 | HG00323.hp2 HG01070.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-6955G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133205909 | ||||||
chr8:133206180
|
G | A | 1 | a0001c0002t0003g0084 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.70-6684G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206180 | ||||||
chr8:133206257
|
G | A | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(151): Show | 165 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.70-6607G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206257 | ||||||
chr8:133206291
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.70-6573T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206291 | ||||||
chr8:133206292
|
G | A | 7 | a0001c0001t0001g0016a0001c0001t0005g0096a0001c0001t0005g0097others(4): Show | 8 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-6572G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206292 | ||||||
chr8:133206297
|
A | G | 301 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(298): Show | 317 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.70-6567A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206297 | ||||||
chr8:133206299
|
C | T | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0002g0117others(3): Show | 7 | HG01168.hp2 HG01255.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-6565C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206299 | ||||||
chr8:133206342
|
G | A | 1 | a0001c0001t0007g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.70-6522G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206342 | ||||||
chr8:133206357
|
G | T | 1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.70-6507G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206357 | ||||||
chr8:133206373
|
G | C | 3 | a0001c0001t0008g0111a0001c0001t0009g0110a0001c0012t0001g0364 | 3 | HG02258.hp1 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.70-6491G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206373 | ||||||
chr8:133206573
|
G | C | 9 | a0001c0001t0001g0345a0001c0001t0002g0239a0001c0001t0002g0368others(6): Show | 9 | HG01243.hp2 HG02559.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-6291G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206573 | ||||||
chr8:133206576
|
T | C | 1 | a0001c0001t0001g0371 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.70-6288T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206576 | ||||||
chr8:133206583
|
G | A | 1 | a0001c0002t0004g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.70-6281G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206583 | ||||||
chr8:133206687
|
G | C | 8 | a0001c0001t0001g0345a0001c0001t0005g0249a0001c0001t0006g0254others(5): Show | 8 | HG01243.hp2 HG02559.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-6177G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206687 | ||||||
chr8:133206790
|
A | G | 13 | a0001c0001t0001g0095a0001c0001t0005g0157a0001c0001t0005g0362others(10): Show | 13 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-6074A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206790 | ||||||
chr8:133206799
|
G | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0028others(17): Show | 20 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.70-6065G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206799 | ||||||
chr8:133206821
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.70-6043G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206821 | ||||||
chr8:133206995
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(87): Show | 97 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.70-5869G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133206995 | ||||||
chr8:133207034
|
G | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(156): Show | 170 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.70-5830G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207034 | ||||||
chr8:133207059
|
C | T | 2 | a0001c0001t0001g0345a0001c0002t0004g0103 | 2 | HG01243.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.70-5805C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207059 | ||||||
chr8:133207185
|
C | G | 1 | a0001c0001t0002g0217 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.70-5679C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207185 | ||||||
chr8:133207537
|
G | C | 1 | a0001c0001t0001g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.70-5327G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207537 | ||||||
chr8:133207561
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.70-5303C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207561 | ||||||
chr8:133207575
|
C | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0015others(64): Show | 71 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.70-5289C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207575 | ||||||
chr8:133207631
|
A | C | 6 | a0001c0001t0002g0239a0001c0001t0002g0368a0001c0001t0013g0247others(3): Show | 6 | HG02615.hp1 HG03041.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-5233A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207631 | ||||||
chr8:133207648
|
C | T | 1 | a0001c0001t0019g0098 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.70-5216C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207648 | ||||||
chr8:133207697
|
TCTC | T | 7 | a0001c0001t0001g0016a0001c0001t0005g0096a0001c0001t0005g0097others(4): Show | 8 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-5165_70-5163del others(3): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207697 | |||||
chr8:133207820
|
G | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0017others(92): Show | 102 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.70-5044G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133207820 | ||||||
chr8:133207994
|
G | GT | 6 | a0001c0001t0002g0001a0001c0001t0002g0244a0001c0002t0003g0243others(3): Show | 9 | HG00733.hp2 HG01074.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-4856dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | |||||
chr8:133207994
|
G | GTTTTTTT | 23 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0027others(20): Show | 25 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.70-4862_70-4856dup others(7): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | |||||
chr8:133207994
|
G | GTTTTTTT others(1): Show |
57 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0039others(54): Show | 62 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.70-4863_70-4856dup others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | |||||
chr8:133207994
|
G | GTTTTTTT others(2): Show |
10 | a0001c0001t0001g0216a0001c0001t0001g0323a0001c0001t0001g0326others(7): Show | 10 | HG00621.hp2 HG01981.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-4864_70-4856dup others(9): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | |||||
chr8:133207994
|
GT | G | 175 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0012others(172): Show | 185 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.70-4856delT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133207994 | |||||
chr8:133208205
|
C | G | 7 | a0001c0001t0001g0345a0001c0001t0005g0249a0001c0001t0006g0254others(4): Show | 7 | HG01243.hp2 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-4659C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208205 | ||||||
chr8:133208448
|
A | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(279): Show | 297 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.70-4416A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208448 | ||||||
chr8:133208503
|
AGGCATTC others(15): Show |
A | 1 | a0001c0001t0002g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.70-4359_70-4338del others(22): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133208503 | |||||
chr8:133208568
|
G | A | 1 | a0001c0002t0003g0088 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.70-4296G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208568 | ||||||
chr8:133208598
|
A | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 248 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.70-4266A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208598 | ||||||
chr8:133208652
|
C | T | 1 | a0001c0002t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.70-4212C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208652 | ||||||
chr8:133208669
|
G | A | 2 | a0001c0001t0005g0245a0001c0002t0012g0094 | 2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-4195G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208669 | ||||||
chr8:133208736
|
T | G | 119 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(116): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.70-4128T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208736 | ||||||
chr8:133208832
|
T | C | 4 | a0001c0001t0013g0247a0001c0001t0019g0098a0001c0002t0018g0232others(1): Show | 4 | HG02257.hp1 HG02970.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-4032T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208832 | ||||||
chr8:133208886
|
T | C | 1 | a0001c0001t0023g0271 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.70-3978T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133208886 | ||||||
chr8:133209086
|
C | T | 2 | a0001c0003t0001g0274a0001c0003t0001g0348 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.70-3778C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209086 | ||||||
chr8:133209210
|
T | C | 13 | a0001c0001t0001g0016a0001c0001t0005g0096a0001c0001t0005g0097others(10): Show | 14 | HG01167.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-3654T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209210 | ||||||
chr8:133209230
|
A | T | 231 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(228): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.70-3634A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209230 | ||||||
chr8:133209259
|
T | C | 243 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0012others(240): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.70-3605T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209259 | ||||||
chr8:133209498
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.70-3366G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209498 | ||||||
chr8:133209516
|
T | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0294a0001c0001t0001g0323others(1): Show | 4 | NA18977.hp1 NA18988.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-3348T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209516 | ||||||
chr8:133209605
|
C | T | 9 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0102others(6): Show | 10 | HG01123.hp2 HG01192.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-3259C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209605 | ||||||
chr8:133209680
|
T | C | 6 | a0001c0001t0001g0035a0001c0001t0001g0372a0001c0001t0008g0111others(3): Show | 7 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-3184T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209680 | ||||||
chr8:133209743
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0092a0001c0001t0005g0096others(1): Show | 5 | HG02109.hp2 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-3121G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209743 | ||||||
chr8:133209926
|
A | T | 1 | a0001c0002t0028g0236 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.70-2938A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209926 | ||||||
chr8:133209976
|
T | C | 24 | a0001c0001t0001g0095a0001c0001t0001g0112a0001c0001t0001g0252others(21): Show | 28 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.70-2888T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133209976 | ||||||
chr8:133210005
|
T | A | 2 | a0001c0001t0002g0150a0001c0002t0004g0082 | 2 | HG00323.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.70-2859T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210005 | ||||||
chr8:133210043
