geneid | 1105 |
---|---|
ensemblid | ENSG00000153922.12 |
hgncid | 1915 |
symbol | CHD1 |
name | chromodomain helicase DNA binding protein 1 |
refseq_nuc | NM_001270.4 |
refseq_prot | NP_001261.2 |
ensembl_nuc | ENST00000614616.5 |
ensembl_prot | ENSP00000483667.1 |
mane_status | MANE Select |
chr | chr5 |
start | 98853985 |
end | 98929007 |
strand | - |
ver | v1.2 |
region | chr5:98853985-98929007 |
region5000 | chr5:98848985-98934007 |
regionname0 | CHD1_chr5_98853985_98929007 |
regionname5000 | CHD1_chr5_98848985_98934007 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1710 | 260 | 60 | 43 | 119 | 7 | 29 | 92 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002 | 0/0 | 1709 | 71 | 28 | 18 | 20 | 2 | 3 | 19 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0003 | 0/0 | 1709 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0004 | 0/0 | 1710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0005 | 0/0 | 1710 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 5133 | 215 | 24 | 40 | 117 | 6 | 26 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0002 | 0/0 | 5130 | 71 | 28 | 18 | 20 | 2 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0003 | 0/0 | 5133 | 35 | 29 | 2 | 0 | 1 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0004 | 0/0 | 5133 | 6 | 6 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0005 | 0/0 | 5133 | 2 | 1 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0006 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0007 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0008 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0009 | 0/0 | 5130 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
c0010 | 0/0 | 5133 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3013 | 179 | 30 | 36 | 90 | 3 | 18 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0002 | 0/0 | 3023 | 58 | 26 | 17 | 12 | 1 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0003 | 0/0 | 3013 | 18 | 0 | 3 | 9 | 3 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0004 | 0/0 | 3013 | 13 | 0 | 0 | 11 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0005 | 0/0 | 3020 | 10 | 10 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0006 | 0/0 | 3023 | 9 | 8 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0007 | 0/0 | 3020 | 4 | 0 | 0 | 3 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0008 | 0/0 | 3013 | 4 | 0 | 0 | 4 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0009 | 0/0 | 3018 | 4 | 0 | 0 | 0 | 1 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0010 | 0/0 | 3023 | 4 | 0 | 0 | 4 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0011 | 0/0 | 3023 | 3 | 0 | 1 | 0 | 2 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0012 | 0/0 | 3023 | 3 | 3 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0013 | 0/0 | 3023 | 3 | 3 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0014 | 0/0 | 3013 | 3 | 0 | 0 | 3 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0015 | 0/0 | 3013 | 2 | 0 | 0 | 0 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0016 | 0/0 | 3023 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0017 | 0/0 | 3023 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0018 | 0/0 | 3020 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0019 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0020 | 0/0 | 3023 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0021 | 0/0 | 3013 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0022 | 0/0 | 3013 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0023 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0024 | 0/0 | 3023 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0025 | 0/0 | 3023 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0026 | 0/0 | 3013 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0027 | 0/0 | 3013 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0028 | 0/0 | 3023 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0029 | 0/0 | 3013 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
t0030 | 0/0 | 3013 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5133 | 215 | 24 | 40 | 117 | 6 | 26 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003 | 0/0 | 5133 | 35 | 29 | 2 | 0 | 1 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0004 | 0/0 | 5133 | 6 | 6 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0005 | 0/0 | 5133 | 2 | 1 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0006 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0008 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002 | 0/0 | 5130 | 71 | 28 | 18 | 20 | 2 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0003c0009 | 0/0 | 5130 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0004c0007 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0005c0010 | 0/0 | 5133 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 8145 | 168 | 23 | 35 | 87 | 3 | 18 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0003 | 0/0 | 8145 | 18 | 0 | 3 | 9 | 3 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0004 | 0/0 | 8145 | 13 | 0 | 0 | 11 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0008 | 0/0 | 8145 | 4 | 0 | 0 | 4 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0014 | 0/0 | 8145 | 3 | 0 | 0 | 3 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0015 | 0/0 | 8145 | 2 | 0 | 0 | 0 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0019 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0021 | 0/0 | 8145 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0023 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0026 | 0/0 | 8145 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0027 | 0/0 | 8145 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0029 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0001t0030 | 0/0 | 8145 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003t0002 | 0/0 | 8155 | 13 | 12 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003t0005 | 0/0 | 8152 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003t0006 | 0/0 | 8155 | 9 | 8 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003t0009 | 0/0 | 8150 | 4 | 0 | 0 | 0 | 1 | 3 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003t0012 | 0/0 | 8155 | 3 | 3 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003t0013 | 0/0 | 8155 | 3 | 3 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003t0020 | 0/0 | 8155 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0003t0028 | 0/0 | 8155 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0004t0001 | 0/0 | 8145 | 6 | 6 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0005t0001 | 0/0 | 8145 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0005t0022 | 0/0 | 8145 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0006t0001 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0001c0008t0001 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0002 | 0/0 | 8152 | 44 | 14 | 16 | 12 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0005 | 0/0 | 8149 | 9 | 9 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0007 | 0/0 | 8149 | 4 | 0 | 0 | 3 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0010 | 0/0 | 8152 | 4 | 0 | 0 | 4 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0011 | 0/0 | 8152 | 3 | 0 | 1 | 0 | 2 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0016 | 0/0 | 8152 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0017 | 0/0 | 8152 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0018 | 0/0 | 8149 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0024 | 0/0 | 8152 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0002c0002t0025 | 0/0 | 8152 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0003c0009t0002 | 0/0 | 8152 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0004c0007t0001 | 0/0 | 8145 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
a0005c0010t0001 | 0/0 | 8145 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | copy fasta | chr5 | 98848985 | 98934007 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0014g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0014g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0014g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0015g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0019g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0021g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0023g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0026g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0027g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0029g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0001t0030g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0005g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0009g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0009g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0009g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0009g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0012g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0012g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0012g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0013g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0013g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0020g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0003t0028g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0005t0022g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0006t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0001c0008t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0007g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0007g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0010g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0010g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0011g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0011g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0011g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0016g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0016g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0017g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0017g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0018g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0024g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0002c0002t0025g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0003c0009t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0004c0007t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
a0005c0010t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0002 | c0002 | t0011 | g0073 | EUR | FIN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00323 | hp2 | a0001 | c0003 | t0009 | g0191 | EUR | FIN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00408 | hp1 | a0001 | c0001 | t0019 | g0013 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | CHS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0109 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0227 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0116 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0110 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0108 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0117 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01081 | hp1 | a0005 | c0010 | t0001 | g0251 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0113 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01109 | hp1 | a0001 | c0003 | t0006 | g0063 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0120 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0126 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0125 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0195 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01255 | hp1 | a0001 | c0005 | t0022 | g0043 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01358 | hp1 | a0002 | c0002 | t0011 | g0075 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01433 | hp1 | a0001 | c0001 | t0027 | g0137 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0115 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01496 | hp2 | a0002 | c0002 | t0025 | g0133 | AMR | CLM | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01515 | hp1 | a0002 | c0002 | t0011 | g0076 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0305 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0307 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0306 | EUR | IBS | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01884 | hp2 | a0001 | c0003 | t0006 | g0066 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01891 | hp2 | a0001 | c0003 | t0002 | g0056 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0311 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01981 | hp1 | a0001 | c0001 | t0021 | g0162 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0310 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0321 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02055 | hp2 | a0002 | c0002 | t0005 | g0014 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02258 | hp1 | a0001 | c0003 | t0006 | g0061 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02258 | hp2 | a0002 | c0002 | t0005 | g0015 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02572 | hp1 | a0002 | c0002 | t0002 | g0199 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02572 | hp2 | a0001 | c0003 | t0006 | g0064 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02622 | hp1 | a0001 | c0003 | t0005 | g0017 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02630 | hp1 | a0002 | c0002 | t0005 | g0020 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02647 | hp2 | a0001 | c0003 | t0006 | g0062 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02683 | hp1 | a0001 | c0001 | t0004 | g0031 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02717 | hp1 | a0002 | c0002 | t0016 | g0135 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02717 | hp2 | a0001 | c0003 | t0006 | g0054 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02723 | hp1 | a0001 | c0004 | t0001 | g0130 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0132 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02818 | hp1 | a0002 | c0002 | t0005 | g0019 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02886 | hp1 | a0001 | c0003 | t0002 | g0057 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0295 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02895 | hp2 | a0001 | c0003 | t0012 | g0301 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02896 | hp2 | a0001 | c0003 | t0002 | g0050 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02897 | hp1 | a0001 | c0003 | t0002 | g0049 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02897 | hp2 | a0001 | c0003 | t0012 | g0302 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02922 | hp1 | a0002 | c0002 | t0005 | g0016 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02922 | hp2 | a0001 | c0003 | t0002 | g0048 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02965 | hp1 | a0001 | c0003 | t0020 | g0039 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0079 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02970 | hp2 | a0001 | c0003 | t0002 | g0002 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02976 | hp1 | a0001 | c0001 | t0026 | g0254 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02976 | hp2 | a0002 | c0002 | t0005 | g0021 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0111 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0086 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0131 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03098 | hp1 | a0002 | c0002 | t0005 | g0022 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03098 | hp2 | a0001 | c0004 | t0001 | g0088 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03130 | hp1 | a0001 | c0003 | t0002 | g0060 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0127 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03139 | hp1 | a0002 | c0002 | t0005 | g0018 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03139 | hp2 | a0001 | c0003 | t0002 | g0065 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0123 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03209 | hp2 | a0002 | c0002 | t0002 | g0083 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03225 | hp1 | a0001 | c0003 | t0006 | g0055 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0087 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03453 | hp1 | a0001 | c0003 | t0006 | g0052 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03491 | hp1 | a0001 | c0003 | t0009 | g0190 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03492 | hp2 | a0001 | c0003 | t0009 | g0224 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03516 | hp1 | a0002 | c0002 | t0024 | g0045 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0080 | AFR | ESN | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03540 | hp1 | a0002 | c0002 | t0017 | g0193 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03540 | hp2 | a0002 | c0002 | t0016 | g0134 | AFR | GWD | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03579 | hp1 | a0001 | c0003 | t0028 | g0051 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03688 | hp1 | a0001 | c0003 | t0009 | g0225 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0114 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03710 | hp2 | a0001 | c0001 | t0015 | g0040 | SAS | PJL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0315 | SAS | BEB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0319 | SAS | BEB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04184 | hp2 | a0001 | c0001 | t0015 | g0041 | SAS | BEB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04199 | hp1 | a0002 | c0002 | t0007 | g0009 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04204 | hp1 | a0001 | c0001 | t0030 | g0327 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0312 | SAS | STU | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0074 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18612 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | CHB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18906 | hp1 | a0001 | c0003 | t0002 | g0002 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18906 | hp2 | a0001 | c0005 | t0001 | g0042 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18947 | hp2 | a0002 | c0002 | t0007 | g0011 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18949 | hp2 | a0002 | c0002 | t0010 | g0122 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18950 | hp1 | a0002 | c0002 | t0018 | g0012 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18953 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18969 | hp1 | a0001 | c0001 | t0014 | g0323 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18970 | hp1 | a0002 | c0002 | t0007 | g0010 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18970 | hp2 | a0002 | c0002 | t0010 | g0004 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18972 | hp1 | a0001 | c0001 | t0023 | g0167 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18975 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18977 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18983 | hp1 | a0001 | c0001 | t0014 | g0325 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18998 | hp1 | a0002 | c0002 | t0010 | g0121 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18998 | hp2 | a0001 | c0006 | t0001 | g0069 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19003 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19004 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19006 | hp1 | a0001 | c0001 | t0029 | g0326 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19006 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0085 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19030 | hp2 | a0001 | c0003 | t0013 | g0303 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0077 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19043 | hp2 | a0001 | c0003 | t0002 | g0059 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19077 | hp2 | a0004 | c0007 | t0001 | g0185 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19088 | hp2 | a0001 | c0008 | t0001 | g0276 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19089 | hp2 | a0001 | c0001 | t0014 | g0324 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19091 | hp2 | a0002 | c0002 | t0010 | g0004 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19240 | hp1 | a0001 | c0003 | t0002 | g0058 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20129 | hp1 | a0001 | c0003 | t0013 | g0007 | AFR | ASW | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0228 | AFR | ASW | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20752 | hp2 | a0003 | c0009 | t0002 | g0078 | EUR | TSI | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | GIH | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | GIH | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02486 | hp1 | a0001 | c0003 | t0012 | g0304 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02486 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02559 | hp1 | a0001 | c0003 | t0006 | g0053 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03471 | hp1 | a0002 | c0002 | t0017 | g0230 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG03471 | hp2 | a0002 | c0002 | t0005 | g0023 | AFR | MSL | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG06807 | hp1 | a0001 | c0003 | t0013 | g0007 | AFR | USA | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA18955 | hp2 | a0002 | c0002 | t0007 | g0008 | EAS | JPT | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | USA | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | USA | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | LWK | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0232 | REF | REF | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0165 | REF | REF | CHD1_chr5_98848985_98934007 | CHD1 | chr5 | 98848985 | 98934007 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:98856460
|
AAGG | A | 2 | a0002a0003 | 72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
conservative_inframe_deletion | MODERATE | c.5050_5052delCCT | p.Pro1684del | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 5669/8145 | 5050/5133 | 1684/1710 | chr5 | 98856460 | ||
chr5:98869828
|
T | C | 1 | a0003 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.4033A>G | p.Ile1345Val | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/36 | 4650/8145 | 4033/5133 | 1345/1710 | chr5 | 98869828 | ||
chr5:98872160
|
A | G | 1 | a0004 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.3752T>C | p.Ile1251Thr | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/36 | 4369/8145 | 3752/5133 | 1251/1710 | chr5 | 98872160 | ||
chr5:98892699
|
T | A | 1 | a0005 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.2006A>T | p.Glu669Val | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/36 | 2623/8145 | 2006/5133 | 669/1710 | chr5 | 98892699 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:98856658
|
A | G | 1 | a0001c0004 | 6 | HG02723.hp1 HG03041.hp1 HG03098.hp2 others(3): Show |
synonymous_variant | LOW | c.4855T>C | p.Leu1619Leu | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 5472/8145 | 4855/5133 | 1619/1710 | chr5 | 98856658 | ||
chr5:98856707
|
C | T | 1 | a0001c0008 | 1 | NA19088.hp2 | synonymous_variant | LOW | c.4806G>A | p.Glu1602Glu | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 5423/8145 | 4806/5133 | 1602/1710 | chr5 | 98856707 | ||
chr5:98863500
|
C | T | 3 | a0001c0003a0002c0002a0003c0009 | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
synonymous_variant | LOW | c.4335G>A | p.Glu1445Glu | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/36 | 4952/8145 | 4335/5133 | 1445/1710 | chr5 | 98863500 | ||
chr5:98882064
|
C | T | 1 | a0001c0006 | 1 | NA18998.hp2 | synonymous_variant | LOW | c.2778G>A | p.Ala926Ala | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/36 | 3395/8145 | 2778/5133 | 926/1710 | chr5 | 98882064 | ||
chr5:98897315
|
T | C | 1 | a0001c0005 | 2 | HG01255.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.1371A>G | p.Leu457Leu | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/36 | 1988/8145 | 1371/5133 | 457/1710 | chr5 | 98897315 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:98853995
|
A | T | 1 | a0001c0005t0022 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2385T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2385 | chr5 | 98853995 | |||||
chr5:98854071
|
A | G | 1 | a0002c0002t0017 | 2 | HG03471.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2309T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2309 | chr5 | 98854071 | |||||
chr5:98854077
|
G | A | 1 | a0001c0001t0023 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2303C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2303 | chr5 | 98854077 | |||||
chr5:98854175
|
T | TCTTA | 19 | a0001c0003t0002a0001c0003t0005a0001c0003t0006others(16): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2204_*2205insTAAG | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2204 | chr5 | 98854175 | |||||
chr5:98854187
|
C | CA | 19 | a0001c0003t0002a0001c0003t0005a0001c0003t0006others(16): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*2192dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2192 | chr5 | 98854187 | |||||
chr5:98854267
|
G | A | 1 | a0001c0003t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2113C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2113 | chr5 | 98854267 | |||||
chr5:98854349
|
C | CAATAG | 18 | a0001c0003t0002a0001c0003t0005a0001c0003t0006others(15): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2030_*2031insCTAT others(1): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 2030 | chr5 | 98854349 | |||||
chr5:98854754
|
C | T | 1 | a0002c0002t0016 | 2 | HG02717.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1626G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1626 | chr5 | 98854754 | |||||
chr5:98854868
|
G | A | 1 | a0002c0002t0024 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1512C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1512 | chr5 | 98854868 | |||||
chr5:98854908
|
A | G | 1 | a0001c0003t0006 | 9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1472T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1472 | chr5 | 98854908 | |||||
chr5:98854986
|
C | G | 1 | a0001c0001t0021 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1394G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1394 | chr5 | 98854986 | |||||
chr5:98855035
|
C | A | 1 | a0002c0002t0025 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1345G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1345 | chr5 | 98855035 | |||||
chr5:98855095
|
T | C | 1 | a0001c0001t0026 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1285A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1285 | chr5 | 98855095 | |||||
chr5:98855097
|
T | C | 1 | a0002c0002t0018 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1283A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1283 | chr5 | 98855097 | |||||
chr5:98855138
|
C | T | 1 | a0001c0003t0009 | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1242G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1242 | chr5 | 98855138 | |||||
chr5:98855327
|
T | A | 1 | a0001c0003t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1053A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 1053 | chr5 | 98855327 | |||||
chr5:98855948
|
G | C | 1 | a0001c0003t0013 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*432C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 432 | chr5 | 98855948 | |||||
chr5:98856013
|
T | C | 1 | a0002c0002t0011 | 3 | HG00323.hp1 HG01358.hp1 HG01515.hp1 |
3_prime_UTR_variant | MODIFIER | c.*367A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 367 | chr5 | 98856013 | |||||
chr5:98856032
|
T | C | 1 | a0001c0001t0027 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 348 | chr5 | 98856032 | |||||
chr5:98856045
|
G | A | 1 | a0001c0003t0028 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 335 | chr5 | 98856045 | |||||
chr5:98856327
|
T | C | 1 | a0002c0002t0010 | 4 | NA18949.hp2 NA18970.hp2 NA18998.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*53A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 36/36 | 53 | chr5 | 98856327 | |||||
chr5:98928589
|
C | G | 1 | a0001c0001t0015 | 2 | HG03710.hp2 HG04184.hp2 |
5_prime_UTR_variant | MODIFIER | c.-199G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2203 | chr5 | 98928589 | |||||
chr5:98928592
|
G | A | 2 | a0001c0003t0012a0001c0003t0013 | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-202C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2206 | chr5 | 98928592 | |||||
chr5:98928631
|
C | G | 1 | a0001c0003t0020 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-241G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2245 | chr5 | 98928631 | |||||
chr5:98928691
|
G | A | 1 | a0001c0001t0003 | 18 | HG00621.hp2 HG01515.hp2 HG01516.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-301C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2305 | chr5 | 98928691 | |||||
chr5:98928702
|
C | T | 1 | a0001c0001t0008 | 4 | NA18975.hp2 NA18977.hp1 NA19009.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-312G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2316 | chr5 | 98928702 | |||||
chr5:98928708
|
T | C | 1 | a0001c0001t0014 | 3 | NA18969.hp1 NA18983.hp1 NA19089.hp2 |
5_prime_UTR_variant | MODIFIER | c.-318A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2322 | chr5 | 98928708 | |||||
chr5:98928709
|
C | T | 1 | a0001c0001t0004 | 13 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-319G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2323 | chr5 | 98928709 | |||||
chr5:98928806
|
TCGC | T | 4 | a0001c0003t0005a0002c0002t0005a0002c0002t0007others(1): Show | 15 | HG02055.hp2 HG02258.hp2 HG02622.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-419_-417delGCG | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2421 | chr5 | 98928806 | |||||
chr5:98928834
|
C | T | 1 | a0001c0001t0019 | 1 | HG00408.hp1 | 5_prime_UTR_variant | MODIFIER | c.-444G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2448 | chr5 | 98928834 | |||||
chr5:98928849
|
T | G | 1 | a0001c0001t0029 | 1 | NA19006.hp1 | 5_prime_UTR_variant | MODIFIER | c.-459A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2463 | chr5 | 98928849 | |||||
chr5:98928962
|
G | A | 1 | a0001c0001t0030 | 1 | HG04204.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-572C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | chr5 | 98928962 | ||||||
chr5:98928971
|
G | T | 2 | a0002c0002t0007a0002c0002t0018 | 5 | HG04199.hp1 NA18947.hp2 NA18950.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-581C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/36 | 2585 | chr5 | 98928971 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:98856761
|
T | C | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.4788-36A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856761 | ||||||
chr5:98856790
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0240a0001c0001t0001g0245 | 3 | HG01928.hp1 HG02273.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.4788-65A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856790 | ||||||
chr5:98856841
|
T | C | 228 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.4788-116A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856841 | ||||||
chr5:98856859
|
AACTT | A | 6 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(3): Show | 6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4788-138_4788-135d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856859 | ||||||
chr5:98856878
|
A | T | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4788-153T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856878 | ||||||
chr5:98856880
|
A | T | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4788-155T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856880 | ||||||
chr5:98856887
|
G | A | 1 | a0001c0001t0004g0026 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4788-162C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856887 | ||||||
chr5:98856938
|
T | C | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4788-213A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98856938 | ||||||
chr5:98857117
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.4788-392T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857117 | ||||||
chr5:98857297
|
TGA | T | 3 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199 | 3 | HG02572.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4788-574_4788-573d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857297 | ||||||
chr5:98857365
|
AAG | A | 8 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(5): Show | 9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.4788-642_4788-641d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857365 | ||||||
chr5:98857460
|
C | T | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.4787+720G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857460 | ||||||
chr5:98857604
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.4787+576G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857604 | ||||||
chr5:98857605
|
G | A | 1 | a0002c0002t0005g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4787+575C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857605 | ||||||
chr5:98857766
|
T | A | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4787+414A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857766 | ||||||
chr5:98857952
|
A | G | 1 | a0001c0008t0001g0276 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4787+228T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98857952 | ||||||
chr5:98858090
|
T | C | 7 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(4): Show | 8 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.4787+90A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98858090 | ||||||
chr5:98858163
|
G | T | 18 | a0001c0001t0001g0159a0001c0001t0001g0166a0001c0001t0003g0305others(15): Show | 18 | HG00621.hp2 HG01515.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.4787+17C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 35/35 | chr5 | 98858163 | ||||||
chr5:98858398
|
A | G | 2 | a0002c0002t0002g0125a0002c0002t0002g0126 | 2 | HG01168.hp1 HG01169.hp1 |
splice_region_variant&intron_variant | LOW | c.4577-8T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858398 | ||||||
chr5:98858472
|
G | A | 4 | a0001c0001t0001g0222a0001c0001t0001g0262a0001c0001t0001g0263others(1): Show | 4 | HG01928.hp2 NA18948.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.4577-82C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858472 | ||||||
chr5:98858482
|
T | C | 5 | a0001c0003t0012g0301a0001c0003t0012g0302a0001c0003t0012g0304others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.4577-92A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858482 | ||||||
chr5:98858640
|
T | C | 1 | a0001c0001t0001g0178 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4577-250A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858640 | ||||||
chr5:98858758
|
T | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4576+206A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858758 | ||||||
chr5:98858788
|
G | T | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4576+176C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858788 | ||||||
chr5:98858885
|
T | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4576+79A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858885 | ||||||
chr5:98858914
|
T | A | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4576+50A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858914 | ||||||
chr5:98858915
|
A | T | 1 | a0002c0002t0002g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4576+49T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858915 | ||||||
chr5:98858930
|
T | A | 7 | a0002c0002t0002g0077a0002c0002t0002g0079a0002c0002t0002g0080others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.4576+34A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 34/35 | chr5 | 98858930 | ||||||
chr5:98859077
|
C | G | 105 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0003t0002g0002others(102): Show | 109 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.4525-62G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859077 | ||||||
chr5:98859184
|
C | T | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.4525-169G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859184 | ||||||
chr5:98859251
|
G | T | 1 | a0001c0001t0001g0216 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4525-236C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859251 | ||||||
chr5:98859277
|
T | C | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01099.hp1 HG01192.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.4525-262A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859277 | ||||||
chr5:98859298
|
T | C | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4525-283A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859298 | ||||||
chr5:98859362
|
T | C | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.4525-347A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859362 | ||||||
chr5:98859514
|
G | A | 21 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(18): Show | 21 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.4524+458C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859514 | ||||||
chr5:98859670
|
T | C | 21 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(18): Show | 21 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.4524+302A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859670 | ||||||
chr5:98859822
|
G | A | 6 | a0001c0003t0006g0052a0001c0003t0006g0055a0001c0003t0006g0061others(3): Show | 6 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4524+150C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859822 | ||||||
chr5:98859955
|
TATG | T | 5 | a0002c0002t0002g0079a0002c0002t0002g0080a0002c0002t0002g0081others(2): Show | 5 | HG02486.hp2 HG02965.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.4524+14_4524+16del others(3): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 33/35 | chr5 | 98859955 | ||||||
chr5:98860114
|
A | G | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4428-46T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98860114 | ||||||
chr5:98860478
|
T | C | 15 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0004g0024others(12): Show | 15 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(12): Show |
intron_variant | MODIFIER | c.4428-410A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98860478 | ||||||
chr5:98861120
|
T | TA | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4428-1053dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861120 | ||||||
chr5:98861179
|
G | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4428-1111C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861179 | ||||||
chr5:98861301
|
G | A | 1 | a0001c0001t0001g0264 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4428-1233C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861301 | ||||||
chr5:98861777
|
T | C | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4427+1631A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861777 | ||||||
chr5:98861793
|
T | A | 1 | a0002c0002t0007g0011 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4427+1615A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861793 | ||||||
chr5:98861795
|
C | T | 18 | a0001c0001t0001g0159a0001c0001t0001g0166a0001c0001t0003g0305others(15): Show | 18 | HG00621.hp2 HG01515.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.4427+1613G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98861795 | ||||||
chr5:98862026
|
G | A | 67 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(64): Show | 69 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.4427+1382C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862026 | ||||||
chr5:98862353
|
A | C | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4427+1055T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862353 | ||||||
chr5:98862364
|
C | A | 1 | a0001c0001t0001g0296 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4427+1044G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862364 | ||||||
chr5:98862443
|
G | C | 2 | a0001c0003t0013g0007a0001c0003t0013g0303 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.4427+965C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862443 | ||||||
chr5:98862854
|
G | T | 1 | a0001c0001t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4427+554C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98862854 | ||||||
chr5:98863344
|
CA | C | 101 | a0001c0001t0004g0035a0001c0001t0029g0326a0001c0003t0002g0002others(98): Show | 105 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.4427+63delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98863344 | ||||||
chr5:98863349
|
A | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0207 | 2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.4427+59T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98863349 | ||||||
chr5:98863373
|
T | C | 123 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0089others(120): Show | 123 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.4427+35A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 32/35 | chr5 | 98863373 | ||||||
chr5:98863690
|
C | A | 1 | a0001c0001t0001g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4249-104G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98863690 | ||||||
chr5:98863719
|
C | T | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.4249-133G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98863719 | ||||||
chr5:98864263
|
G | A | 1 | a0002c0002t0002g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4249-677C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864263 | ||||||
chr5:98864433
|
A | G | 1 | a0002c0002t0005g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4249-847T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864433 | ||||||
chr5:98864517
|
C | CA | 36 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0001g0068others(33): Show | 37 | HG00621.hp1 HG01243.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.4249-932dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | ||||||
chr5:98864517
|
C | CAA | 20 | a0001c0001t0001g0071a0001c0003t0002g0048a0001c0003t0002g0049others(17): Show | 21 | HG00323.hp1 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.4249-933_4249-932d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | ||||||
chr5:98864517
|
C | CAAA | 8 | a0001c0003t0002g0002a0001c0003t0002g0057a0001c0003t0002g0058others(5): Show | 9 | HG02486.hp1 HG02572.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.4249-934_4249-932d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | ||||||
chr5:98864517
|
CA | C | 12 | a0001c0001t0001g0188a0001c0001t0001g0247a0001c0001t0001g0299others(9): Show | 12 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.4249-932delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | ||||||
chr5:98864517
|
CAA | C | 29 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(26): Show | 31 | HG00642.hp1 HG00741.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.4249-933_4249-932d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | ||||||
chr5:98864517
|
CAAAAAAA others(3): Show |
C | 13 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0001g0091others(10): Show | 13 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4249-941_4249-932d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | ||||||
chr5:98864517
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0220a0001c0001t0001g0265a0001c0001t0001g0266others(1): Show | 4 | HG02818.hp2 HG02895.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.4249-943_4249-932d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864517 | ||||||
chr5:98864977
|
C | T | 3 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050 | 3 | HG02896.hp2 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4249-1391G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98864977 | ||||||
chr5:98865157
|
G | A | 1 | a0001c0006t0001g0069 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.4249-1571C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865157 | ||||||
chr5:98865370
|
A | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0097 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4249-1784T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865370 | ||||||
chr5:98865397
|
T | C | 1 | a0002c0002t0002g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4249-1811A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865397 | ||||||
chr5:98865950
|
TG | T | 228 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.4249-2365delC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865950 | ||||||
chr5:98865964
|
G | A | 228 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.4249-2378C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98865964 | ||||||
chr5:98866081
|
CT | C | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4248+2413delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866081 | ||||||
chr5:98866107
|
TAAAAAAC others(12): Show |
T | 1 | a0001c0001t0001g0163 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.4248+2369_4248+238 others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866107 | ||||||
chr5:98866145
|
C | T | 1 | a0001c0001t0003g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4248+2350G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866145 | ||||||
chr5:98866191
|
CAG | C | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.4248+2302_4248+230 others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866191 | ||||||
chr5:98866198
|
G | A | 2 | a0002c0002t0017g0193a0002c0002t0017g0230 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4248+2297C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866198 | ||||||
chr5:98866208
|
A | T | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4248+2287T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866208 | ||||||
chr5:98866313
|
A | C | 27 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(24): Show | 29 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.4248+2182T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866313 | ||||||
chr5:98866324
|
G | A | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4248+2171C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866324 | ||||||
chr5:98866514
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4248+1981A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866514 | ||||||
chr5:98866614
|
A | G | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4248+1881T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866614 | ||||||
chr5:98866659
|
G | T | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.4248+1836C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866659 | ||||||
chr5:98866821
|
A | C | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.4248+1674T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866821 | ||||||