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0226a0001c0001t0002g0225 | 4 | NA18975.hp1 NA18988.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-2821T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210043 | ||||||
chr8:133210054
|
T | C | 29 | a0001c0001t0001g0222a0001c0001t0001g0263a0001c0001t0001g0272others(26): Show | 29 | HG00735.hp1 HG01069.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.70-2810T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210054 | ||||||
chr8:133210144
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(63): Show | 72 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.70-2720T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210144 | ||||||
chr8:133210144
|
T | G | 1 | a0001c0001t0002g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.70-2720T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210144 | ||||||
chr8:133210386
|
G | GGT | 19 | a0001c0001t0001g0102a0001c0001t0005g0047a0001c0001t0005g0157others(16): Show | 19 | HG00280.hp1 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.70-2443_70-2442dup others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | |||||
chr8:133210386
|
G | GGTGTGT | 9 | a0001c0001t0001g0016a0001c0001t0001g0092a0001c0001t0002g0142others(6): Show | 10 | HG02109.hp2 HG03209.hp1 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-2447_70-2442dup others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | |||||
chr8:133210386
|
G | GGTGTGTG others(3): Show |
4 | a0001c0003t0001g0153a0001c0003t0001g0274a0001c0003t0001g0277others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2451_70-2442dup others(10): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | |||||
chr8:133210386
|
GGT | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(120): Show | 130 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.70-2443_70-2442del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | |||||
chr8:133210386
|
GGTGT | G | 25 | a0001c0001t0001g0044a0001c0001t0001g0112a0001c0001t0001g0178others(22): Show | 29 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.70-2445_70-2442del others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210386 | |||||
chr8:133210407
|
G | T | 4 | a0001c0002t0004g0109a0001c0002t0012g0094a0001c0002t0012g0363others(1): Show | 4 | HG01167.hp2 HG02145.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-2457G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210407 | ||||||
chr8:133210420
|
TG | T | 6 | a0001c0001t0001g0072a0001c0001t0001g0101a0001c0001t0001g0145others(3): Show | 6 | HG00738.hp1 HG01515.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-2443delG | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210420 | ||||||
chr8:133210421
|
G | GT | 49 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(46): Show | 55 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.70-2440dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210421 | |||||
chr8:133210421
|
G | GTGT | 5 | a0001c0001t0001g0031a0001c0001t0001g0057a0001c0001t0001g0344others(2): Show | 5 | HG00099.hp1 HG01106.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-2442_70-2441ins others(3): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210421 | |||||
chr8:133210549
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70-2315T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210549 | ||||||
chr8:133210622
|
A | AT | 6 | a0001c0001t0002g0117a0001c0001t0016g0123a0001c0002t0003g0008others(3): Show | 7 | HG00639.hp2 HG01168.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-2234dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 133210622 | |||||
chr8:133210629
|
T | C | 2 | a0001c0002t0018g0232a0001c0002t0028g0236 | 2 | HG02257.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.70-2235T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210629 | ||||||
chr8:133210677
|
T | A | 1 | a0001c0001t0001g0329 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.70-2187T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210677 | ||||||
chr8:133210756
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0037 | 4 | NA18955.hp1 NA18981.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-2108G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210756 | ||||||
chr8:133210830
|
C | T | 3 | a0001c0001t0001g0102a0001c0012t0001g0067a0001c0012t0001g0364 | 3 | HG02717.hp2 HG02922.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.70-2034C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210830 | ||||||
chr8:133210915
|
T | C | 5 | a0001c0001t0006g0081a0001c0001t0006g0235a0001c0001t0006g0280others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-1949T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210915 | ||||||
chr8:133210921
|
G | A | 9 | a0001c0001t0006g0081a0001c0001t0006g0143a0001c0001t0006g0235others(6): Show | 9 | HG02559.hp2 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-1943G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210921 | ||||||
chr8:133210925
|
C | T | 7 | a0001c0003t0001g0153a0001c0003t0001g0274a0001c0003t0001g0277others(4): Show | 7 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-1939C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133210925 | ||||||
chr8:133211065
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.70-1799G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211065 | ||||||
chr8:133211195
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.70-1669A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211195 | ||||||
chr8:133211296
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0272 | 2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.70-1568C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211296 | ||||||
chr8:133211502
|
G | A | 1 | a0004c0019t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.70-1362G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211502 | ||||||
chr8:133211521
|
C | T | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(238): Show | 259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.70-1343C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211521 | ||||||
chr8:133211555
|
G | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0186 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.70-1309G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211555 | ||||||
chr8:133211712
|
C | T | 6 | a0001c0001t0005g0157a0001c0001t0008g0111a0001c0001t0008g0122others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-1152C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211712 | ||||||
chr8:133211724
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.70-1140G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211724 | ||||||
chr8:133211819
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.70-1045C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211819 | ||||||
chr8:133211835
|
C | G | 1 | a0001c0001t0008g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.70-1029C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211835 | ||||||
chr8:133211923
|
C | G | 24 | a0001c0001t0001g0112a0001c0001t0001g0156a0001c0001t0001g0221others(21): Show | 28 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.70-941C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133211923 | ||||||
chr8:133212104
|
G | A | 3 | a0001c0001t0005g0047a0001c0001t0005g0245a0004c0019t0001g0273 | 3 | HG01074.hp1 HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.70-760G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212104 | ||||||
chr8:133212128
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.70-736C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212128 | ||||||
chr8:133212182
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.70-682C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212182 | ||||||
chr8:133212205
|
A | C | 2 | a0004c0008t0029g0108a0004c0008t0037g0107 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.70-659A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212205 | ||||||
chr8:133212291
|
T | A | 25 | a0001c0001t0001g0112a0001c0001t0001g0156a0001c0001t0001g0221others(22): Show | 29 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.70-573T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212291 | ||||||
chr8:133212298
|
C | T | 2 | a0001c0001t0005g0047a0001c0001t0005g0245 | 2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.70-566C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212298 | ||||||
chr8:133212326
|
G | A | 119 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(116): Show | 129 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.70-538G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212326 | ||||||
chr8:133212335
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.70-529G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212335 | ||||||
chr8:133212359
|
G | A | 6 | a0001c0001t0005g0157a0001c0001t0008g0111a0001c0001t0008g0122others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-505G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212359 | ||||||
chr8:133212395
|
C | T | 1 | a0001c0002t0018g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70-469C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212395 | ||||||
chr8:133212474
|
C | T | 91 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(88): Show | 99 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.70-390C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212474 | ||||||
chr8:133212557
|
C | T | 3 | a0001c0001t0002g0278a0001c0001t0035g0246a0001c0010t0027g0275 | 3 | HG02258.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.70-307C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212557 | ||||||
chr8:133212621
|
C | A | 55 | a0001c0001t0001g0095a0001c0001t0001g0102a0001c0001t0001g0112others(52): Show | 59 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.70-243C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212621 | ||||||
chr8:133212635
|
A | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(140): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.70-229A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212635 | ||||||
chr8:133212681
|
T | G | 2 | a0001c0001t0005g0362a0001c0001t0022g0283 | 2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.70-183T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212681 | ||||||
chr8:133212687
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.70-177G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212687 | ||||||
chr8:133212692
|
A | G | 1 | a0001c0002t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.70-172A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212692 | ||||||
chr8:133212736
|
G | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.70-128G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212736 | ||||||
chr8:133212825
|
T | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(178): Show | 194 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.70-39T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212825 | ||||||
chr8:133212834
|
C | G | 1 | a0001c0002t0003g0040 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.70-30C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212834 | ||||||
chr8:133212856
|
C | T | 19 | a0001c0001t0001g0095a0001c0001t0001g0256a0001c0001t0001g0263others(16): Show | 19 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.70-8C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 1/4 | chr8 | 133212856 | ||||||
chr8:133213153
|
T | TC | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+12dupC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213153 | |||||
chr8:133213249
|
C | A | 3 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0002t0003g0193 | 3 | NA18986.hp2 NA18999.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.349+106C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213249 | ||||||
chr8:133213250
|
C | T | 9 | a0001c0003t0001g0153a0001c0003t0001g0274a0001c0003t0001g0277others(6): Show | 9 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+107C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213250 | ||||||
chr8:133213320