chr5:98866863
|
T | G | 1 | a0001c0001t0001g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4248+1632A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98866863 | ||||||
chr5:98867018
|
A | G | 1 | a0001c0001t0004g0036 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4248+1477T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867018 | ||||||
chr5:98867236
|
A | T | 1 | a0001c0001t0001g0268 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4248+1259T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867236 | ||||||
chr5:98867558
|
A | ATG | 17 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0001g0091others(14): Show | 17 | HG00738.hp1 HG01192.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4248+935_4248+936d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867558 | ||||||
chr5:98867558
|
A | ATGTG | 13 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(10): Show | 15 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.4248+933_4248+936d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867558 | ||||||
chr5:98867558
|
A | ATGTGTG | 12 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.4248+931_4248+936d others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867558 | ||||||
chr5:98867568
|
G | A | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4248+927C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867568 | ||||||
chr5:98867578
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4248+917T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867578 | ||||||
chr5:98867580
|
A | G | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.4248+915T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867580 | ||||||
chr5:98867795
|
G | GT | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0046others(110): Show | 117 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.4248+699dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867795 | ||||||
chr5:98867795
|
G | GTT | 10 | a0001c0001t0001g0070a0001c0001t0001g0179a0001c0001t0001g0196others(7): Show | 10 | HG00738.hp2 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.4248+698_4248+699d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867795 | ||||||
chr5:98867795
|
GT | G | 62 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(59): Show | 64 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.4248+699delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98867795 | ||||||
chr5:98868016
|
A | G | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.4248+479T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868016 | ||||||
chr5:98868031
|
C | T | 1 | a0001c0001t0014g0323 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4248+464G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868031 | ||||||
chr5:98868060
|
A | T | 33 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(30): Show | 35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.4248+435T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868060 | ||||||
chr5:98868114
|
C | T | 15 | a0002c0002t0002g0295a0002c0002t0005g0014a0002c0002t0005g0015others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.4248+381G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868114 | ||||||
chr5:98868266
|
G | A | 13 | a0001c0001t0004g0024a0001c0001t0004g0025a0001c0001t0004g0026others(10): Show | 13 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(10): Show |
intron_variant | MODIFIER | c.4248+229C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868266 | ||||||
chr5:98868331
|
G | GA | 14 | a0001c0001t0001g0067a0001c0001t0001g0184a0001c0001t0001g0198others(11): Show | 14 | HG00741.hp1 HG02886.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.4248+163dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868331 | ||||||
chr5:98868331
|
GA | G | 23 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0084others(20): Show | 23 | HG01243.hp2 HG01496.hp2 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.4248+163delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 31/35 | chr5 | 98868331 | ||||||
chr5:98868753
|
T | C | 4 | a0001c0001t0001g0044a0001c0001t0001g0240a0001c0001t0001g0245others(1): Show | 4 | HG01928.hp1 HG02273.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.4108-118A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868753 | ||||||
chr5:98868823
|
T | A | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4108-188A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868823 | ||||||
chr5:98868865
|
C | T | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.4108-230G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868865 | ||||||
chr5:98868991
|
A | AT | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.4108-357dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868991 | ||||||
chr5:98868991
|
AT | A | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4108-357delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98868991 | ||||||
chr5:98869326
|
C | A | 73 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017others(70): Show | 75 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.4107+428G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869326 | ||||||
chr5:98869517
|
C | T | 7 | a0002c0002t0005g0022a0002c0002t0005g0023a0002c0002t0007g0008others(4): Show | 7 | HG03098.hp1 HG03471.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.4107+237G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869517 | ||||||
chr5:98869529
|
G | C | 1 | a0002c0002t0005g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4107+225C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869529 | ||||||
chr5:98869606
|
G | A | 1 | a0001c0003t0012g0304 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4107+148C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869606 | ||||||
chr5:98869607
|
T | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0128 | 3 | HG01192.hp2 HG02257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4107+147A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869607 | ||||||
chr5:98869615
|
T | TGC | 6 | a0001c0001t0001g0232a0001c0001t0003g0319a0001c0001t0004g0025others(3): Show | 6 | HG04184.hp1 NA18948.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.4107+137_4107+138d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869615 | ||||||
chr5:98869615
|
TGCGC | T | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.4107+135_4107+138d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869615 | ||||||
chr5:98869618
|
G | GCA | 6 | a0002c0002t0002g0199a0002c0002t0002g0295a0002c0002t0016g0134others(3): Show | 6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4107+135_4107+136i others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869618 | ||||||
chr5:98869618
|
G | GCACA | 3 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0005g0021 | 3 | HG02723.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4107+135_4107+136i others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869618 | ||||||
chr5:98869618
|
G | GCACACA | 8 | a0002c0002t0002g0074a0002c0002t0002g0077a0002c0002t0002g0079others(5): Show | 8 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.4107+135_4107+136i others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869618 | ||||||
chr5:98869620
|
G | A | 17 | a0002c0002t0002g0074a0002c0002t0002g0077a0002c0002t0002g0079others(14): Show | 17 | HG01243.hp1 HG01496.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.4107+134C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869620 | ||||||
chr5:98869620
|
G | GCA | 4 | a0002c0002t0011g0073a0002c0002t0011g0075a0002c0002t0011g0076others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.4107+133_4107+134i others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869620 | ||||||
chr5:98869620
|
GCGCACAC others(3): Show |
G | 13 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(10): Show | 13 | HG02055.hp2 HG02258.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.4107+124_4107+133d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869620 | ||||||
chr5:98869622
|
G | A | 24 | a0001c0001t0001g0268a0001c0003t0005g0017a0002c0002t0002g0072others(21): Show | 24 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.4107+132C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | ||||||
chr5:98869622
|
G | GCA | 95 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0084others(92): Show | 95 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.4107+130_4107+131d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | ||||||
chr5:98869622
|
G | GCACA | 35 | a0001c0001t0001g0071a0001c0001t0001g0150a0001c0001t0001g0152others(32): Show | 35 | HG00423.hp2 HG01099.hp1 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.4107+128_4107+131d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | ||||||
chr5:98869622
|
G | GCGCACAC others(1): Show |
3 | a0001c0001t0001g0097a0001c0005t0001g0042a0001c0005t0022g0043 | 3 | HG01255.hp1 HG02055.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4107+131_4107+132i others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | ||||||
chr5:98869622
|
GCA | G | 12 | a0001c0001t0001g0138a0001c0001t0001g0178a0001c0001t0001g0215others(9): Show | 12 | HG02698.hp2 HG03041.hp1 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.4107+130_4107+131d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | ||||||
chr5:98869622
|
GCACACAC others(3): Show |
G | 33 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(30): Show | 35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.4107+122_4107+131d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869622 | ||||||
chr5:98869624
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4107+130T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869624 | ||||||
chr5:98869685
|
T | A | 1 | a0002c0002t0002g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4107+69A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 30/35 | chr5 | 98869685 | ||||||
chr5:98869892
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.3979-10T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98869892 | ||||||
chr5:98869917
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3979-35G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98869917 | ||||||
chr5:98869925
|
A | T | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3979-43T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98869925 | ||||||
chr5:98870104
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.3979-222T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870104 | ||||||
chr5:98870318
|
C | G | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.3978+369G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870318 | ||||||
chr5:98870414
|
C | T | 12 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(9): Show | 12 | HG00423.hp2 HG02015.hp2 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.3978+273G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870414 | ||||||
chr5:98870419
|
G | A | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.3978+268C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870419 | ||||||
chr5:98870425
|
C | T | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3978+262G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870425 | ||||||
chr5:98870493
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3978+194G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870493 | ||||||
chr5:98870614
|
T | C | 2 | a0002c0002t0005g0019a0002c0002t0005g0020 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.3978+73A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 29/35 | chr5 | 98870614 | ||||||
chr5:98871054
|
C | CCT | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3862-252_3862-251i others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871054 | ||||||
chr5:98871055
|
A | T | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3862-252T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871055 | ||||||
chr5:98871062
|
T | A | 5 | a0001c0003t0012g0301a0001c0003t0012g0302a0001c0003t0012g0304others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3862-259A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871062 | ||||||
chr5:98871116
|
A | ATTTTTTT others(296): Show |
1 | a0002c0002t0017g0193 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3862-314_3862-313i others(305): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871116 | ||||||
chr5:98871117
|
T | C | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3862-314A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871117 | ||||||
chr5:98871153
|
G | A | 1 | a0002c0002t0002g0226 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3862-350C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871153 | ||||||
chr5:98871181
|
C | T | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3862-378G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871181 | ||||||
chr5:98871369
|
C | CA | 38 | a0001c0001t0001g0068a0001c0001t0001g0147a0001c0001t0001g0151others(35): Show | 39 | HG01167.hp1 HG01433.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.3862-567dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
C | CAAAAAAA others(7): Show |
1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3862-580_3862-567d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
CA | C | 99 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0090others(96): Show | 99 | HG00423.hp1 HG00621.hp2 HG00738.hp1 others(96): Show |
intron_variant | MODIFIER | c.3862-567delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
CAA | C | 15 | a0001c0003t0002g0049a0001c0003t0002g0050a0001c0003t0006g0053others(12): Show | 16 | HG00323.hp1 HG01243.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.3862-568_3862-567d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.3862-576_3862-567d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
CAAAAAAA others(4): Show |
C | 1 | a0002c0002t0010g0121 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.3862-577_3862-567d others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
CAAAAAAA others(5): Show |
C | 34 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(31): Show | 36 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.3862-578_3862-567d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0188a0001c0001t0001g0221 | 2 | NA18946.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3862-580_3862-567d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3862-581_3862-567d others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871369
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3862-582_3862-567d others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871369 | ||||||
chr5:98871572
|
G | A | 9 | a0002c0002t0002g0003a0002c0002t0002g0102a0002c0002t0002g0103others(6): Show | 10 | NA18944.hp1 NA18946.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.3861+479C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871572 | ||||||
chr5:98871801
|
T | A | 1 | a0001c0001t0001g0268 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3861+250A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871801 | ||||||
chr5:98871839
|
A | G | 2 | a0001c0005t0001g0042a0001c0005t0022g0043 | 2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3861+212T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 28/35 | chr5 | 98871839 | ||||||
chr5:98872696
|
T | C | 49 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0090others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.3572-141A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872696 | ||||||
chr5:98872725
|
A | T | 228 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.3572-170T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872725 | ||||||
chr5:98872860
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3572-305G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872860 | ||||||
chr5:98872874
|
G | A | 1 | a0001c0003t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3572-319C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872874 | ||||||
chr5:98872981
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3572-426G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98872981 | ||||||
chr5:98873054
|
C | T | 1 | a0002c0002t0005g0015 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3572-499G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873054 | ||||||
chr5:98873057
|
G | T | 2 | a0001c0003t0013g0007a0001c0003t0013g0303 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3572-502C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873057 | ||||||
chr5:98873072
|
C | G | 1 | a0001c0008t0001g0276 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.3572-517G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873072 | ||||||
chr5:98873293
|
CTGTG | C | 3 | a0001c0001t0001g0177a0001c0003t0002g0227a0001c0003t0002g0228 | 3 | HG00741.hp1 NA18978.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3571+296_3571+299d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873293 | ||||||
chr5:98873419
|
C | T | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.3571+174G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 26/35 | chr5 | 98873419 | ||||||
chr5:98874091
|
G | GATA | 227 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(224): Show | 231 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.3441-371_3441-369d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874091 | ||||||
chr5:98874092
|
A | G | 1 | a0001c0001t0001g0188 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3441-369T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874092 | ||||||
chr5:98874096
|
G | A | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3441-373C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874096 | ||||||
chr5:98874097
|
A | T | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3441-374T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874097 | ||||||
chr5:98874102
|
T | A | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3441-379A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874102 | ||||||
chr5:98874183
|
C | G | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3441-460G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874183 | ||||||
chr5:98874249
|
G | A | 1 | a0002c0002t0018g0012 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3441-526C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874249 | ||||||
chr5:98874323
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3441-600A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874323 | ||||||
chr5:98874396
|
A | T | 1 | a0001c0001t0001g0252 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3441-673T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874396 | ||||||
chr5:98874525
|
C | A | 1 | a0001c0001t0001g0098 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3440+547G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874525 | ||||||
chr5:98874537
|
T | TA | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0187others(8): Show | 11 | HG00621.hp1 HG00621.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.3440+534dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874537 | ||||||
chr5:98874537
|
TA | T | 190 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0089others(187): Show | 194 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.3440+534delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874537 | ||||||
chr5:98874585
|
G | C | 1 | a0001c0003t0012g0304 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3440+487C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874585 | ||||||
chr5:98874643
|
T | C | 104 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(101): Show | 108 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3440+429A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874643 | ||||||
chr5:98874692
|
A | G | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3440+380T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874692 | ||||||
chr5:98874716
|
G | GA | 9 | a0001c0003t0006g0052a0001c0003t0006g0053a0001c0003t0006g0054others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.3440+355dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874716 | ||||||
chr5:98874953
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3440+119C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874953 | ||||||
chr5:98874986
|
A | C | 122 | a0001c0001t0001g0044a0001c0001t0001g0084a0001c0001t0001g0089others(119): Show | 122 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.3440+86T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 25/35 | chr5 | 98874986 | ||||||
chr5:98875164
|
T | A | 104 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(101): Show | 108 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3399-51A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875164 | ||||||
chr5:98875361
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3399-248T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875361 | ||||||
chr5:98875501
|
A | G | 104 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(101): Show | 108 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.3399-388T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875501 | ||||||
chr5:98875635
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0217 | 2 | HG01346.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.3399-522C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875635 | ||||||
chr5:98875934
|
A | G | 1 | a0002c0002t0002g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3398+464T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98875934 | ||||||
chr5:98876011
|
C | T | 1 | a0002c0002t0002g0119 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3398+387G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876011 | ||||||
chr5:98876036
|
C | T | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3398+362G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876036 | ||||||
chr5:98876155
|
T | TA | 7 | a0001c0003t0006g0052a0001c0003t0006g0055a0001c0003t0006g0061others(4): Show | 7 | HG01109.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3398+242dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876155 | ||||||
chr5:98876186
|
C | T | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.3398+212G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876186 | ||||||
chr5:98876227
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3398+171A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876227 | ||||||
chr5:98876329
|
G | A | 14 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0001g0091others(11): Show | 14 | HG00738.hp1 HG01192.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.3398+69C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 24/35 | chr5 | 98876329 | ||||||
chr5:98876690
|
T | A | 1 | a0001c0001t0030g0327 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3238-132A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876690 | ||||||
chr5:98876811
|
C | A | 10 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0110others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.3238-253G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876811 | ||||||
chr5:98876825
|
A | C | 1 | a0001c0001t0001g0256 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3238-267T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876825 | ||||||
chr5:98876826
|
G | T | 1 | a0001c0001t0001g0256 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3238-268C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876826 | ||||||
chr5:98876831
|
G | T | 1 | a0001c0001t0001g0256 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3238-273C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876831 | ||||||