|
A | T | 5 | a0001c0001t0005g0249a0001c0001t0005g0362a0001c0001t0022g0283others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+177A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213320 | ||||||
chr8:133213368
|
C | T | 17 | a0001c0001t0001g0102a0001c0001t0005g0157a0001c0001t0006g0081others(14): Show | 17 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.349+225C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213368 | ||||||
chr8:133213409
|
G | C | 29 | a0001c0001t0001g0095a0001c0001t0001g0256a0001c0001t0001g0263others(26): Show | 29 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.349+266G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213409 | ||||||
chr8:133213415
|
C | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0371 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.349+272C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213415 | ||||||
chr8:133213566
|
C | G | 9 | a0001c0003t0001g0153a0001c0003t0001g0274a0001c0003t0001g0277others(6): Show | 9 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+423C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213566 | ||||||
chr8:133213621
|
C | G | 6 | a0001c0002t0004g0103a0001c0002t0004g0109a0001c0002t0012g0094others(3): Show | 6 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+478C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213621 | ||||||
chr8:133213636
|
T | A | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(239): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.349+493T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213636 | ||||||
chr8:133213644
|
T | G | 5 | a0001c0001t0005g0249a0001c0001t0005g0362a0001c0001t0022g0283others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+501T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213644 | ||||||
chr8:133213701
|
A | T | 1 | a0001c0001t0001g0365 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.349+558A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213701 | ||||||
chr8:133213749
|
T | C | 1 | a0001c0002t0018g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349+606T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213749 | ||||||
chr8:133213784
|
G | A | 7 | a0001c0001t0006g0081a0001c0001t0006g0143a0001c0001t0006g0235others(4): Show | 7 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+641G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213784 | ||||||
chr8:133213832
|
A | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+689A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213832 | ||||||
chr8:133213834
|
T | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+691T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213834 | ||||||
chr8:133213842
|
A | ATATACAC others(22): Show |
46 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(43): Show | 50 | HG00408.hp1 HG00558.hp2 HG01261.hp2 others(47): Show |
intron_variant | MODIFIER | c.349+751_349+779dup others(29): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213842 | |||||
chr8:133213865
|
A | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+722A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213865 | ||||||
chr8:133213867
|
T | C | 9 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+724T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213867 | ||||||
chr8:133213871
|
C | CACTATAT others(19): Show |
1 | a0001c0001t0001g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.349+728_349+729ins others(26): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213871 | ||||||
chr8:133213871
|
C | CTATA | 8 | a0001c0001t0001g0222a0001c0001t0016g0060a0002c0004t0004g0004others(5): Show | 9 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+729_349+732dup others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213871 | |||||
chr8:133213894
|
A | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+751A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213894 | ||||||
chr8:133213896
|
T | C | 8 | a0001c0001t0001g0222a0001c0001t0016g0060a0002c0004t0004g0004others(5): Show | 9 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+753T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213896 | ||||||
chr8:133213900
|
C | CACTATAT others(19): Show |
8 | a0001c0001t0001g0222a0001c0001t0016g0060a0002c0004t0004g0004others(5): Show | 9 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+757_349+758ins others(26): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213900 | ||||||
chr8:133213900
|
C | CTATA | 3 | a0001c0001t0001g0035a0001c0001t0002g0025a0001c0001t0002g0038 | 3 | HG02109.hp1 NA18969.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.349+758_349+761dup others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213900 | |||||
chr8:133213900
|
C | CTATACAC others(323): Show |
1 | a0001c0014t0001g0327 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.349+779_349+780ins others(330): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213900 | |||||
chr8:133213900
|
C | CTATACAC others(356): Show |
2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | NA18966.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.349+779_349+780ins others(363): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213900 | |||||
chr8:133213920
|
T | TTAAATAT others(165): Show |
1 | a0001c0001t0001g0335 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.349+779_349+780ins others(172): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213920 | |||||
chr8:133213920
|
T | TTAAATAT others(136): Show |
31 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0092others(28): Show | 34 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.349+779_349+780ins others(143): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213920 | |||||
chr8:133213923
|
T | A | 4 | a0001c0001t0005g0249a0001c0001t0024g0255a0001c0002t0004g0276others(1): Show | 4 | HG02965.hp2 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+780T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213923 | ||||||
chr8:133213929
|
C | CTATATAT others(108): Show |
1 | a0001c0001t0002g0189 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.349+814_349+815ins others(115): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | CTATATAT others(106): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0221a0001c0001t0019g0098 | 3 | HG02735.hp2 HG02970.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.349+814_349+815ins others(113): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | CTATATAT others(107): Show |
18 | a0001c0001t0001g0112a0001c0001t0002g0001a0001c0001t0002g0054others(15): Show | 22 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.349+814_349+815ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | CTATATAT others(107): Show |
41 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(38): Show | 45 | HG00408.hp1 HG00558.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.349+841_349+842ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | CTATATAT others(127): Show |
2 | a0001c0001t0001g0130a0001c0020t0001g0361 | 2 | NA18998.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.349+841_349+842ins others(134): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | CTATATAT others(109): Show |
6 | a0001c0001t0006g0081a0001c0001t0006g0143a0001c0001t0006g0235others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(116): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | CTATATAT others(107): Show |
1 | a0001c0002t0011g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | CTATATAT others(88): Show |
1 | a0001c0001t0002g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(95): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | CTATATAT others(74): Show |
1 | a0001c0001t0001g0178 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.349+808_349+809ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213929 | |||||
chr8:133213929
|
C | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0092others(29): Show | 35 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.349+786C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213929 | ||||||
chr8:133213951
|
A | T | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+808A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213951 | ||||||
chr8:133213952
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+809G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213952 | ||||||
chr8:133213953
|
T | TATATACT others(219): Show |
1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+810_349+811ins others(226): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213953 | ||||||
chr8:133213953
|
T | TTATATAT others(74): Show |
1 | a0001c0002t0018g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213953 | |||||
chr8:133213958
|
T | TATACTAT others(195): Show |
1 | a0001c0002t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(202): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213958 | |||||
chr8:133213958
|
T | TATACTAT others(107): Show |
2 | a0001c0001t0002g0025a0001c0001t0002g0038 | 2 | NA18969.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.349+840_349+841ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213958 | |||||
chr8:133213962
|
C | CTATATAT others(251): Show |
2 | a0001c0001t0005g0047a0001c0001t0005g0245 | 2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.349+880_349+881ins others(258): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(247): Show |
2 | a0001c0001t0005g0362a0001c0001t0022g0283 | 2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.349+873_349+874ins others(254): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(225): Show |
2 | a0001c0001t0001g0061a0001c0001t0001g0115 | 2 | HG00741.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.349+873_349+874ins others(232): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(217): Show |
1 | a0004c0019t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(224): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(76): Show |
7 | a0001c0001t0001g0213a0001c0001t0006g0254a0001c0002t0004g0109others(4): Show | 7 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(83): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(74): Show |
1 | a0001c0012t0001g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(74): Show |
2 | a0001c0001t0001g0102a0001c0012t0001g0364 | 2 | HG02922.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.349+840_349+841ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(191): Show |
1 | a0001c0001t0001g0372 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(198): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(109): Show |
8 | a0001c0003t0001g0153a0001c0003t0001g0274a0001c0003t0001g0277others(5): Show | 8 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(116): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(163): Show |
2 | a0001c0001t0001g0175a0001c0001t0001g0184 | 2 | HG04204.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.349+840_349+841ins others(170): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(192): Show |
51 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(48): Show | 56 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(199): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(221): Show |
1 | a0008c0013t0001g0373 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(228): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(194): Show |
2 | a0001c0001t0001g0071a0001c0002t0003g0251 | 2 | HG02897.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.349+840_349+841ins others(201): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(191): Show |
1 | a0001c0001t0001g0113 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(198): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(139): Show |
1 | a0001c0003t0005g0233 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(146): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(190): Show |
3 | a0001c0001t0001g0017a0001c0001t0001g0323a0001c0001t0001g0358 | 4 | NA18948.hp2 NA18968.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(197): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(74): Show |