chr5:98876840
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3238-282T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876840 | ||||||
chr5:98876847
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3238-289A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876847 | ||||||
chr5:98876867
|
C | A | 72 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(69): Show | 72 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.3238-309G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876867 | ||||||
chr5:98876932
|
G | A | 1 | a0001c0003t0009g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3238-374C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98876932 | ||||||
chr5:98877269
|
A | C | 4 | a0001c0001t0001g0147a0001c0001t0001g0201a0001c0001t0001g0208others(1): Show | 4 | HG01167.hp1 HG01168.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.3238-711T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877269 | ||||||
chr5:98877374
|
G | T | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.3238-816C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877374 | ||||||
chr5:98877441
|
C | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0241 | 3 | NA18947.hp1 NA18991.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.3238-883G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877441 | ||||||
chr5:98877623
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0282 | 2 | HG04199.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.3238-1065C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877623 | ||||||
chr5:98877655
|
A | G | 4 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(1): Show | 4 | HG01496.hp2 HG02572.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.3238-1097T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877655 | ||||||
chr5:98877944
|
C | T | 1 | a0001c0003t0006g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3238-1386G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877944 | ||||||
chr5:98877959
|
C | T | 3 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199 | 3 | HG02572.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3238-1401G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98877959 | ||||||
chr5:98878287
|
T | C | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.3237+1265A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878287 | ||||||
chr5:98878301
|
C | T | 228 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.3237+1251G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878301 | ||||||
chr5:98878416
|
C | G | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | NA18948.hp1 NA18987.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.3237+1136G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878416 | ||||||
chr5:98878428
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3237+1124G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878428 | ||||||
chr5:98878449
|
A | C | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3237+1103T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878449 | ||||||
chr5:98878449
|
A | T | 3 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050 | 3 | HG02896.hp2 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3237+1103T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878449 | ||||||
chr5:98878469
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3237+1083A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878469 | ||||||
chr5:98878483
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.3237+1069G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878483 | ||||||
chr5:98878556
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3237+996C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878556 | ||||||
chr5:98878734
|
C | T | 2 | a0001c0005t0001g0042a0001c0005t0022g0043 | 2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3237+818G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878734 | ||||||
chr5:98878801
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.3237+751A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878801 | ||||||
chr5:98878886
|
G | A | 1 | a0002c0002t0002g0119 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3237+666C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878886 | ||||||
chr5:98878969
|
G | A | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3237+583C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98878969 | ||||||
chr5:98879343
|
A | C | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.3237+209T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98879343 | ||||||
chr5:98879523
|
T | C | 2 | a0001c0005t0001g0042a0001c0005t0022g0043 | 2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3237+29A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 23/35 | chr5 | 98879523 | ||||||
chr5:98879765
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3061-37C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98879765 | ||||||
chr5:98879780
|
A | G | 1 | a0001c0001t0003g0314 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3061-52T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98879780 | ||||||
chr5:98879813
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0029g0326 | 2 | NA18991.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.3061-85A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98879813 | ||||||
chr5:98879915
|
T | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0129 | 3 | HG00738.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.3061-187A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98879915 | ||||||
chr5:98880004
|
C | T | 33 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(30): Show | 35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.3061-276G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880004 | ||||||
chr5:98880052
|
C | G | 1 | a0001c0001t0001g0235 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3061-324G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880052 | ||||||
chr5:98880149
|
G | A | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3061-421C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880149 | ||||||
chr5:98880224
|
T | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0247a0005c0010t0001g0251 | 3 | HG01081.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.3061-496A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880224 | ||||||
chr5:98880313
|
T | C | 5 | a0001c0003t0012g0301a0001c0003t0012g0302a0001c0003t0012g0304others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3061-585A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880313 | ||||||
chr5:98880827
|
C | A | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01256.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3060+249G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 22/35 | chr5 | 98880827 | ||||||
chr5:98881252
|
C | CT | 22 | a0001c0001t0001g0206a0001c0001t0001g0219a0001c0001t0001g0279others(19): Show | 22 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.2964+26dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 21/35 | chr5 | 98881252 | ||||||
chr5:98881252
|
CT | C | 20 | a0001c0001t0001g0175a0001c0001t0001g0218a0001c0001t0001g0222others(17): Show | 21 | HG01070.hp2 HG01169.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.2964+26delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 21/35 | chr5 | 98881252 | ||||||
chr5:98881252
|
CTTTTTTT | C | 9 | a0001c0003t0006g0052a0001c0003t0006g0053a0001c0003t0006g0054others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2964+20_2964+26del others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 21/35 | chr5 | 98881252 | ||||||
chr5:98881276
|
T | A | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.2964+3A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 21/35 | chr5 | 98881276 | ||||||
chr5:98881411
|
A | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0221 | 2 | NA18946.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2868-36T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881411 | ||||||
chr5:98881411
|
A | T | 1 | a0001c0001t0001g0005 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2868-36T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881411 | ||||||
chr5:98881499
|
A | C | 1 | a0001c0001t0003g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2868-124T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881499 | ||||||
chr5:98881510
|
T | A | 1 | a0001c0004t0001g0086 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2868-135A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881510 | ||||||
chr5:98881512
|
CT | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2868-138delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881512 | ||||||
chr5:98881513
|
T | C | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2868-138A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881513 | ||||||
chr5:98881579
|
A | G | 2 | a0002c0002t0016g0134a0002c0002t0016g0135 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2868-204T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881579 | ||||||
chr5:98881626
|
C | T | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2868-251G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 20/35 | chr5 | 98881626 | ||||||
chr5:98882137
|
CAT | C | 3 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0129 | 3 | HG00738.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2719-16_2719-15del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882137 | ||||||
chr5:98882237
|
T | C | 1 | a0001c0001t0004g0031 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2719-114A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882237 | ||||||
chr5:98882341
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2719-218C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882341 | ||||||
chr5:98882418
|
TG | T | 67 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0233others(64): Show | 69 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.2719-296delC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882418 | ||||||
chr5:98882460
|
G | C | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2719-337C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882460 | ||||||
chr5:98882503
|
T | C | 1 | a0001c0003t0006g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2719-380A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882503 | ||||||
chr5:98882782
|
A | C | 8 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0001g0091others(5): Show | 8 | HG00738.hp1 HG01192.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2718+306T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882782 | ||||||
chr5:98882793
|
G | A | 1 | a0002c0002t0005g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2718+295C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882793 | ||||||
chr5:98882961
|
C | G | 1 | a0001c0001t0001g0005 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2718+127G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 19/35 | chr5 | 98882961 | ||||||
chr5:98883386
|
T | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2569-149A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883386 | ||||||
chr5:98883468
|
T | C | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2569-231A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883468 | ||||||
chr5:98883498
|
A | C | 1 | a0001c0001t0003g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2569-261T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883498 | ||||||
chr5:98883600
|
A | G | 4 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(1): Show | 4 | HG02071.hp1 HG02080.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.2569-363T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883600 | ||||||
chr5:98883629
|
G | T | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2569-392C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883629 | ||||||
chr5:98883824
|
TAA | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0229a0001c0001t0019g0013 | 3 | HG00408.hp1 HG00408.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.2569-589_2569-588d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883824 | ||||||
chr5:98883826
|
A | AATAT | 3 | a0001c0001t0003g0305a0001c0001t0003g0306a0001c0001t0003g0315 | 3 | HG01515.hp2 HG01517.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2569-593_2569-590d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
A | AATATAT | 3 | a0001c0001t0001g0166a0001c0001t0001g0280a0001c0008t0001g0276 | 3 | HG02970.hp1 NA18956.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2569-595_2569-590d others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
A | AATATATA others(7): Show |
1 | a0001c0001t0026g0254 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2569-603_2569-590d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
A | AATATATA others(9): Show |
2 | a0001c0001t0001g0151a0001c0003t0002g0228 | 2 | NA18973.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2569-605_2569-590d others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
AAT | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0071a0001c0001t0001g0223others(6): Show | 9 | HG01243.hp2 HG01928.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.2569-591_2569-590d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
AATAT | A | 9 | a0001c0001t0001g0170a0001c0001t0001g0172a0001c0001t0001g0174others(6): Show | 9 | HG02027.hp1 HG02523.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.2569-593_2569-590d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
AATATATA others(3): Show |
A | 5 | a0001c0003t0006g0052a0001c0003t0006g0055a0001c0003t0006g0061others(2): Show | 5 | HG01109.hp1 HG02258.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2569-599_2569-590d others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
AATATATA others(5): Show |
A | 9 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(6): Show | 10 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2569-601_2569-590d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
AATATATA others(7): Show |
A | 2 | a0001c0003t0002g0048a0001c0003t0009g0224 | 2 | HG02922.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2569-603_2569-590d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
AATATATA others(11): Show |
A | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2569-607_2569-590d others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883826
|
AATATATA others(13): Show |
A | 1 | a0002c0002t0011g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2569-609_2569-590d others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883826 | ||||||
chr5:98883842
|
TATATATA others(12): Show |
T | 15 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(12): Show | 16 | HG00642.hp1 HG01243.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.2569-624_2569-606d others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883842 | ||||||
chr5:98883843
|
ATATATAT others(12): Show |
A | 29 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(26): Show | 30 | HG00741.hp2 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2569-625_2569-607d others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883843 | ||||||
chr5:98883843
|
ATATATAT others(13): Show |
A | 2 | a0002c0002t0002g0105a0002c0002t0002g0126 | 2 | HG01168.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.2569-626_2569-607d others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883843 | ||||||
chr5:98883844
|
TATATATA others(8): Show |
T | 1 | a0001c0003t0009g0190 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2569-622_2569-608d others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883844 | ||||||
chr5:98883844
|
TATATATA others(10): Show |
T | 1 | a0002c0002t0002g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2569-624_2569-608d others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883844 | ||||||
chr5:98883845
|
ATATATAT others(10): Show |
A | 2 | a0002c0002t0016g0134a0002c0002t0016g0135 | 2 | HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2569-625_2569-609d others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883845 | ||||||
chr5:98883845
|
ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0221 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2569-627_2569-609d others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883845 | ||||||
chr5:98883847
|
ATATATAT others(8): Show |
A | 2 | a0001c0001t0001g0099a0001c0001t0001g0173 | 2 | HG01255.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2569-625_2569-611d others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883847 | ||||||
chr5:98883847
|
ATATATAT others(9): Show |
A | 2 | a0001c0003t0002g0049a0001c0003t0002g0050 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2569-626_2569-611d others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883847 | ||||||
chr5:98883847
|
ATATATAT others(11): Show |
A | 5 | a0001c0003t0012g0301a0001c0003t0012g0302a0002c0002t0002g0112others(2): Show | 5 | HG00735.hp1 HG02723.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2569-628_2569-611d others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883847 | ||||||
chr5:98883849
|
ATATATAT others(6): Show |
A | 1 | a0001c0003t0006g0066 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2569-625_2569-613d others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | ||||||
chr5:98883849
|
ATATATAT others(8): Show |
A | 2 | a0002c0002t0002g0199a0002c0002t0005g0021 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2569-627_2569-613d others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | ||||||
chr5:98883849
|
ATATATAT others(10): Show |
A | 1 | a0002c0002t0025g0133 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2569-629_2569-613d others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | ||||||
chr5:98883849
|
ATATATAT others(11): Show |
A | 1 | a0001c0003t0012g0304 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2569-630_2569-613d others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | ||||||
chr5:98883849
|
ATATATAT others(12): Show |
A | 2 | a0001c0003t0013g0007a0001c0003t0013g0303 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2569-631_2569-613d others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883849 | ||||||
chr5:98883850
|
TATATATA others(4): Show |
T | 1 | a0001c0003t0006g0062 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2569-624_2569-614d others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883850 | ||||||
chr5:98883851
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0004g0033a0001c0003t0006g0054 | 2 | HG00544.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2569-625_2569-615d others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883851 | ||||||
chr5:98883851
|
ATATATAT others(5): Show |
A | 3 | a0001c0001t0001g0169a0002c0002t0005g0019a0002c0002t0005g0020 | 3 | HG02630.hp1 HG02818.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2569-626_2569-615d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883851 | ||||||
chr5:98883851
|
ATATATAT others(7): Show |
A | 8 | a0002c0002t0005g0015a0002c0002t0005g0018a0002c0002t0005g0022others(5): Show | 8 | HG02258.hp2 HG03098.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.2569-628_2569-615d others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883851 | ||||||
chr5:98883853
|
ATATATAT others(5): Show |
A | 2 | a0002c0002t0005g0014a0002c0002t0005g0016 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2569-628_2569-617d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883853 | ||||||
chr5:98883855
|
ATATATAT others(5): Show |
A | 1 | a0002c0002t0007g0011 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2569-630_2569-619d others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883855 | ||||||
chr5:98883856
|
TATATA | T | 10 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0171others(7): Show | 10 | HG01099.hp2 HG02074.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2569-624_2569-620d others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883856 | ||||||
chr5:98883857
|
ATATAT | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0047a0001c0001t0001g0138others(35): Show | 40 | HG00423.hp1 HG00621.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.2569-625_2569-621d others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883857 | ||||||
chr5:98883857
|
ATATATT | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0098a0001c0001t0001g0143others(4): Show | 7 | HG01516.hp1 NA18957.hp2 NA19058.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-626_2569-621d others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883857 | ||||||
chr5:98883858
|
TATA | T | 10 | a0001c0001t0001g0070a0001c0001t0001g0201a0001c0001t0001g0208others(7): Show | 10 | HG00438.hp1 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2569-624_2569-622d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883858 | ||||||
chr5:98883859
|
A | T | 2 | a0001c0001t0029g0326a0001c0003t0009g0224 | 2 | HG03492.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2569-622T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883859 | ||||||
chr5:98883859
|
ATAT | A | 39 | a0001c0001t0001g0006a0001c0001t0001g0141a0001c0001t0001g0146others(36): Show | 40 | HG00423.hp2 HG00642.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.2569-625_2569-623d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883859 | ||||||
chr5:98883859
|
ATATT | A | 6 | a0001c0001t0001g0153a0001c0001t0001g0157a0001c0001t0001g0206others(3): Show | 6 | HG00438.hp2 HG00544.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.2569-626_2569-623d others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883859 | ||||||
chr5:98883859
|
ATATTT | A | 7 | a0001c0001t0001g0090a0001c0001t0001g0147a0001c0001t0001g0159others(4): Show | 7 | HG01167.hp1 HG02109.hp2 HG04204.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-627_2569-623d others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883859 | ||||||
chr5:98883861
|
A | ATATATAT others(14): Show |
1 | a0001c0003t0002g0227 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2569-625_2569-624i others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | ||||||
chr5:98883861
|
A | T | 19 | a0001c0001t0001g0180a0001c0001t0001g0210a0001c0001t0001g0223others(16): Show | 19 | HG01109.hp1 HG01358.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.2569-624T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | ||||||
chr5:98883861
|
AT | A | 15 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0129others(12): Show | 15 | HG00738.hp1 HG01070.hp2 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.2569-625delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | ||||||
chr5:98883861
|
ATT | A | 8 | a0001c0001t0001g0148a0001c0001t0001g0246a0001c0001t0001g0267others(5): Show | 8 | HG01255.hp1 HG01516.hp2 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.2569-626_2569-625d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | ||||||
chr5:98883861
|
ATTT | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00323.hp2 HG01192.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2569-627_2569-625d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883861 | ||||||
chr5:98883862
|
T | TA | 9 | a0001c0001t0001g0144a0001c0001t0001g0152a0001c0001t0001g0204others(6): Show | 9 | HG00621.hp2 HG01517.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.2569-626_2569-625i others(3): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883862 | ||||||
chr5:98883862
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0250 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2569-626_2569-625i others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883862 | ||||||