6 | a0001c0001t0005g0157a0001c0001t0008g0111a0001c0001t0008g0122others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(81): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | CTATATAT others(79): Show |
1 | a0001c0002t0018g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(86): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213962 | |||||
chr8:133213962
|
C | G | 1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+819C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213962 | ||||||
chr8:133213965
|
T | TATATACA others(269): Show |
2 | a0004c0008t0029g0108a0004c0008t0037g0107 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.349+840_349+841ins others(276): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213965 | |||||
chr8:133213975
|
A | ATATATAG others(281): Show |
1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349+840_349+841ins others(288): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213975 | |||||
chr8:133213977
|
A | ATATAGTT others(188): Show |
1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.349+840_349+841ins others(195): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213977 | |||||
chr8:133213982
|
G | GTTATATA others(161): Show |
6 | a0001c0001t0001g0256a0001c0001t0001g0272a0001c0001t0001g0345others(3): Show | 6 | HG01243.hp2 HG01884.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+840_349+841ins others(168): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213982 | |||||
chr8:133213991
|
T | C | 25 | a0001c0001t0001g0112a0001c0001t0001g0156a0001c0001t0001g0221others(22): Show | 29 | HG00140.hp1 HG00733.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.349+848T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213991 | ||||||
chr8:133213991
|
T | TATACTAT others(142): Show |
1 | a0001c0001t0002g0024 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.349+860_349+861ins others(149): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(173): Show |
5 | a0001c0001t0001g0286a0001c0002t0003g0169a0001c0002t0003g0194others(2): Show | 5 | HG00741.hp1 HG01358.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+880_349+881ins others(180): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(136): Show |
1 | a0001c0001t0002g0068 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(143): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(107): Show |
14 | a0001c0001t0001g0028a0001c0001t0001g0219a0001c0001t0001g0300others(11): Show | 14 | HG00621.hp1 HG00639.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.349+873_349+874ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(140): Show |
98 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0090others(95): Show | 102 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.349+873_349+874ins others(147): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(173): Show |
6 | a0001c0001t0002g0338a0001c0002t0003g0033a0001c0002t0003g0048others(3): Show | 6 | HG00423.hp2 HG00735.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+873_349+874ins others(180): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(206): Show |
1 | a0001c0002t0003g0049 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(213): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(138): Show |
1 | a0001c0001t0001g0203 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.349+873_349+874ins others(145): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(130): Show |
1 | a0001c0001t0002g0349 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(137): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213991
|
T | TATACTAT others(107): Show |
1 | a0001c0015t0002g0295 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.349+873_349+874ins others(114): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213991 | |||||
chr8:133213998
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0256a0001c0001t0001g0272others(4): Show | 7 | HG01243.hp2 HG01884.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+855T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133213998 | ||||||
chr8:133213998
|
T | TATATACA others(163): Show |
2 | a0001c0001t0005g0096a0001c0001t0005g0097 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.349+873_349+874ins others(170): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213998 | |||||
chr8:133213998
|
T | TATATACA others(194): Show |
10 | a0001c0001t0001g0095a0001c0001t0001g0263a0001c0001t0001g0279others(7): Show | 10 | HG01109.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+873_349+874ins others(201): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133213998 | |||||
chr8:133214016
|
TAG | T | 5 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(2): Show | 5 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+874_349+875del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214016 | ||||||
chr8:133214024
|
C | T | 38 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0095others(35): Show | 39 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.349+881C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214024 | ||||||
chr8:133214037
|
C | A | 5 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(2): Show | 5 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+894C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214037 | ||||||
chr8:133214049
|
TAG | T | 4 | a0002c0004t0004g0004a0002c0004t0004g0046a0002c0004t0004g0080others(1): Show | 5 | HG02451.hp2 HG02486.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+907_349+908del others(2): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214049 | ||||||
chr8:133214057
|
C | T | 38 | a0001c0001t0001g0019a0001c0001t0001g0035a0001c0001t0001g0095others(35): Show | 39 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.349+914C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214057 | ||||||
chr8:133214063
|
A | ACTATATA others(285): Show |
5 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(2): Show | 5 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+920_349+921ins others(292): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214063 | ||||||
chr8:133214063
|
A | ATATATAA others(318): Show |
4 | a0002c0004t0004g0004a0002c0004t0004g0046a0002c0004t0004g0080others(1): Show | 5 | HG02451.hp2 HG02486.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+926_349+927ins others(325): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214063 | |||||
chr8:133214070
|
C | CACTATAT others(558): Show |
1 | a0001c0001t0001g0219 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.349+944_349+945ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(525): Show |
1 | a0001c0001t0001g0205 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(501): Show |
1 | a0001c0001t0002g0239 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(508): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(592): Show |
2 | a0001c0001t0001g0292a0001c0001t0002g0293 | 2 | NA18988.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(599): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(629): Show |
2 | a0001c0001t0001g0027a0001c0001t0002g0026 | 2 | NA18964.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(636): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(596): Show |
1 | a0001c0001t0001g0209 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(596): Show |
1 | a0001c0001t0001g0298 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(596): Show |
60 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(57): Show | 67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(629): Show |
1 | a0001c0001t0001g0336 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(636): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(568): Show |
1 | a0001c0002t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(575): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(558): Show |
1 | a0001c0002t0003g0127 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(558): Show |
8 | a0001c0001t0001g0129a0001c0002t0003g0032a0001c0002t0003g0077others(5): Show | 8 | HG01433.hp1 HG02698.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(558): Show |
2 | a0001c0001t0002g0304a0001c0001t0002g0342 | 2 | NA19009.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(596): Show |
2 | a0001c0001t0001g0174a0001c0001t0001g0186 | 2 | HG03669.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(565): Show |
1 | a0001c0001t0001g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(572): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(596): Show |
1 | a0001c0001t0001g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(524): Show |
1 | a0001c0001t0002g0018 | 2 | NA19002.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(531): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(563): Show |
2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02071.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.349+946_349+947ins others(570): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(525): Show |
44 | a0001c0001t0001g0044a0001c0001t0001g0085a0001c0001t0001g0203others(41): Show | 46 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(558): Show |
1 | a0001c0001t0002g0338 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(525): Show |
51 | a0001c0001t0001g0028a0001c0001t0001g0090a0001c0001t0001g0148others(48): Show | 52 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(558): Show |
1 | a0001c0001t0002g0315 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(525): Show |
2 | a0001c0001t0001g0303a0001c0001t0002g0201 | 2 | HG00621.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(525): Show |
1 | a0001c0001t0002g0149 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(491): Show |
1 | a0003c0006t0001g0045 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(498): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(523): Show |
1 | a0003c0007t0017g0124 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(530): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(492): Show |
11 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0007g0118others(8): Show | 11 | HG00639.hp2 HG01123.hp1 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(499): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(492): Show |
1 | a0001c0001t0002g0349 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(499): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(525): Show |
1 | a0001c0015t0002g0295 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(532): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(629): Show |
1 | a0001c0001t0001g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(636): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(601): Show |
1 | a0001c0002t0012g0363 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(608): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(601): Show |
4 | a0001c0002t0004g0109a0001c0002t0012g0094a0001c0002t0028g0236others(1): Show | 4 | HG02145.hp2 HG02486.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(608): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(596): Show |
1 | a0001c0001t0001g0268 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(603): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(602): Show |
2 | a0001c0001t0002g0278a0001c0010t0027g0275 | 2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.349+946_349+947ins others(609): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(569): Show |
1 | a0001c0001t0002g0241 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(576): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(600): Show |
2 | a0001c0001t0002g0054a0001c0002t0003g0243 | 2 | HG00733.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(607): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(569): Show |
16 | a0001c0001t0001g0112a0001c0001t0001g0156a0001c0001t0001g0221others(13): Show | 20 | HG00140.hp1 HG00733.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(576): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(568): Show |
1 | a0001c0001t0002g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(575): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(492): Show |
1 | a0001c0003t0015g0259 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.349+948_349+949ins others(499): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(501): Show |
4 | a0001c0003t0005g0233a0001c0003t0014g0076a0001c0003t0014g0346others(1): Show | 4 | HG03209.hp1 HG03540.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+948_349+949ins others(508): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(468): Show |
4 | a0001c0003t0001g0153a0001c0003t0001g0274a0001c0003t0001g0277others(1): Show | 4 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+948_349+949ins others(475): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(531): Show |
1 | a0004c0019t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(538): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(436): Show |
1 | a0001c0001t0001g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(443): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(427): Show |
14 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0061others(11): Show | 16 | HG00642.hp1 HG00741.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.349+948_349+949ins others(434): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(436): Show |
1 | a0001c0001t0001g0372 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(443): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(438): Show |
2 | a0001c0001t0005g0362a0001c0001t0022g0283 | 2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.349+948_349+949ins others(445): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(373): Show |
2 | a0001c0001t0001g0192a0001c0001t0002g0188 | 2 | HG01928.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.349+948_349+949ins others(380): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(427): Show |
1 | a0001c0001t0001g0344 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(434): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(436): Show |
41 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(38): Show | 45 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.349+948_349+949ins others(443): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(465): Show |
2 | a0001c0001t0001g0323a0001c0001t0001g0358 | 2 | NA18968.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.349+948_349+949ins others(472): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(438): Show |
2 | a0001c0001t0005g0047a0001c0001t0005g0245 | 2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.349+948_349+949ins others(445): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(427): Show |
1 | a0001c0005t0001g0183 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(434): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(434): Show |
1 | a0001c0001t0001g0218 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.349+948_349+949ins others(441): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(793): Show |
3 | a0001c0001t0005g0249a0001c0001t0024g0255a0001c0002t0004g0276 | 3 | HG02965.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.349+948_349+949ins others(800): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(512): Show |
2 | a0001c0001t0008g0100a0001c0001t0020g0042 | 2 | HG01106.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.349+940_349+941ins others(519): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(376): Show |
1 | a0001c0014t0001g0327 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.349+939_349+940ins others(383): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(315): Show |
1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.349+939_349+940ins others(322): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(369): Show |
12 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0272others(9): Show | 12 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.349+939_349+940ins others(376): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(338): Show |
6 | a0001c0001t0001g0095a0001c0001t0001g0279a0001c0001t0001g0371others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+939_349+940ins others(345): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | CACTATAT others(380): Show |
2 | a0004c0008t0029g0108a0004c0008t0037g0107 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.349+939_349+940ins others(387): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214070 | |||||
chr8:133214070
|
C | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0222a0001c0001t0016g0060others(6): Show | 10 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+927C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214070 | ||||||
chr8:133214072
|
C | CTATATAT others(535): Show |
6 | a0001c0001t0006g0081a0001c0001t0006g0143a0001c0001t0006g0235others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(542): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(635): Show |
1 | a0001c0002t0018g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(642): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(568): Show |
1 | a0001c0001t0006g0254 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(575): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(401): Show |
1 | a0001c0012t0001g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.349+946_349+947ins others(408): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(646): Show |
1 | a0001c0001t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(653): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(622): Show |
1 | a0001c0012t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(629): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(558): Show |
6 | a0001c0001t0005g0157a0001c0001t0008g0111a0001c0001t0008g0122others(3): Show | 6 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+946_349+947ins others(565): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(613): Show |
1 | a0001c0002t0011g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(620): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(613): Show |
1 | a0001c0002t0018g0232 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+946_349+947ins others(620): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214072
|
C | CTATATAT others(376): Show |
2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | NA18966.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.349+939_349+940ins others(383): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214072 | |||||
chr8:133214084
|
G | GTTATATA others(405): Show |
1 | a0001c0001t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.349+948_349+949ins others(412): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214084 | |||||
chr8:133214085
|
T | TTATACAT others(656): Show |
2 | a0001c0001t0001g0317a0001c0001t0001g0326 | 2 | NA18993.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(663): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214085 | |||||
chr8:133214085
|
T | TTATACAT others(494): Show |
2 | a0001c0001t0009g0078a0001c0001t0009g0079 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+946_349+947ins others(501): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214085 | |||||
chr8:133214092
|
A | T | 3 | a0001c0001t0001g0072a0001c0001t0009g0078a0001c0001t0009g0079 | 3 | HG00738.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+949A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214092 | ||||||
chr8:133214103
|
G | C | 18 | a0001c0001t0001g0072a0001c0001t0001g0256a0001c0001t0001g0263others(15): Show | 18 | HG00738.hp1 HG01106.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+960G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214103 | ||||||
chr8:133214110
|
T | TAGTAGTT others(20): Show |
5 | a0001c0001t0001g0130a0001c0001t0001g0353a0001c0001t0001g0354others(2): Show | 5 | HG01515.hp1 HG02738.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+993_349+1019du others(28): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214110 | |||||
chr8:133214122
|
AT | A | 3 | a0001c0001t0001g0072a0001c0001t0009g0078a0001c0001t0009g0079 | 3 | HG00738.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+980delT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214122 | ||||||
chr8:133214124
|
AACT | A | 9 | a0001c0003t0001g0153a0001c0003t0001g0274a0001c0003t0001g0277others(6): Show | 9 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.349+986_349+988del others(3): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214124 | |||||
chr8:133214128
|
AC | A | 3 | a0001c0001t0001g0072a0001c0001t0009g0078a0001c0001t0009g0079 | 3 | HG00738.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+986delC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214128 | ||||||
chr8:133214137
|
C | T | 2 | a0001c0001t0009g0078a0001c0001t0009g0079 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.349+994C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214137 | ||||||
chr8:133214156
|
CTA | C | 37 | a0001c0001t0001g0095a0001c0001t0001g0256a0001c0001t0001g0263others(34): Show | 37 | HG01106.hp1 HG01109.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.349+1024_349+1025d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214156 | |||||
chr8:133214277
|
TA | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1136delA | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214277 | |||||
chr8:133214290
|
TA | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1149delA | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214290 | |||||
chr8:133214300
|
C | T | 1 | a0001c0001t0038g0208 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.349+1157C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214300 | ||||||
chr8:133214346
|
C | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1203C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214346 | ||||||
chr8:133214362
|
C | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1219C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214362 | ||||||
chr8:133214364
|
G | C | 6 | a0001c0002t0004g0103a0001c0002t0004g0109a0001c0002t0012g0094others(3): Show | 6 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+1221G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214364 | ||||||
chr8:133214364
|
G | T | 367 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(364): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.349+1221G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214364 | ||||||
chr8:133214395
|
G | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1252G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214395 | ||||||
chr8:133214397
|
A | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1254A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214397 | ||||||
chr8:133214401
|
G | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1258G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214401 | ||||||
chr8:133214411
|
C | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1268C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214411 | ||||||
chr8:133214426
|
C | CT | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.349+1287dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214426 | |||||
chr8:133214471
|
T | A | 1 | a0001c0001t0002g0342 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.349+1328T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214471 | ||||||
chr8:133214474
|
T | A | 1 | a0001c0002t0003g0152 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.349+1331T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214474 | ||||||
chr8:133214507
|
G | GGTT | 4 | a0001c0001t0001g0322a0001c0001t0001g0334a0001c0001t0002g0278others(1): Show | 4 | HG02055.hp1 HG03471.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1386_349+1388d others(5): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214507 | |||||
chr8:133214507
|
G | GGTTGTTG others(2): Show |
6 | a0001c0001t0001g0095a0001c0001t0001g0279a0001c0001t0001g0371others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.349+1380_349+1388d others(11): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214507 | |||||