chr5:98883862
|
T | TATATATA others(8): Show |
1 | a0001c0001t0001g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2569-626_2569-625i others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883862 | ||||||
chr5:98883863
|
T | A | 18 | a0001c0001t0001g0068a0001c0001t0001g0151a0001c0001t0001g0166others(15): Show | 18 | HG01515.hp2 HG01517.hp2 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2569-626A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883863 | ||||||
chr5:98883864
|
T | A | 12 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0129others(9): Show | 12 | HG00738.hp1 HG01517.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2569-627A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883864 | ||||||
chr5:98883865
|
T | A | 9 | a0001c0001t0001g0068a0001c0001t0003g0305a0001c0001t0003g0306others(6): Show | 9 | HG01255.hp1 HG01515.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.2569-628A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883865 | ||||||
chr5:98883866
|
T | A | 7 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0128others(4): Show | 7 | HG00323.hp2 HG01192.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.2569-629A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883866 | ||||||
chr5:98883867
|
T | A | 4 | a0001c0001t0003g0305a0001c0001t0003g0306a0001c0001t0003g0307others(1): Show | 4 | HG01255.hp1 HG01515.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2569-630A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883867 | ||||||
chr5:98883868
|
T | A | 2 | a0001c0001t0001g0144a0001c0003t0009g0191 | 2 | HG00323.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2569-631A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883868 | ||||||
chr5:98883870
|
T | A | 1 | a0001c0001t0001g0144 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2569-633A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883870 | ||||||
chr5:98883889
|
A | G | 326 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0044others(323): Show | 333 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(330): Show |
intron_variant | MODIFIER | c.2569-652T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883889 | ||||||
chr5:98883926
|
C | CCACCT | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.2569-694_2569-690d others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98883926 | ||||||
chr5:98884078
|
G | GT | 20 | a0001c0001t0001g0161a0001c0001t0001g0204a0001c0001t0004g0034others(17): Show | 20 | HG00438.hp1 HG01496.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2569-842dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884078 | ||||||
chr5:98884097
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2569-860C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884097 | ||||||
chr5:98884142
|
C | T | 70 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(67): Show | 72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.2569-905G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884142 | ||||||
chr5:98884328
|
C | A | 1 | a0001c0001t0001g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2569-1091G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884328 | ||||||
chr5:98884509
|
G | GA | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2568+1068dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884509 | ||||||
chr5:98884520
|
A | AG | 5 | a0001c0001t0001g0154a0001c0001t0001g0275a0001c0003t0013g0303others(2): Show | 5 | HG01099.hp1 HG01496.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2568+1057dupC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884520 | ||||||
chr5:98884550
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2568+1028C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884550 | ||||||
chr5:98884785
|
T | C | 4 | a0001c0001t0001g0138a0001c0001t0001g0172a0001c0001t0001g0178others(1): Show | 4 | NA18953.hp1 NA18974.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2568+793A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884785 | ||||||
chr5:98884792
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2568+786G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884792 | ||||||
chr5:98884861
|
G | A | 71 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(68): Show | 71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.2568+717C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884861 | ||||||
chr5:98884927
|
T | A | 1 | a0001c0001t0027g0137 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2568+651A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98884927 | ||||||
chr5:98885196
|
G | A | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2568+382C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98885196 | ||||||
chr5:98885283
|
T | C | 34 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(31): Show | 34 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.2568+295A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 18/35 | chr5 | 98885283 | ||||||
chr5:98885679
|
A | AT | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2497-31_2497-30ins others(1): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98885679 | ||||||
chr5:98886015
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2497-366A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886015 | ||||||
chr5:98886029
|
C | A | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2497-380G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886029 | ||||||
chr5:98886077
|
G | C | 16 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(13): Show | 16 | HG00423.hp2 HG02015.hp2 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.2497-428C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886077 | ||||||
chr5:98886117
|
C | A | 1 | a0001c0003t0002g0059 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2497-468G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886117 | ||||||
chr5:98886558
|
G | A | 8 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(5): Show | 9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2497-909C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886558 | ||||||
chr5:98886697
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2497-1048G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886697 | ||||||
chr5:98886896
|
A | G | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2496+1192T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886896 | ||||||
chr5:98886939
|
G | C | 2 | a0001c0003t0002g0049a0001c0003t0002g0050 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2496+1149C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886939 | ||||||
chr5:98886957
|
TA | T | 6 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(3): Show | 6 | NA18947.hp1 NA18991.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.2496+1130delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98886957 | ||||||
chr5:98887108
|
C | T | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.2496+980G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887108 | ||||||
chr5:98887129
|
T | A | 2 | a0001c0003t0009g0190a0001c0003t0009g0224 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.2496+959A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887129 | ||||||
chr5:98887199
|
C | T | 11 | a0001c0001t0001g0169a0001c0001t0001g0179a0001c0001t0001g0183others(8): Show | 11 | HG00544.hp2 HG01981.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.2496+889G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887199 | ||||||
chr5:98887279
|
C | G | 2 | a0002c0002t0007g0008a0002c0002t0007g0010 | 2 | NA18955.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2496+809G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887279 | ||||||
chr5:98887322
|
T | G | 1 | a0001c0003t0012g0304 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2496+766A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887322 | ||||||
chr5:98887427
|
T | C | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496+661A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887427 | ||||||
chr5:98887546
|
T | C | 1 | a0002c0002t0007g0009 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2496+542A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887546 | ||||||
chr5:98887602
|
A | T | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496+486T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887602 | ||||||
chr5:98887603
|
G | T | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496+485C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887603 | ||||||
chr5:98887604
|
A | T | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2496+484T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887604 | ||||||
chr5:98887766
|
G | C | 6 | a0002c0002t0002g0003a0002c0002t0002g0103a0002c0002t0002g0104others(3): Show | 7 | NA18944.hp1 NA18946.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.2496+322C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887766 | ||||||
chr5:98887929
|
G | A | 1 | a0002c0002t0005g0015 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2496+159C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 17/35 | chr5 | 98887929 | ||||||
chr5:98888297
|
C | T | 1 | a0001c0001t0004g0031 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2344-57G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 16/35 | chr5 | 98888297 | ||||||
chr5:98888298
|
G | A | 1 | a0002c0002t0002g0118 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2344-58C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 16/35 | chr5 | 98888298 | ||||||
chr5:98888678
|
C | T | 6 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(3): Show | 6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2343+398G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 16/35 | chr5 | 98888678 | ||||||
chr5:98889010
|
C | T | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2343+66G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 16/35 | chr5 | 98889010 | ||||||
chr5:98889271
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2181-33C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98889271 | ||||||
chr5:98889516
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2181-278C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98889516 | ||||||
chr5:98889582
|
AT | A | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.2181-345delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98889582 | ||||||
chr5:98889659
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2181-421T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98889659 | ||||||
chr5:98890053
|
G | T | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.2181-815C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890053 | ||||||
chr5:98890062
|
A | T | 1 | a0001c0001t0001g0219 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2181-824T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890062 | ||||||
chr5:98890177
|
T | C | 1 | a0001c0001t0003g0307 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2181-939A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890177 | ||||||
chr5:98890455
|
A | G | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2181-1217T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890455 | ||||||
chr5:98890733
|
T | C | 3 | a0001c0003t0006g0053a0001c0003t0006g0054a0001c0003t0006g0062 | 3 | HG02559.hp1 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2181-1495A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890733 | ||||||
chr5:98890762
|
T | C | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.2181-1524A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890762 | ||||||
chr5:98890775
|
G | C | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2181-1537C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890775 | ||||||
chr5:98890859
|
C | G | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2181-1621G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890859 | ||||||
chr5:98890958
|
G | A | 3 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050 | 3 | HG02896.hp2 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2180+1567C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98890958 | ||||||
chr5:98891399
|
A | G | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2180+1126T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891399 | ||||||
chr5:98891661
|
A | G | 1 | a0001c0003t0006g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2180+864T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891661 | ||||||
chr5:98891798
|
G | C | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2180+727C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891798 | ||||||
chr5:98891808
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2180+717G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891808 | ||||||
chr5:98891846
|
A | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2180+679T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891846 | ||||||
chr5:98891932
|
T | C | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.2180+593A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891932 | ||||||
chr5:98891982
|
A | G | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2180+543T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98891982 | ||||||
chr5:98892108
|
C | T | 1 | a0002c0002t0002g0115 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2180+417G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98892108 | ||||||
chr5:98892164
|
C | G | 5 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(2): Show | 6 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2180+361G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98892164 | ||||||
chr5:98892181
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2180+344C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 15/35 | chr5 | 98892181 | ||||||
chr5:98892837
|
T | A | 1 | a0001c0003t0009g0225 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1992-124A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98892837 | ||||||
chr5:98893074
|
T | C | 4 | a0001c0001t0001g0098a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | NA19005.hp2 NA19058.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.1991+342A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893074 | ||||||
chr5:98893235
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1991+181T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893235 | ||||||
chr5:98893255
|
T | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1991+161A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893255 | ||||||
chr5:98893265
|
C | A | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.1991+151G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893265 | ||||||
chr5:98893285
|
T | A | 9 | a0001c0003t0006g0052a0001c0003t0006g0053a0001c0003t0006g0054others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1991+131A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893285 | ||||||
chr5:98893400
|
T | C | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.1991+16A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 14/35 | chr5 | 98893400 | ||||||
chr5:98893645
|
G | A | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1801-39C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893645 | ||||||
chr5:98893682
|
A | T | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1801-76T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893682 | ||||||
chr5:98893824
|
C | A | 1 | a0001c0001t0004g0031 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1801-218G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893824 | ||||||
chr5:98893836
|
T | C | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1801-230A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893836 | ||||||
chr5:98893859
|
C | T | 1 | a0001c0003t0020g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1801-253G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893859 | ||||||
chr5:98893911
|
A | T | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1801-305T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893911 | ||||||
chr5:98893926
|
C | T | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1801-320G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98893926 | ||||||
chr5:98894010
|
C | T | 21 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(18): Show | 21 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1801-404G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894010 | ||||||
chr5:98894116
|
C | CT | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | NA18948.hp1 NA18987.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1800+480dupA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894116 | ||||||
chr5:98894313
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1800+284G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894313 | ||||||
chr5:98894473
|
A | G | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1800+124T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894473 | ||||||
chr5:98894517
|
T | C | 50 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0090others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.1800+80A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894517 | ||||||
chr5:98894567
|
G | C | 1 | a0002c0002t0007g0011 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1800+30C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 13/35 | chr5 | 98894567 | ||||||
chr5:98894752
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1711-66T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98894752 | ||||||
chr5:98894826
|
G | T | 1 | a0001c0001t0003g0316 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1711-140C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98894826 | ||||||
chr5:98894844
|
A | T | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1711-158T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98894844 | ||||||
chr5:98894914
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1711-228G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98894914 | ||||||
chr5:98895010
|
A | T | 1 | a0001c0001t0001g0005 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1711-324T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895010 | ||||||
chr5:98895026
|
G | C | 1 | a0001c0001t0001g0184 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1711-340C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895026 | ||||||
chr5:98895262
|
TAA | T | 29 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(26): Show | 31 | HG00741.hp1 HG01109.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1711-578_1711-577d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895262 | ||||||
chr5:98895291
|
G | C | 1 | a0002c0002t0005g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1711-605C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895291 | ||||||
chr5:98895450
|
T | G | 1 | a0001c0001t0004g0036 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1711-764A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895450 | ||||||
chr5:98895523
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1710+703G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895523 | ||||||
chr5:98895745
|
C | CA | 14 | a0001c0001t0001g0248a0001c0001t0001g0268a0001c0001t0001g0282others(11): Show | 14 | HG00323.hp2 HG01109.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1710+480dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895745 | ||||||
chr5:98895745
|
CA | C | 8 | a0001c0001t0001g0250a0001c0001t0001g0252a0001c0001t0001g0253others(5): Show | 8 | HG01891.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710+480delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895745 | ||||||
chr5:98895759
|
C | A | 8 | a0002c0002t0002g0074a0002c0002t0002g0077a0002c0002t0002g0079others(5): Show | 8 | HG01243.hp1 HG02486.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710+467G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98895759 | ||||||
chr5:98896006
|
C | T | 3 | a0001c0001t0001g0239a0001c0001t0001g0249a0001c0001t0001g0268 | 3 | NA19011.hp1 NA19075.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1710+220G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98896006 | ||||||
chr5:98896073
|
C | T | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1710+153G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98896073 | ||||||
chr5:98896111
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1710+115A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 12/35 | chr5 | 98896111 | ||||||
chr5:98896451
|
T | A | 1 | a0001c0001t0001g0152 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1494-9A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896451 | ||||||
chr5:98896540
|
A | T | 3 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199 | 3 | HG02572.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1494-98T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896540 | ||||||
chr5:98896569
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1494-127G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896569 | ||||||
chr5:98896595
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1494-153A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896595 | ||||||
chr5:98896655
|
C | T | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1494-213G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896655 | ||||||
chr5:98896775
|
T | C | 1 | a0001c0001t0003g0308 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1494-333A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896775 | ||||||
chr5:98896791
|
T | TA | 324 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0044others(321): Show | 331 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.1494-350dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896791 | ||||||
chr5:98896850
|
T | C | 71 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(68): Show | 71 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(68): Show |
intron_variant | MODIFIER | c.1493+343A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98896850 | ||||||
chr5:98897020
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1493+173C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98897020 | ||||||
chr5:98897069
|
A | G | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG02818.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1493+124T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98897069 | ||||||
chr5:98897105
|
T | C | 105 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0003t0002g0002others(102): Show | 109 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.1493+88A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 11/35 | chr5 | 98897105 | ||||||
chr5:98897364
|
A | G | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1366-44T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98897364 | ||||||
chr5:98897435
|
T | A | 2 | a0001c0003t0009g0190a0001c0003t0009g0224 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1366-115A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98897435 | ||||||
chr5:98898019
|
T | C | 22 | a0001c0001t0008g0038a0002c0002t0002g0131a0002c0002t0002g0132others(19): Show | 22 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1365+237A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898019 | ||||||
chr5:98898023
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1365+233G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898023 | ||||||
chr5:98898047
|
T | TAA | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.1365+207_1365+208d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898047 | ||||||
chr5:98898215
|