chr8:133214507
|
G | GGTTGTTG others(5): Show |
14 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0272others(11): Show | 14 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.349+1377_349+1388d others(14): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133214507 | |||||
chr8:133214510
|
T | G | 1 | a0001c0001t0002g0285 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.349+1367T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214510 | ||||||
chr8:133214569
|
G | A | 1 | a0001c0001t0007g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.349+1426G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214569 | ||||||
chr8:133214636
|
C | T | 90 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(87): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.349+1493C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214636 | ||||||
chr8:133214740
|
A | C | 1 | a0001c0002t0003g0056 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.349+1597A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214740 | ||||||
chr8:133214832
|
G | A | 2 | a0004c0008t0029g0108a0004c0008t0037g0107 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.349+1689G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214832 | ||||||
chr8:133214954
|
A | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(94): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.349+1811A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214954 | ||||||
chr8:133214982
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.349+1839C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133214982 | ||||||
chr8:133215076
|
T | C | 2 | a0001c0002t0011g0250a0001c0002t0018g0232 | 2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.349+1933T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215076 | ||||||
chr8:133215197
|
C | A | 1 | a0001c0001t0001g0284 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.349+2054C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215197 | ||||||
chr8:133215253
|
C | T | 60 | a0001c0001t0001g0028a0001c0001t0001g0090a0001c0001t0001g0148others(57): Show | 62 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.349+2110C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215253 | ||||||
chr8:133215457
|
T | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(131): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.349+2314T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215457 | ||||||
chr8:133215545
|
T | A | 18 | a0001c0001t0001g0095a0001c0001t0001g0256a0001c0001t0001g0263others(15): Show | 18 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.349+2402T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215545 | ||||||
chr8:133215733
|
A | G | 2 | a0001c0001t0005g0096a0001c0001t0005g0097 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.349+2590A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215733 | ||||||
chr8:133215736
|
C | A | 13 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0272others(10): Show | 13 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.349+2593C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215736 | ||||||
chr8:133215761
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.349+2618G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215761 | ||||||
chr8:133215775
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(106): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.349+2632G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215775 | ||||||
chr8:133215917
|
T | C | 1 | a0001c0002t0004g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.349+2774T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215917 | ||||||
chr8:133215953
|
A | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(64): Show | 73 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.349+2810A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215953 | ||||||
chr8:133215965
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(112): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.349+2822C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133215965 | ||||||
chr8:133215984
|
T | TAC | 21 | a0001c0001t0001g0102a0001c0001t0001g0331a0001c0001t0001g0332others(18): Show | 21 | HG00609.hp2 HG01167.hp2 HG02129.hp1 others(18): Show |
intron_variant | MODIFIER | c.349+2863_349+2864d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133215984 | |||||
chr8:133215984
|
TAC | T | 47 | a0001c0001t0001g0095a0001c0001t0001g0112a0001c0001t0001g0156others(44): Show | 51 | HG00140.hp1 HG00323.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.349+2863_349+2864d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133215984 | |||||
chr8:133216042
|
A | T | 1 | a0004c0019t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.349+2899A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216042 | ||||||
chr8:133216054
|
A | G | 115 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(112): Show | 125 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.349+2911A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216054 | ||||||
chr8:133216279
|
T | C | 11 | a0001c0001t0002g0001a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 15 | HG00733.hp2 HG01074.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.349+3136T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216279 | ||||||
chr8:133216563
|
AC | A | 8 | a0001c0001t0006g0081a0001c0001t0006g0143a0001c0001t0006g0235others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+3422delC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133216563 | |||||
chr8:133216627
|
G | A | 2 | a0004c0008t0029g0108a0004c0008t0037g0107 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.349+3484G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216627 | ||||||
chr8:133216663
|
A | C | 5 | a0001c0001t0005g0249a0001c0001t0005g0362a0001c0001t0022g0283others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+3520A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216663 | ||||||
chr8:133216687
|
T | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(190): Show | 206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.349+3544T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216687 | ||||||
chr8:133216739
|
T | C | 8 | a0001c0001t0006g0081a0001c0001t0006g0143a0001c0001t0006g0235others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+3596T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216739 | ||||||
chr8:133216756
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.349+3613G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216756 | ||||||
chr8:133216786
|
A | C | 1 | a0001c0001t0002g0054 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.349+3643A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216786 | ||||||
chr8:133216875
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.350-3706C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216875 | ||||||
chr8:133216909
|
C | G | 12 | a0001c0001t0001g0035a0001c0001t0001g0095a0001c0001t0001g0222others(9): Show | 13 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.350-3672C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133216909 | ||||||
chr8:133217060
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.350-3521C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217060 | ||||||
chr8:133217102
|
T | C | 4 | a0001c0001t0002g0239a0004c0008t0029g0108a0004c0008t0037g0107others(1): Show | 4 | HG02572.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-3479T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217102 | ||||||
chr8:133217198
|
G | T | 1 | a0001c0001t0001g0174 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.350-3383G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217198 | ||||||
chr8:133217265
|
C | A | 72 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(69): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.350-3316C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217265 | ||||||
chr8:133217292
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(191): Show | 207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.350-3289A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217292 | ||||||
chr8:133217547
|
G | A | 2 | a0001c0001t0005g0362a0001c0001t0022g0283 | 2 | HG01891.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.350-3034G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217547 | ||||||
chr8:133217640
|
C | A | 189 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(186): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.350-2941C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217640 | ||||||
chr8:133217643
|
G | A | 2 | a0001c0001t0020g0042a0004c0008t0029g0108 | 2 | HG01106.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.350-2938G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217643 | ||||||
chr8:133217813
|
G | T | 1 | a0001c0002t0004g0103 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.350-2768G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217813 | ||||||
chr8:133217860
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.350-2721G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133217860 | ||||||
chr8:133217936
|
C | CCACA | 4 | a0001c0001t0005g0249a0001c0001t0006g0264a0001c0001t0024g0255others(1): Show | 4 | HG02965.hp2 HG02976.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-2623_350-2620d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(5): Show |
2 | a0001c0001t0002g0239a0001c0012t0001g0067 | 2 | HG02717.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.350-2631_350-2620d others(14): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(7): Show |
12 | a0001c0001t0005g0157a0001c0001t0008g0111a0001c0001t0008g0122others(9): Show | 12 | HG01167.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.350-2633_350-2620d others(16): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(9): Show |
7 | a0001c0001t0001g0086a0001c0001t0001g0210a0001c0001t0001g0263others(4): Show | 7 | HG01074.hp1 HG02055.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-2635_350-2620d others(18): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(11): Show |
29 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0105others(26): Show | 29 | HG00140.hp2 HG00642.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.350-2637_350-2620d others(20): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(13): Show |
79 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0014others(76): Show | 86 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.350-2639_350-2620d others(22): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(15): Show |
80 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0022others(77): Show | 87 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.350-2641_350-2620d others(24): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(17): Show |
23 | a0001c0001t0001g0028a0001c0001t0001g0090a0001c0001t0001g0131others(20): Show | 23 | HG00597.hp1 HG01891.hp2 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.350-2643_350-2620d others(26): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(19): Show |
1 | a0001c0001t0001g0228 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.350-2620_350-2619i others(28): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(23): Show |
1 | a0001c0001t0001g0035 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.350-2620_350-2619i others(32): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(13): Show |
2 | a0001c0001t0001g0257a0001c0001t0002g0188 | 2 | HG01928.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.350-2632_350-2631i others(22): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(15): Show |
63 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(60): Show | 69 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.350-2632_350-2631i others(24): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(17): Show |