A | G | 10 | a0001c0001t0001g0169a0001c0001t0001g0179a0001c0001t0001g0183others(7): Show | 10 | HG00544.hp2 HG01981.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1365+41T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898215 | ||||||
chr5:98898228
|
A | G | 9 | a0001c0003t0006g0052a0001c0003t0006g0053a0001c0003t0006g0054others(6): Show | 9 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1365+28T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 10/35 | chr5 | 98898228 | ||||||
chr5:98898556
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1186+108A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 9/35 | chr5 | 98898556 | ||||||
chr5:98899097
|
C | G | 1 | a0001c0001t0001g0269 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1086-333G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 8/35 | chr5 | 98899097 | ||||||
chr5:98899228
|
C | T | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085+252G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 8/35 | chr5 | 98899228 | ||||||
chr5:98899309
|
G | T | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085+171C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 8/35 | chr5 | 98899309 | ||||||
chr5:98899397
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1085+83A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 8/35 | chr5 | 98899397 | ||||||
chr5:98899751
|
T | C | 2 | a0002c0002t0017g0193a0002c0002t0017g0230 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.860-46A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98899751 | ||||||
chr5:98899879
|
G | A | 2 | a0002c0002t0002g0295a0002c0002t0005g0021 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.860-174C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98899879 | ||||||
chr5:98899909
|
G | A | 1 | a0002c0002t0002g0116 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.860-204C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98899909 | ||||||
chr5:98900007
|
G | A | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.860-302C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900007 | ||||||
chr5:98900192
|
G | A | 4 | a0001c0004t0001g0086a0001c0004t0001g0087a0001c0004t0001g0088others(1): Show | 4 | HG03041.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-487C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900192 | ||||||
chr5:98900259
|
A | G | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.859+552T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900259 | ||||||
chr5:98900281
|
CA | C | 96 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(93): Show | 100 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.859+529delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900281 | ||||||
chr5:98900441
|
CT | C | 15 | a0001c0001t0001g0095a0001c0001t0003g0320a0002c0002t0005g0014others(12): Show | 15 | HG02055.hp2 HG02258.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.859+369delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900441 | ||||||
chr5:98900471
|
G | A | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.859+340C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900471 | ||||||
chr5:98900586
|
C | T | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+225G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900586 | ||||||
chr5:98900697
|
C | T | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.859+114G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900697 | ||||||
chr5:98900703
|
C | T | 6 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0236others(3): Show | 6 | HG00642.hp2 HG01070.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.859+108G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900703 | ||||||
chr5:98900705
|
G | GC | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.859+105dupG | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900705 | ||||||
chr5:98900708
|
C | A | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.859+103G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 7/35 | chr5 | 98900708 | ||||||
chr5:98901127
|
T | C | 72 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(69): Show | 72 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.588-45A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 6/35 | chr5 | 98901127 | ||||||
chr5:98901479
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0282 | 2 | HG04199.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.438-144T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901479 | ||||||
chr5:98901551
|
A | G | 1 | a0001c0001t0030g0327 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.438-216T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901551 | ||||||
chr5:98901654
|
T | C | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.438-319A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901654 | ||||||
chr5:98901694
|
C | A | 1 | a0002c0002t0005g0015 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.438-359G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901694 | ||||||
chr5:98901749
|
T | TA | 74 | a0001c0001t0003g0305a0001c0001t0003g0306a0001c0003t0009g0190others(71): Show | 76 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.438-415dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901749 | ||||||
chr5:98901749
|
TA | T | 19 | a0001c0001t0001g0198a0001c0001t0001g0279a0001c0003t0002g0048others(16): Show | 20 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.438-415delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901749 | ||||||
chr5:98901780
|
A | G | 1 | a0002c0002t0002g0083 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.438-445T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901780 | ||||||
chr5:98901884
|
T | C | 1 | a0001c0003t0009g0191 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.438-549A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901884 | ||||||
chr5:98901898
|
G | T | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.438-563C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98901898 | ||||||
chr5:98902104
|
C | T | 1 | a0001c0004t0001g0088 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.438-769G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902104 | ||||||
chr5:98902372
|
A | C | 12 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.437+528T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902372 | ||||||
chr5:98902430
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.437+470C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902430 | ||||||
chr5:98902499
|
C | A | 4 | a0002c0002t0002g0079a0002c0002t0002g0080a0002c0002t0002g0082others(1): Show | 4 | HG02486.hp2 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+401G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902499 | ||||||
chr5:98902672
|
G | T | 5 | a0001c0003t0012g0301a0001c0003t0012g0302a0001c0003t0012g0304others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.437+228C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 5/35 | chr5 | 98902672 | ||||||
chr5:98902979
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.373-15A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98902979 | ||||||
chr5:98902989
|
A | T | 1 | a0002c0002t0017g0230 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.373-25T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98902989 | ||||||
chr5:98903136
|
T | C | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.373-172A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903136 | ||||||
chr5:98903225
|
A | T | 18 | a0001c0001t0003g0305a0001c0001t0003g0306a0001c0001t0003g0307others(15): Show | 18 | HG00621.hp2 HG01515.hp2 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.373-261T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903225 | ||||||
chr5:98903308
|
TTGTTA | T | 5 | a0002c0002t0007g0008a0002c0002t0007g0009a0002c0002t0007g0010others(2): Show | 5 | HG04199.hp1 NA18947.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-349_373-345del others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903308 | ||||||
chr5:98903325
|
G | A | 2 | a0001c0003t0013g0007a0001c0003t0013g0303 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.373-361C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903325 | ||||||
chr5:98903438
|
TTTCGTAC others(27): Show |
T | 14 | a0001c0001t0001g0084a0001c0001t0001g0090a0001c0001t0001g0091others(11): Show | 14 | HG00738.hp1 HG01192.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.372+320_372+353del others(34): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903438 | ||||||
chr5:98903442
|
G | A | 1 | a0001c0005t0001g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.372+350C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903442 | ||||||
chr5:98903566
|
G | A | 1 | a0001c0001t0001g0178 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.372+226C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903566 | ||||||
chr5:98903686
|
C | T | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+106G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 4/35 | chr5 | 98903686 | ||||||
chr5:98904096
|
A | G | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-188T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904096 | ||||||
chr5:98904190
|
G | A | 2 | a0002c0002t0002g0120a0002c0002t0002g0195 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.256-282C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904190 | ||||||
chr5:98904318
|
T | G | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.256-410A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904318 | ||||||
chr5:98904348
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.256-440T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904348 | ||||||
chr5:98904387
|
C | A | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.256-479G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904387 | ||||||
chr5:98904460
|
C | G | 6 | a0001c0001t0003g0314a0001c0001t0003g0316a0001c0001t0003g0317others(3): Show | 6 | HG00621.hp2 HG02027.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+437G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904460 | ||||||
chr5:98904579
|
T | C | 1 | a0001c0001t0019g0013 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.255+318A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904579 | ||||||
chr5:98904769
|
A | G | 1 | a0002c0002t0017g0230 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.255+128T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 3/35 | chr5 | 98904769 | ||||||
chr5:98905343
|
A | G | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-245T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905343 | ||||||
chr5:98905361
|
A | G | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-263T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905361 | ||||||
chr5:98905524
|
TA | T | 70 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(67): Show | 72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.54-427delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905524 | ||||||
chr5:98905733
|
T | C | 1 | a0002c0002t0002g0109 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.54-635A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905733 | ||||||
chr5:98905785
|
G | A | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.54-687C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98905785 | ||||||
chr5:98906014
|
A | G | 17 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(14): Show | 18 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.54-916T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906014 | ||||||
chr5:98906045
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0129 | 3 | HG00738.hp1 HG03579.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.54-947G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906045 | ||||||
chr5:98906095
|
CTT | C | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-999_54-998delAA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906095 | ||||||
chr5:98906478
|
G | A | 5 | a0001c0003t0012g0301a0001c0003t0012g0302a0001c0003t0012g0304others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-1380C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906478 | ||||||
chr5:98906499
|
T | C | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.54-1401A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98906499 | ||||||
chr5:98907418
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.54-2320C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907418 | ||||||
chr5:98907471
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.54-2373G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907471 | ||||||
chr5:98907531
|
T | C | 1 | a0001c0001t0003g0313 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.54-2433A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907531 | ||||||
chr5:98907588
|
C | CA | 164 | a0001c0001t0001g0044a0001c0001t0001g0188a0001c0001t0001g0216others(161): Show | 168 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.54-2491dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907588 | ||||||
chr5:98907588
|
C | CAA | 11 | a0001c0001t0001g0231a0002c0002t0002g0080a0002c0002t0002g0100others(8): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.54-2492_54-2491dup others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907588 | ||||||
chr5:98907663
|
T | G | 1 | a0001c0001t0001g0084 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.54-2565A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907663 | ||||||
chr5:98907672
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0006t0001g0069 | 3 | HG02083.hp2 NA18998.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.54-2574T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907672 | ||||||
chr5:98907698
|
T | C | 1 | a0001c0001t0001g0259 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.54-2600A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907698 | ||||||
chr5:98907707
|
C | T | 8 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(5): Show | 9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-2609G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907707 | ||||||
chr5:98907836
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.54-2738T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98907836 | ||||||
chr5:98908115
|
T | G | 1 | a0001c0001t0015g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.54-3017A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908115 | ||||||
chr5:98908136
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.54-3038A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908136 | ||||||
chr5:98908236
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.54-3138G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908236 | ||||||
chr5:98908760
|
C | T | 3 | a0002c0002t0002g0102a0002c0002t0002g0118a0002c0002t0002g0192 | 3 | NA18965.hp2 NA18981.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.54-3662G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908760 | ||||||
chr5:98908800
|
G | GAATA | 228 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.54-3706_54-3703dup others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908800 | ||||||
chr5:98908883
|
T | C | 5 | a0001c0003t0012g0301a0001c0003t0012g0302a0001c0003t0012g0304others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-3785A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98908883 | ||||||
chr5:98909014
|
C | CATGAA | 21 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(18): Show | 21 | HG01496.hp2 HG02055.hp2 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.54-3921_54-3917dup others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909014 | ||||||
chr5:98909054
|
C | G | 1 | a0001c0001t0001g0176 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.54-3956G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909054 | ||||||
chr5:98909193
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.54-4095C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909193 | ||||||
chr5:98909318
|
T | C | 1 | a0001c0001t0003g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.54-4220A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909318 | ||||||
chr5:98909413
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.54-4315A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909413 | ||||||
chr5:98909538
|
T | C | 72 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(69): Show | 72 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.54-4440A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909538 | ||||||
chr5:98909555
|
A | G | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-4457T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909555 | ||||||
chr5:98909577
|
C | T | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-4479G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909577 | ||||||
chr5:98909608
|
C | T | 6 | a0001c0003t0006g0052a0001c0003t0006g0055a0001c0003t0006g0061others(3): Show | 6 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-4510G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909608 | ||||||
chr5:98909750
|
T | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.54-4652A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909750 | ||||||
chr5:98909802
|
T | G | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.54-4704A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909802 | ||||||
chr5:98909848
|
C | T | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.54-4750G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98909848 | ||||||
chr5:98910073
|
T | C | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.54-4975A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910073 | ||||||
chr5:98910129
|
G | A | 2 | a0002c0002t0017g0193a0002c0002t0017g0230 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.54-5031C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910129 | ||||||
chr5:98910208
|
T | C | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-5110A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910208 | ||||||
chr5:98910462
|
G | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-5364C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910462 | ||||||
chr5:98910494
|
G | T | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-5396C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910494 | ||||||
chr5:98910858
|
C | A | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-5760G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910858 | ||||||
chr5:98910930
|
T | C | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.54-5832A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98910930 | ||||||
chr5:98911130
|
G | GA | 16 | a0001c0001t0001g0096a0001c0001t0001g0129a0001c0001t0003g0311others(13): Show | 16 | HG00738.hp1 HG01975.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.54-6033dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911130 | ||||||
chr5:98911130
|
G | GAA | 9 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0113others(6): Show | 9 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.54-6034_54-6033dup others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911130 | ||||||
chr5:98911130
|
GA | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0091others(14): Show | 19 | HG00544.hp2 HG00621.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.54-6033delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911130 | ||||||
chr5:98911130
|
GAA | G | 42 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0090others(39): Show | 43 | HG00408.hp1 HG00438.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.54-6034_54-6033del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911130 | ||||||
chr5:98911142
|
A | AATATATA others(11): Show |
1 | a0001c0001t0001g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.54-6045_54-6044ins others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911142 | ||||||
chr5:98911142
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0250 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.54-6045_54-6044ins others(11): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911142 | ||||||
chr5:98911142
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0015g0040 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.54-6045_54-6044ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911142 | ||||||
chr5:98911142
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0231a0001c0001t0001g0233 | 2 | HG01192.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.54-6045_54-6044ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911142 | ||||||
chr5:98911144
|
A | AATATATA others(13): Show |
2 | a0001c0001t0001g0260a0001c0001t0001g0269 | 2 | HG01070.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | AATATATA others(15): Show |
1 | a0001c0001t0015g0041 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | AT | 3 | a0001c0001t0001g0177a0001c0001t0001g0275a0001c0001t0004g0033 | 3 | HG00544.hp1 HG01099.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(1): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0264 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(26): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0246a0001c0001t0001g0247a0005c0010t0001g0251 | 3 | HG01081.hp1 HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0232a0001c0001t0001g0235a0001c0001t0001g0270others(1): Show | 4 | HG01358.hp2 HG04228.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0298 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0261a0001c0001t0001g0297a0001c0001t0001g0300others(1): Show | 4 | HG02071.hp1 HG02080.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(12): Show |
4 | a0001c0001t0001g0240a0001c0001t0001g0249a0001c0001t0001g0299others(1): Show | 4 | HG02273.hp1 HG02922.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0263 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0239a0001c0001t0001g0258 | 2 | HG01256.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.54-6047_54-6046ins others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0238 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.54-6047_54-6046ins others(25): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
A | T | 13 | a0001c0001t0001g0147a0001c0001t0001g0220a0001c0001t0001g0231others(10): Show | 13 | HG01167.hp1 HG01192.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.54-6046T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911144
|
AAAATATA others(3): Show |
A | 1 | a0001c0001t0001g0280 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.54-6056_54-6047del others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911144 | ||||||
chr5:98911146
|
A | AAAAAAAA others(9): Show |
1 | a0002c0002t0002g0199 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAAAAAA others(19): Show |
1 | a0002c0002t0002g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(26): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAAAAAA others(11): Show |
1 | a0002c0002t0002g0132 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(18): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAAAAAA others(19): Show |
1 | a0002c0002t0011g0076 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(26): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAAAAAA others(23): Show |
1 | a0002c0002t0025g0133 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(30): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAAAAAT others(12): Show |
1 | a0002c0002t0002g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAAAAAT others(26): Show |
1 | a0002c0002t0011g0075 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(33): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAAATAT others(28): Show |
1 | a0002c0002t0011g0073 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(35): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAATATA others(3): Show |
1 | a0001c0003t0006g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAATATA others(15): Show |
2 | a0001c0003t0006g0055a0001c0003t0006g0064 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAATATA others(17): Show |
2 | a0001c0003t0006g0061a0002c0002t0002g0081 | 2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(24): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAATATA others(23): Show |
2 | a0002c0002t0002g0080a0002c0002t0002g0082 | 2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(30): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAATATA others(27): Show |
3 | a0001c0003t0009g0190a0001c0003t0009g0224a0002c0002t0002g0083 | 3 | HG03209.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(34): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAAATATA others(68): Show |
1 | a0002c0002t0002g0074 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(75): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAATATAT others(4): Show |
2 | a0001c0001t0026g0254a0002c0002t0016g0135 | 2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(11): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAATATAT others(8): Show |
1 | a0002c0002t0005g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAATATAT others(10): Show |
2 | a0001c0001t0001g0271a0002c0002t0016g0134 | 2 | HG03540.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAATATAT others(12): Show |
1 | a0001c0001t0001g0241 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAATATAT others(14): Show |
1 | a0001c0001t0001g0289 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAATATAT others(16): Show |
1 | a0002c0002t0005g0022 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AAT | 11 | a0001c0001t0001g0201a0001c0001t0004g0034a0002c0002t0002g0102others(8): Show | 12 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.54-6050_54-6049dup others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AATAT | 7 | a0001c0001t0004g0025a0002c0002t0002g0003a0002c0002t0002g0100others(4): Show | 8 | HG01257.hp1 NA18944.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.54-6052_54-6049dup others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AATATATA others(3): Show |
1 | a0001c0003t0006g0062 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.54-6058_54-6049dup others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AATATATA others(5): Show |
3 | a0001c0001t0001g0253a0001c0001t0001g0255a0001c0003t0006g0053 | 3 | HG01891.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.54-6060_54-6049dup others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AATATATA others(21): Show |
2 | a0002c0002t0002g0079a0002c0002t0005g0023 | 2 | HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.54-6076_54-6049dup others(28): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | AT | 4 | a0001c0001t0001g0153a0001c0001t0003g0306a0002c0002t0002g0110others(1): Show | 4 | HG01069.hp1 HG01169.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(1): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATAT | 9 | a0001c0001t0003g0314a0001c0001t0003g0315a0001c0001t0003g0316others(6): Show | 9 | HG00621.hp2 HG02027.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(3): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATAT | 6 | a0001c0001t0001g0248a0001c0001t0001g0256a0001c0001t0003g0307others(3): Show | 6 | HG01109.hp2 HG01516.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(4): Show |
5 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0286others(2): Show | 5 | HG00423.hp2 HG02015.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(11): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0236a0001c0001t0001g0252 | 2 | HG01257.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(8): Show |
6 | a0001c0001t0001g0044a0001c0001t0001g0284a0001c0001t0001g0285others(3): Show | 6 | HG01928.hp1 HG03139.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(10): Show |
5 | a0001c0001t0001g0234a0001c0001t0001g0259a0001c0001t0001g0291others(2): Show | 5 | HG00642.hp2 HG03490.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0237 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0290a0001c0003t0009g0191 | 2 | HG00323.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0245a0001c0001t0001g0274 | 2 | NA19005.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0001g0283a0001c0003t0006g0063 | 2 | HG01109.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(25): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0244 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(27): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0001g0282 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(29): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATATATAT others(24): Show |
1 | a0001c0003t0006g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(31): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATCTATAT others(16): Show |
1 | a0002c0002t0007g0009 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(23): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATCTATAT others(18): Show |
3 | a0002c0002t0007g0010a0002c0002t0007g0011a0002c0002t0018g0012 | 3 | NA18947.hp2 NA18950.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.54-6049_54-6048ins others(25): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | ATCTATAT others(32): Show |
1 | a0002c0002t0007g0008 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.54-6049_54-6048ins others(39): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
A | T | 72 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0071others(69): Show | 72 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.54-6048T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
AAT | A | 20 | a0001c0001t0001g0089a0001c0001t0001g0097a0001c0001t0001g0139others(17): Show | 20 | HG00408.hp2 HG01346.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.54-6050_54-6049del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911146
|
AATAT | A | 7 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(4): Show | 8 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.54-6052_54-6049del others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911146 | ||||||
chr5:98911147
|
AT | A | 7 | a0001c0001t0001g0099a0001c0001t0001g0173a0001c0001t0004g0024others(4): Show | 7 | HG01243.hp1 HG01255.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.54-6050delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911147 | ||||||
chr5:98911148
|
T | A | 10 | a0001c0001t0003g0313a0001c0004t0001g0087a0001c0004t0001g0088others(7): Show | 10 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.54-6050A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911148 | ||||||
chr5:98911150
|
T | A | 4 | a0001c0001t0001g0176a0001c0001t0001g0182a0001c0001t0001g0217others(1): Show | 4 | HG01346.hp2 HG02257.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-6052A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911150 | ||||||
chr5:98911152
|
T | A | 2 | a0001c0005t0001g0042a0003c0009t0002g0078 | 2 | NA18906.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.54-6054A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911152 | ||||||
chr5:98911154
|
T | A | 2 | a0001c0005t0001g0042a0003c0009t0002g0078 | 2 | NA18906.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.54-6056A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911154 | ||||||
chr5:98911168
|
T | C | 2 | a0002c0002t0005g0014a0002c0002t0005g0015 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.54-6070A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911168 | ||||||
chr5:98911176
|
T | G | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-6078A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911176 | ||||||
chr5:98911219
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.54-6121T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911219 | ||||||
chr5:98911287
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.54-6189A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911287 | ||||||
chr5:98911337
|
A | T | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.54-6239T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911337 | ||||||
chr5:98911484
|
T | C | 72 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(69): Show | 72 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.54-6386A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911484 | ||||||
chr5:98911518
|
G | A | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-6420C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911518 | ||||||
chr5:98911725
|
G | T | 1 | a0001c0001t0003g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.54-6627C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911725 | ||||||
chr5:98911983
|
C | A | 1 | a0001c0001t0001g0174 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.54-6885G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98911983 | ||||||
chr5:98912340
|
A | T | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.54-7242T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912340 | ||||||
chr5:98912548
|
G | A | 70 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(67): Show | 72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.54-7450C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912548 | ||||||
chr5:98912578
|
C | T | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.54-7480G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912578 | ||||||
chr5:98912649
|
C | T | 1 | a0001c0001t0003g0315 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.54-7551G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912649 | ||||||
chr5:98912680
|
A | G | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-7582T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912680 | ||||||
chr5:98912730
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.54-7632G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98912730 | ||||||
chr5:98913201
|
T | C | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-8103A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913201 | ||||||
chr5:98913680
|
T | C | 3 | a0001c0003t0009g0190a0001c0003t0009g0224a0002c0002t0005g0021 | 3 | HG02976.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.54-8582A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913680 | ||||||
chr5:98913717
|
A | G | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.54-8619T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913717 | ||||||
chr5:98913740
|
G | T | 10 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0110others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.54-8642C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913740 | ||||||
chr5:98913780
|
TAATACA | T | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.54-8688_54-8683del others(6): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913780 | ||||||
chr5:98913851
|
G | A | 105 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0003t0002g0002others(102): Show | 109 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.54-8753C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913851 | ||||||
chr5:98913909
|
T | C | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.54-8811A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913909 | ||||||
chr5:98913933
|
T | A | 18 | a0001c0001t0001g0140a0001c0001t0001g0202a0001c0001t0001g0203others(15): Show | 18 | HG00741.hp2 HG01099.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.54-8835A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913933 | ||||||
chr5:98913934
|
A | T | 10 | a0001c0001t0001g0145a0001c0003t0002g0002a0001c0003t0002g0056others(7): Show | 11 | HG00323.hp1 HG01891.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.54-8836T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98913934 | ||||||
chr5:98914029
|
G | A | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-8931C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914029 | ||||||
chr5:98914244
|
G | C | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.54-9146C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914244 | ||||||
chr5:98914305
|
G | T | 2 | a0002c0002t0017g0193a0002c0002t0017g0230 | 2 | HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.54-9207C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914305 | ||||||
chr5:98914517
|
G | GA | 36 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(33): Show | 38 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.54-9420dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914517 | ||||||
chr5:98914649
|
C | T | 1 | a0001c0003t0006g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.54-9551G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914649 | ||||||
chr5:98914838
|
C | G | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.54-9740G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914838 | ||||||
chr5:98914887
|
A | ATC | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.54-9791_54-9790dup others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98914887 | ||||||
chr5:98915101
|
C | T | 49 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0090others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.54-10003G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915101 | ||||||
chr5:98915154
|
T | C | 34 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(31): Show | 34 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.54-10056A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915154 | ||||||
chr5:98915406
|
A | AGGAAGAG others(334): Show |
1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54-10309_54-10308i others(343): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915406 | ||||||
chr5:98915496
|
T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.54-10398A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915496 | ||||||
chr5:98915601
|
A | G | 13 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(10): Show | 13 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.54-10503T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915601 | ||||||
chr5:98915870
|
A | G | 4 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(1): Show | 4 | HG01496.hp2 HG02572.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+10464T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98915870 | ||||||
chr5:98916035
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.53+10299T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916035 | ||||||
chr5:98916073
|
T | C | 3 | a0002c0002t0002g0108a0002c0002t0002g0109a0002c0002t0002g0117 | 3 | HG00642.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.53+10261A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916073 | ||||||
chr5:98916106
|
C | T | 3 | a0002c0002t0002g0102a0002c0002t0002g0118a0002c0002t0002g0192 | 3 | NA18965.hp2 NA18981.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.53+10228G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916106 | ||||||
chr5:98916284
|
A | G | 106 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0003g0307others(103): Show | 110 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(107): Show |
intron_variant | MODIFIER | c.53+10050T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916284 | ||||||
chr5:98916344
|
G | A | 4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0263others(1): Show | 4 | HG01243.hp2 NA18987.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+9990C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916344 | ||||||
chr5:98916442
|
G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0214 | 3 | HG01943.hp2 NA19056.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.53+9892C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916442 | ||||||
chr5:98916470
|
G | A | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53+9864C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916470 | ||||||
chr5:98916491
|
G | C | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+9843C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916491 | ||||||
chr5:98916545
|
C | CA | 42 | a0001c0001t0001g0138a0001c0001t0001g0177a0001c0001t0001g0178others(39): Show | 42 | HG00423.hp2 HG01109.hp2 HG01257.hp2 others(39): Show |
intron_variant | MODIFIER | c.53+9788dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916545 | ||||||
chr5:98916545
|
CA | C | 12 | a0001c0001t0001g0084a0001c0001t0001g0142a0001c0001t0001g0200others(9): Show | 12 | HG00323.hp2 HG00642.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+9788delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916545 | ||||||
chr5:98916545
|
CAA | C | 25 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(22): Show | 27 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.53+9787_53+9788del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916545 | ||||||
chr5:98916571
|
G | C | 72 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(69): Show | 72 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.53+9763C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916571 | ||||||
chr5:98916784
|
T | C | 33 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(30): Show | 35 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.53+9550A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916784 | ||||||
chr5:98916791
|
T | C | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.53+9543A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916791 | ||||||
chr5:98916928
|
C | CAT | 72 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(69): Show | 72 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.53+9405_53+9406ins others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916928 | ||||||
chr5:98916929
|
G | A | 228 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.53+9405C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98916929 | ||||||
chr5:98917202
|
T | C | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+9132A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917202 | ||||||
chr5:98917299
|
C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0084a0001c0001t0001g0089a0001c0001t0001g0288others(2): Show | 5 | HG01884.hp1 HG02074.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CAAAAAAA others(7): Show |
93 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0091others(90): Show | 93 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CAAAAAAA others(8): Show |
22 | a0001c0001t0001g0097a0001c0001t0001g0235a0001c0001t0001g0249others(19): Show | 22 | HG00423.hp1 HG01081.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(15): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0281 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(16): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA | 29 | a0002c0002t0002g0074a0002c0002t0002g0077a0002c0002t0002g0079others(26): Show | 29 | HG00323.hp1 HG01167.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(7): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(1): Show |
30 | a0002c0002t0002g0100a0002c0002t0002g0101a0002c0002t0002g0108others(27): Show | 31 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(8): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(3): Show |
8 | a0002c0002t0002g0003a0002c0002t0002g0102a0002c0002t0002g0103others(5): Show | 9 | NA18944.hp1 NA18946.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(10): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(4): Show |
1 | a0002c0002t0002g0107 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(11): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(5): Show |
3 | a0001c0003t0005g0017a0001c0003t0009g0190a0001c0003t0009g0224 | 3 | HG02622.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(12): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(6): Show |
2 | a0001c0003t0009g0191a0001c0003t0009g0225 | 2 | HG00323.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(13): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(7): Show |
4 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0003t0002g0227others(1): Show | 4 | HG00741.hp1 HG01243.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(14): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(10): Show |
2 | a0001c0003t0002g0056a0001c0003t0002g0057 | 2 | HG01891.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(17): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(12): Show |
1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(19): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(13): Show |
5 | a0001c0003t0006g0052a0001c0003t0006g0053a0001c0003t0006g0054others(2): Show | 5 | HG02258.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(20): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(14): Show |
2 | a0001c0003t0006g0063a0001c0003t0006g0064 | 2 | HG01109.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(21): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(15): Show |
2 | a0001c0003t0006g0055a0001c0003t0006g0066 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(22): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(18): Show |
1 | a0001c0003t0002g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(25): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(19): Show |
1 | a0001c0003t0020g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.53+9034_53+9035ins others(26): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(20): Show |
4 | a0001c0003t0002g0058a0001c0003t0002g0059a0001c0003t0013g0007others(1): Show | 5 | HG06807.hp1 NA19030.hp2 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(27): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(21): Show |
5 | a0001c0003t0002g0002a0001c0003t0002g0065a0001c0003t0012g0301others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(28): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917299
|
C | CCAAAAAA others(22): Show |
3 | a0001c0003t0002g0049a0001c0003t0002g0050a0001c0003t0002g0060 | 3 | HG02896.hp2 HG02897.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.53+9034_53+9035ins others(29): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917299 | ||||||
chr5:98917312
|
C | A | 5 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(2): Show | 5 | HG00323.hp2 HG02886.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+9022G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917312 | ||||||
chr5:98917313
|
A | C | 70 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(67): Show | 72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+9021T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917313 | ||||||
chr5:98917372
|
T | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.53+8962A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917372 | ||||||
chr5:98917377
|
T | C | 2 | a0001c0005t0001g0042a0001c0005t0022g0043 | 2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.53+8957A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917377 | ||||||
chr5:98917451
|
A | G | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+8883T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917451 | ||||||
chr5:98917498
|
C | T | 2 | a0001c0003t0013g0007a0001c0003t0013g0303 | 3 | HG06807.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.53+8836G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917498 | ||||||
chr5:98917816
|
A | G | 1 | a0002c0002t0002g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.53+8518T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917816 | ||||||
chr5:98917937
|
T | C | 13 | a0002c0002t0005g0014a0002c0002t0005g0015a0002c0002t0005g0016others(10): Show | 13 | HG02055.hp2 HG02258.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.53+8397A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98917937 | ||||||