4 | a0001c0001t0001g0036a0001c0001t0001g0101a0001c0001t0001g0116others(1): Show | 4 | HG00642.hp1 HG01934.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-2632_350-2631i others(26): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133217936
|
C | CCACACAC others(19): Show |
2 | a0001c0001t0001g0061a0001c0001t0001g0115 | 2 | HG00741.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.350-2632_350-2631i others(28): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133217936 | |||||
chr8:133218074
|
C | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(145): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.350-2507C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218074 | ||||||
chr8:133218212
|
G | C | 1 | a0001c0001t0002g0307 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.350-2369G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218212 | ||||||
chr8:133218225
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0038g0208 | 2 | NA19010.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.350-2356C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218225 | ||||||
chr8:133218401
|
C | T | 68 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(65): Show | 74 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.350-2180C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218401 | ||||||
chr8:133218539
|
C | A | 80 | a0001c0001t0001g0028a0001c0001t0001g0090a0001c0001t0001g0148others(77): Show | 86 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.350-2042C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218539 | ||||||
chr8:133218548
|
A | G | 1 | a0001c0001t0007g0118 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.350-2033A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218548 | ||||||
chr8:133218568
|
G | A | 1 | a0001c0001t0001g0316 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.350-2013G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218568 | ||||||
chr8:133218576
|
T | A | 1 | a0001c0001t0002g0104 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.350-2005T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218576 | ||||||
chr8:133218773
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.350-1808T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218773 | ||||||
chr8:133218996
|
TC | T | 3 | a0001c0001t0007g0158a0001c0001t0007g0258a0001c0001t0007g0347 | 3 | HG02280.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.350-1584delC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133218996 | ||||||
chr8:133219009
|
C | T | 1 | a0001c0001t0008g0100 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.350-1572C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219009 | ||||||
chr8:133219025
|
T | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0178others(5): Show | 10 | HG00408.hp1 NA18973.hp2 NA18978.hp2 others(7): Show |
intron_variant | MODIFIER | c.350-1556T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219025 | ||||||
chr8:133219069
|
C | T | 6 | a0001c0002t0004g0103a0001c0002t0004g0109a0001c0002t0012g0094others(3): Show | 6 | HG01167.hp2 HG02145.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1512C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219069 | ||||||
chr8:133219353
|
T | A | 1 | a0001c0002t0028g0236 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.350-1228T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219353 | ||||||
chr8:133219425
|
C | T | 1 | a0004c0019t0001g0273 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.350-1156C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219425 | ||||||
chr8:133219564
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0013others(73): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.350-1017C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219564 | ||||||
chr8:133219589
|
C | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(88): Show | 98 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.350-992C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219589 | ||||||
chr8:133219620
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.350-961T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219620 | ||||||
chr8:133219691
|
G | A | 7 | a0001c0002t0004g0103a0001c0002t0004g0109a0001c0002t0012g0094others(4): Show | 7 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-890G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219691 | ||||||
chr8:133219791
|
G | C | 2 | a0001c0001t0002g0312a0001c0002t0003g0052 | 2 | HG02132.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.350-790G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219791 | ||||||
chr8:133219969
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.350-612G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133219969 | ||||||
chr8:133220060
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(83): Show | 93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.350-521T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220060 | ||||||
chr8:133220164
|
G | T | 1 | a0003c0007t0017g0242 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.350-417G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220164 | ||||||
chr8:133220181
|
C | T | 1 | a0001c0002t0010g0262 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.350-400C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220181 | ||||||
chr8:133220194
|
C | CT | 86 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(83): Show | 93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.350-378dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 133220194 | |||||
chr8:133220212
|
G | A | 1 | a0001c0002t0003g0253 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.350-369G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220212 | ||||||
chr8:133220315
|
G | A | 1 | a0001c0001t0001g0317 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.350-266G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220315 | ||||||
chr8:133220375
|
C | T | 3 | a0004c0008t0029g0108a0004c0008t0037g0107a0004c0019t0001g0273 | 3 | HG02572.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.350-206C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220375 | ||||||
chr8:133220533
|
C | T | 1 | a0001c0001t0001g0017 | 2 | NA18948.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.350-48C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 2/4 | chr8 | 133220533 | ||||||
chr8:133220967
|
G | T | 2 | a0001c0001t0002g0217a0001c0001t0002g0337 | 2 | HG00621.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.610+126G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133220967 | ||||||
chr8:133220982
|
C | T | 6 | a0001c0001t0005g0157a0001c0001t0008g0111a0001c0001t0008g0122others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.610+141C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133220982 | ||||||
chr8:133221159
|
G | A | 3 | a0004c0008t0029g0108a0004c0008t0037g0107a0004c0019t0001g0273 | 3 | HG02572.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.610+318G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221159 | ||||||
chr8:133221187
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.610+346C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221187 | ||||||
chr8:133221532
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.610+691C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221532 | ||||||
chr8:133221661
|
G | T | 12 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0272others(9): Show | 12 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.610+820G>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221661 | ||||||
chr8:133221724
|
A | AATGGATG others(1): Show |
103 | a0001c0001t0001g0028a0001c0001t0001g0090a0001c0001t0001g0095others(100): Show | 109 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.610+894_610+901dup others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133221724 | |||||
chr8:133221852
|
G | A | 1 | a0001c0002t0028g0236 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.610+1011G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221852 | ||||||
chr8:133221908
|
T | C | 83 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(80): Show | 90 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.610+1067T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133221908 | ||||||
chr8:133221919
|
A | AGGAT | 3 | a0001c0001t0001g0023a0001c0001t0001g0355a0001c0002t0018g0041 | 3 | HG03195.hp2 NA18991.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.610+1099_610+1102d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133221919 | |||||
chr8:133221919
|
AGGAT | A | 7 | a0001c0001t0005g0249a0001c0001t0005g0362a0001c0001t0022g0283others(4): Show | 7 | HG01891.hp2 HG02572.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+1099_610+1102d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133221919 | |||||
chr8:133222083
|
C | T | 8 | a0001c0001t0006g0081a0001c0001t0006g0143a0001c0001t0006g0235others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.610+1242C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222083 | ||||||
chr8:133222095
|
T | C | 1 | a0001c0005t0001g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.610+1254T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222095 | ||||||
chr8:133222115
|
TAATG | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0230a0001c0001t0001g0306 | 3 | NA18950.hp2 NA18977.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.610+1275_610+1278d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222115 | ||||||
chr8:133222507
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0279a0001c0001t0001g0371 | 3 | HG02723.hp2 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.610+1666T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222507 | ||||||
chr8:133222585
|
A | G | 7 | a0001c0002t0004g0103a0001c0002t0004g0109a0001c0002t0012g0094others(4): Show | 7 | HG01167.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+1744A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222585 | ||||||
chr8:133222679
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.610+1838G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222679 | ||||||
chr8:133222737
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.610+1896G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222737 | ||||||
chr8:133222807
|
T | TA | 17 | a0001c0001t0001g0035a0001c0001t0002g0025a0001c0003t0001g0274others(14): Show | 17 | HG00642.hp2 HG01070.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.610+1974dupA | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133222807 | |||||
chr8:133222808
|
A | T | 11 | a0001c0001t0005g0096a0001c0001t0005g0097a0001c0001t0026g0234others(8): Show | 11 | HG01109.hp2 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.610+1967A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133222808 | ||||||
chr8:133223014
|
C | T | 1 | a0001c0002t0003g0200 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.610+2173C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223014 | ||||||
chr8:133223112
|
T | C | 10 | a0001c0002t0018g0041a0001c0002t0018g0232a0003c0006t0001g0030others(7): Show | 10 | HG00642.hp2 HG01070.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.610+2271T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223112 | ||||||
chr8:133223132
|
A | G | 1 | a0001c0001t0002g0293 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.611-2258A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223132 | ||||||
chr8:133223133
|
G | C | 1 | a0001c0001t0002g0293 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.611-2257G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223133 | ||||||
chr8:133223150
|
C | T | 1 | a0001c0001t0035g0246 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.611-2240C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223150 | ||||||
chr8:133223157
|
C | A | 14 | a0001c0003t0001g0153a0001c0003t0001g0274a0001c0003t0001g0277others(11): Show | 14 | HG00642.hp2 HG01168.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.611-2233C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223157 | ||||||
chr8:133223212
|
G | A | 1 | a0001c0001t0002g0307 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.611-2178G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223212 | ||||||
chr8:133223228
|
A | G | 7 | a0001c0002t0004g0109a0003c0006t0001g0030a0003c0006t0001g0045others(4): Show | 7 | HG00642.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.611-2162A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223228 | ||||||
chr8:133223430
|
T | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0186 | 2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.611-1960T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223430 | ||||||
chr8:133223573
|
T | C | 234 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(231): Show | 245 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.611-1817T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223573 | ||||||
chr8:133223575
|
C | T | 1 | a0001c0001t0020g0042 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.611-1815C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223575 | ||||||
chr8:133223641
|
T | A | 3 | a0001c0001t0001g0331a0001c0010t0027g0275a0001c0010t0031g0366 | 3 | HG02055.hp2 HG02965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.611-1749T>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223641 | ||||||
chr8:133223641
|
T | TCA | 116 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0009others(113): Show | 125 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.611-1737_611-1736d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133223641 | |||||
chr8:133223654
|
C | T | 1 | a0001c0002t0003g0077 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.611-1736C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223654 | ||||||
chr8:133223707
|
A | G | 5 | a0001c0002t0012g0094a0001c0002t0012g0106a0001c0002t0012g0363others(2): Show | 5 | HG01167.hp2 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-1683A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223707 | ||||||
chr8:133223764
|
G | A | 1 | a0001c0001t0001g0344 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.611-1626G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223764 | ||||||
chr8:133223805
|
C | T | 1 | a0001c0002t0004g0082 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.611-1585C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223805 | ||||||
chr8:133223814
|
T | C | 1 | a0001c0001t0005g0096 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.611-1576T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223814 | ||||||
chr8:133223856
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0205 | 3 | HG03017.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.611-1534T>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223856 | ||||||
chr8:133223987
|
C | G | 5 | a0001c0002t0012g0094a0001c0002t0012g0106a0001c0002t0012g0363others(2): Show | 5 | HG01167.hp2 HG02622.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.611-1403C>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133223987 | ||||||
chr8:133224044
|
GC | G | 220 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(217): Show | 233 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.611-1345delC | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224044 | ||||||
chr8:133224211
|
A | C | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.611-1179A>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224211 | ||||||
chr8:133224213
|
T | C | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.611-1177T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224213 | ||||||
chr8:133224221
|
C | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.611-1169C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224221 | ||||||
chr8:133224225
|
A | T | 373 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(370): Show | 395 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(392): Show |
intron_variant | MODIFIER | c.611-1165A>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224225 | ||||||
chr8:133224229
|
C | CT | 14 | a0001c0001t0002g0005a0001c0001t0002g0029a0001c0001t0002g0053others(11): Show | 15 | HG00621.hp2 HG00639.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.611-1132dupT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | |||||
chr8:133224229
|
C | CTT | 8 | a0001c0001t0002g0001a0001c0001t0002g0068a0001c0001t0002g0154others(5): Show | 11 | HG01074.hp2 HG01258.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.611-1133_611-1132d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | |||||
chr8:133224229
|
CT | C | 25 | a0001c0001t0001g0031a0001c0001t0002g0201a0001c0001t0005g0097others(22): Show | 25 | HG00735.hp2 HG01106.hp2 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.611-1132delT | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | |||||
chr8:133224229
|
CTT | C | 67 | a0001c0001t0001g0055a0001c0001t0001g0092a0001c0001t0001g0160others(64): Show | 70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.611-1133_611-1132d others(4): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | |||||
chr8:133224229
|
CTTT | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0012others(102): Show | 112 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.611-1134_611-1132d others(5): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | |||||
chr8:133224229
|
CTTTT | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(75): Show | 82 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.611-1135_611-1132d others(6): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | |||||
chr8:133224229
|
CTTTTT | C | 7 | a0001c0001t0001g0063a0001c0001t0001g0353a0001c0001t0005g0249others(4): Show | 7 | HG01169.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.611-1136_611-1132d others(7): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | |||||
chr8:133224229
|
CTTTTTT | C | 18 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0062others(15): Show | 20 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.611-1137_611-1132d others(8): Show |
CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224229 | |||||
chr8:133224493
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(199): Show | 215 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.611-897G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224493 | ||||||
chr8:133224532
|
C | T | 1 | a0001c0001t0001g0268 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.611-858C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224532 | ||||||
chr8:133224536
|
C | A | 2 | a0001c0001t0005g0047a0001c0001t0005g0245 | 2 | HG01074.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.611-854C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224536 | ||||||
chr8:133224650
|
C | T | 219 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(216): Show | 232 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.611-740C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224650 | ||||||
chr8:133224660
|
C | T | 2 | a0001c0003t0014g0076a0001c0003t0014g0346 | 2 | HG03209.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.611-730C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224660 | ||||||
chr8:133224674
|
C | A | 4 | a0001c0001t0008g0100a0001c0001t0008g0111a0001c0001t0008g0122others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-716C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224674 | ||||||
chr8:133224682
|
C | T | 2 | a0004c0008t0029g0108a0004c0008t0037g0107 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.611-708C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224682 | ||||||
chr8:133224703
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.611-687G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224703 | ||||||
chr8:133224705
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0140a0001c0005t0001g0136 | 3 | HG00558.hp2 NA18964.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.611-685C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224705 | ||||||
chr8:133224753
|
G | A | 4 | a0001c0001t0008g0100a0001c0001t0008g0111a0001c0001t0008g0122others(1): Show | 4 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.611-637G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224753 | ||||||
chr8:133224849
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(218): Show | 234 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.611-541A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133224849 | ||||||
chr8:133224935
|
CA | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(200): Show | 216 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.611-439delA | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 133224935 | |||||
chr8:133225029
|
G | A | 1 | a0001c0005t0001g0181 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.611-361G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133225029 | ||||||
chr8:133225335
|
G | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 235 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.611-55G>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133225335 | ||||||
chr8:133225378
|
C | A | 1 | a0001c0002t0004g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.611-12C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 3/4 | chr8 | 133225378 | ||||||
chr8:133225673
|
T | C | 2 | a0001c0002t0018g0041a0001c0002t0018g0232 | 2 | HG02257.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.804+90T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133225673 | ||||||
chr8:133225931
|
C | T | 1 | a0001c0002t0011g0250 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.804+348C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133225931 | ||||||
chr8:133226009
|
C | A | 3 | a0001c0002t0003g0193a0001c0002t0003g0206a0001c0002t0003g0207 | 3 | NA18947.hp1 NA18995.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.804+426C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226009 | ||||||
chr8:133226150
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.804+567G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226150 | ||||||
chr8:133226451
|
T | C | 2 | a0004c0008t0029g0108a0004c0008t0037g0107 | 2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.804+868T>C | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226451 | ||||||
chr8:133226528
|
G | A | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(278): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.805-883G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226528 | ||||||
chr8:133226573
|
C | T | 1 | a0001c0001t0002g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.805-838C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226573 | ||||||
chr8:133226778
|
A | G | 22 | a0001c0002t0010g0261a0001c0002t0010g0262a0001c0002t0010g0269others(19): Show | 22 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.805-633A>G | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226778 | ||||||
chr8:133226916
|
G | A | 51 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(48): Show | 55 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.805-495G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226916 | ||||||
chr8:133226934
|
C | A | 8 | a0001c0002t0012g0094a0001c0002t0012g0106a0001c0002t0012g0363others(5): Show | 8 | HG01167.hp2 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.805-477C>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226934 | ||||||
chr8:133226977
|
G | A | 18 | a0001c0002t0010g0261a0001c0002t0010g0262a0001c0002t0010g0269others(15): Show | 18 | HG01109.hp2 HG01167.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.805-434G>A | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133226977 | ||||||
chr8:133227035
|
C | T | 5 | a0001c0002t0003g0040a0001c0002t0003g0121a0001c0002t0003g0161others(2): Show | 5 | NA18957.hp1 NA18982.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.805-376C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133227035 | ||||||
chr8:133227049
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.805-362C>T | CCN4 | ENSG00000104415.14 | transcript | ENST00000250160.11 | protein_coding | 4/4 | chr8 | 133227049 |