chr5:98918060
|
CT | C | 105 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0235others(102): Show | 109 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.53+8273delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918060 | ||||||
chr5:98918127
|
G | A | 2 | a0002c0002t0005g0022a0002c0002t0005g0023 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.53+8207C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918127 | ||||||
chr5:98918136
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0205 | 2 | NA19058.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.53+8198G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918136 | ||||||
chr5:98918206
|
C | T | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+8128G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918206 | ||||||
chr5:98918438
|
C | T | 3 | a0001c0001t0001g0189a0001c0001t0001g0200a0001c0001t0003g0312 | 3 | HG02004.hp2 HG02273.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.53+7896G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918438 | ||||||
chr5:98918460
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.53+7874C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918460 | ||||||
chr5:98918536
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.53+7798T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918536 | ||||||
chr5:98918540
|
C | T | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.53+7794G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918540 | ||||||
chr5:98918604
|
C | G | 2 | a0001c0001t0001g0204a0001c0001t0019g0013 | 2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.53+7730G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918604 | ||||||
chr5:98918638
|
C | T | 1 | a0001c0001t0001g0232 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.53+7696G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918638 | ||||||
chr5:98918673
|
C | G | 5 | a0001c0003t0012g0301a0001c0003t0012g0302a0001c0003t0012g0304others(2): Show | 6 | HG02486.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+7661G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918673 | ||||||
chr5:98918693
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.53+7641C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918693 | ||||||
chr5:98918767
|
AAC | A | 7 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017others(4): Show | 7 | HG00323.hp2 HG00741.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.53+7565_53+7566del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918767 | ||||||
chr5:98918769
|
C | A | 32 | a0001c0001t0015g0040a0001c0003t0002g0002a0001c0003t0002g0048others(29): Show | 34 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.53+7565G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918769 | ||||||
chr5:98918769
|
CA | C | 64 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(61): Show | 66 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.53+7564delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918769 | ||||||
chr5:98918770
|
A | C | 36 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(33): Show | 38 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.53+7564T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918770 | ||||||
chr5:98918850
|
A | G | 3 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199 | 3 | HG02572.hp1 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.53+7484T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98918850 | ||||||
chr5:98919096
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.53+7238A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919096 | ||||||
chr5:98919202
|
G | C | 8 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(5): Show | 9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+7132C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919202 | ||||||
chr5:98919225
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.53+7109C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919225 | ||||||
chr5:98919490
|
T | G | 5 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(2): Show | 5 | HG01981.hp2 NA18949.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+6844A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919490 | ||||||
chr5:98919709
|
C | G | 3 | a0001c0001t0003g0309a0001c0001t0003g0310a0001c0001t0003g0311 | 3 | HG01975.hp1 HG01993.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.53+6625G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919709 | ||||||
chr5:98919751
|
A | G | 6 | a0002c0002t0002g0131a0002c0002t0002g0132a0002c0002t0002g0199others(3): Show | 6 | HG01496.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.53+6583T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919751 | ||||||
chr5:98919781
|
G | A | 1 | a0001c0001t0030g0327 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.53+6553C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919781 | ||||||
chr5:98919865
|
A | G | 1 | a0002c0002t0002g0072 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.53+6469T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919865 | ||||||
chr5:98919906
|
T | C | 1 | a0002c0002t0005g0021 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.53+6428A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919906 | ||||||
chr5:98919922
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.53+6412T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98919922 | ||||||
chr5:98920111
|
A | G | 2 | a0001c0001t0003g0321a0001c0001t0014g0324 | 2 | HG02027.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.53+6223T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920111 | ||||||
chr5:98920142
|
G | A | 3 | a0002c0002t0010g0004a0002c0002t0010g0121a0002c0002t0010g0122 | 4 | NA18949.hp2 NA18970.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+6192C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920142 | ||||||
chr5:98920175
|
C | T | 9 | a0002c0002t0002g0003a0002c0002t0002g0102a0002c0002t0002g0103others(6): Show | 10 | NA18944.hp1 NA18946.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.53+6159G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920175 | ||||||
chr5:98920273
|
C | A | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+6061G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920273 | ||||||
chr5:98920392
|
A | C | 3 | a0001c0001t0001g0140a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG01099.hp2 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.53+5942T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920392 | ||||||
chr5:98920433
|
G | T | 70 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(67): Show | 72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+5901C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920433 | ||||||
chr5:98920535
|
A | G | 1 | a0002c0002t0002g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.53+5799T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920535 | ||||||
chr5:98920586
|
C | T | 2 | a0001c0003t0009g0190a0001c0003t0009g0224 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53+5748G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920586 | ||||||
chr5:98920675
|
T | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01256.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.53+5659A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920675 | ||||||
chr5:98920752
|
G | A | 8 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(5): Show | 9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+5582C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920752 | ||||||
chr5:98920789
|
G | A | 6 | a0001c0004t0001g0085a0001c0004t0001g0086a0001c0004t0001g0087others(3): Show | 6 | HG02723.hp1 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.53+5545C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920789 | ||||||
chr5:98920792
|
G | A | 1 | a0001c0001t0004g0036 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.53+5542C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920792 | ||||||
chr5:98920796
|
C | CA | 13 | a0001c0001t0001g0187a0001c0001t0001g0264a0001c0001t0001g0282others(10): Show | 13 | HG00741.hp1 HG01496.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.53+5537dupT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920796 | ||||||
chr5:98920796
|
CA | C | 14 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0262others(11): Show | 14 | HG01109.hp1 HG01168.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.53+5537delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920796 | ||||||
chr5:98920812
|
A | G | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.53+5522T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920812 | ||||||
chr5:98920820
|
T | A | 1 | a0001c0003t0005g0017 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.53+5514A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920820 | ||||||
chr5:98920833
|
A | G | 103 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(100): Show | 107 | HG00323.hp1 HG00323.hp2 HG00642.hp1 others(104): Show |
intron_variant | MODIFIER | c.53+5501T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98920833 | ||||||
chr5:98921028
|
G | A | 1 | a0002c0002t0002g0119 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.53+5306C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921028 | ||||||
chr5:98921084
|
CTT | C | 12 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050others(9): Show | 12 | HG01109.hp1 HG01884.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.53+5248_53+5249del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921084 | ||||||
chr5:98921126
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.53+5208G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921126 | ||||||
chr5:98921171
|
G | A | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.53+5163C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921171 | ||||||
chr5:98921201
|
T | C | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.53+5133A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921201 | ||||||
chr5:98921252
|
G | A | 9 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(6): Show | 9 | HG00642.hp2 HG01070.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+5082C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921252 | ||||||
chr5:98921462
|
C | T | 3 | a0001c0001t0003g0305a0001c0001t0003g0306a0001c0001t0003g0307 | 3 | HG01515.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.53+4872G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921462 | ||||||
chr5:98921492
|
T | A | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.53+4842A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921492 | ||||||
chr5:98921665
|
A | C | 99 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(96): Show | 103 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.53+4669T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921665 | ||||||
chr5:98921670
|
G | A | 1 | a0001c0001t0004g0032 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.53+4664C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921670 | ||||||
chr5:98921737
|
C | T | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.53+4597G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921737 | ||||||
chr5:98921812
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0221 | 2 | NA18946.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.53+4522A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921812 | ||||||
chr5:98921907
|
T | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+4427A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921907 | ||||||
chr5:98921979
|
C | G | 5 | a0001c0004t0001g0085a0001c0004t0001g0086a0001c0004t0001g0087others(2): Show | 5 | HG03041.hp1 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+4355G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98921979 | ||||||
chr5:98922017
|
G | C | 3 | a0001c0001t0001g0262a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | NA18948.hp1 NA18987.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.53+4317C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922017 | ||||||
chr5:98922071
|
G | T | 1 | a0002c0002t0005g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53+4263C>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922071 | ||||||
chr5:98922146
|
T | C | 34 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(31): Show | 34 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.53+4188A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922146 | ||||||
chr5:98922214
|
T | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+4120A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922214 | ||||||
chr5:98922295
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.53+4039T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922295 | ||||||
chr5:98922331
|
T | C | 3 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0267 | 3 | HG02818.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.53+4003A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922331 | ||||||
chr5:98922407
|
A | C | 1 | a0001c0001t0001g0236 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.53+3927T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922407 | ||||||
chr5:98922475
|
T | C | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+3859A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922475 | ||||||
chr5:98922481
|
A | T | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.53+3853T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922481 | ||||||
chr5:98922783
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.53+3551C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922783 | ||||||
chr5:98922811
|
A | G | 1 | a0001c0003t0028g0051 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53+3523T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922811 | ||||||
chr5:98922844
|
C | G | 2 | a0002c0002t0007g0008a0002c0002t0007g0010 | 2 | NA18955.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.53+3490G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922844 | ||||||
chr5:98922920
|
C | T | 1 | a0001c0001t0004g0024 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.53+3414G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922920 | ||||||
chr5:98922976
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.53+3358T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922976 | ||||||
chr5:98922996
|
AG | A | 35 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(32): Show | 35 | HG00323.hp1 HG01243.hp1 HG01358.hp1 others(32): Show |
intron_variant | MODIFIER | c.53+3337delC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98922996 | ||||||
chr5:98923032
|
T | C | 1 | a0002c0002t0002g0194 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.53+3302A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923032 | ||||||
chr5:98923039
|
T | G | 2 | a0002c0002t0002g0120a0002c0002t0002g0195 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.53+3295A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923039 | ||||||
chr5:98923042
|
A | G | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+3292T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923042 | ||||||
chr5:98923070
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.53+3264G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923070 | ||||||
chr5:98923229
|
G | A | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.53+3105C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923229 | ||||||
chr5:98923234
|
C | G | 1 | a0001c0005t0001g0042 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.53+3100G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923234 | ||||||
chr5:98923380
|
T | C | 3 | a0002c0002t0010g0004a0002c0002t0010g0121a0002c0002t0010g0122 | 4 | NA18949.hp2 NA18970.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.53+2954A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923380 | ||||||
chr5:98923408
|
G | A | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+2926C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923408 | ||||||
chr5:98923418
|
AT | A | 8 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0268others(5): Show | 8 | HG00323.hp2 HG01243.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.53+2915delA | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923418 | ||||||
chr5:98923418
|
ATT | A | 98 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(95): Show | 102 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.53+2914_53+2915del others(2): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923418 | ||||||
chr5:98923451
|
T | C | 2 | a0001c0005t0001g0042a0001c0005t0022g0043 | 2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.53+2883A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923451 | ||||||
chr5:98923480
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.53+2854T>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923480 | ||||||
chr5:98923543
|
C | T | 1 | a0002c0002t0002g0100 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.53+2791G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923543 | ||||||
chr5:98923693
|
G | A | 70 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(67): Show | 72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+2641C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923693 | ||||||
chr5:98923909
|
T | C | 7 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(4): Show | 8 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.53+2425A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923909 | ||||||
chr5:98923969
|
T | G | 8 | a0001c0003t0002g0002a0001c0003t0002g0056a0001c0003t0002g0057others(5): Show | 9 | HG01891.hp2 HG02886.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.53+2365A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98923969 | ||||||
chr5:98924090
|
T | C | 5 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017others(2): Show | 5 | HG00741.hp1 HG01255.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.53+2244A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924090 | ||||||
chr5:98924118
|
T | C | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.53+2216A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924118 | ||||||
chr5:98924143
|
G | C | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.53+2191C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924143 | ||||||
chr5:98924254
|
A | T | 1 | a0001c0001t0001g0138 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.53+2080T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924254 | ||||||
chr5:98924383
|
C | G | 1 | a0002c0002t0007g0008 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.53+1951G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924383 | ||||||
chr5:98924533
|
G | A | 70 | a0002c0002t0002g0003a0002c0002t0002g0072a0002c0002t0002g0074others(67): Show | 72 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.53+1801C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924533 | ||||||
chr5:98924578
|
C | G | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+1756G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924578 | ||||||
chr5:98924588
|
C | T | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.53+1746G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924588 | ||||||
chr5:98924774
|
G | A | 16 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(13): Show | 16 | HG00423.hp2 HG02015.hp2 NA18951.hp1 others(13): Show |
intron_variant | MODIFIER | c.53+1560C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924774 | ||||||
chr5:98924823
|
C | G | 3 | a0001c0003t0012g0301a0001c0003t0012g0302a0001c0003t0012g0304 | 3 | HG02486.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.53+1511G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924823 | ||||||
chr5:98924851
|
G | A | 2 | a0001c0003t0002g0227a0001c0003t0002g0228 | 2 | HG00741.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+1483C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924851 | ||||||
chr5:98924851
|
G | C | 1 | a0002c0002t0005g0023 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.53+1483C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924851 | ||||||
chr5:98924871
|
C | T | 1 | a0001c0001t0027g0137 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.53+1463G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924871 | ||||||
chr5:98924872
|
G | A | 3 | a0001c0003t0002g0227a0001c0003t0002g0228a0001c0003t0005g0017 | 3 | HG00741.hp1 HG02622.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.53+1462C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924872 | ||||||
chr5:98924885
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.53+1449C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924885 | ||||||
chr5:98924945
|
T | A | 1 | a0001c0001t0003g0321 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53+1389A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924945 | ||||||
chr5:98924947
|
C | T | 5 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(2): Show | 5 | HG01099.hp1 HG01192.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.53+1387G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98924947 | ||||||
chr5:98925017
|
C | A | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+1317G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925017 | ||||||
chr5:98925258
|
T | C | 2 | a0001c0001t0014g0324a0001c0001t0014g0325 | 2 | NA18983.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.53+1076A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925258 | ||||||
chr5:98925281
|
C | G | 228 | a0001c0001t0001g0044a0001c0001t0001g0070a0001c0001t0001g0071others(225): Show | 232 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.53+1053G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925281 | ||||||
chr5:98925327
|
G | C | 2 | a0002c0002t0002g0125a0002c0002t0002g0126 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.53+1007C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925327 | ||||||
chr5:98925687
|
C | A | 1 | a0001c0001t0001g0222 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.53+647G>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925687 | ||||||
chr5:98925705
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.53+629T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925705 | ||||||
chr5:98925782
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.53+552A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98925782 | ||||||
chr5:98926104
|
T | G | 1 | a0001c0001t0001g0223 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53+230A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98926104 | ||||||
chr5:98926108
|
T | C | 4 | a0001c0003t0009g0190a0001c0003t0009g0191a0001c0003t0009g0224others(1): Show | 4 | HG00323.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.53+226A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98926108 | ||||||
chr5:98926187
|
T | C | 35 | a0002c0002t0002g0003a0002c0002t0002g0100a0002c0002t0002g0101others(32): Show | 37 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.53+147A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 2/35 | chr5 | 98926187 | ||||||
chr5:98926596
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-148-62A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926596 | ||||||
chr5:98926918
|
T | TG | 59 | a0001c0001t0001g0044a0001c0001t0001g0047a0001c0001t0001g0067others(56): Show | 59 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.-148-385dupC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926918 | ||||||
chr5:98926918
|
T | TGG | 19 | a0001c0001t0001g0229a0001c0001t0001g0289a0001c0001t0001g0290others(16): Show | 19 | HG00423.hp2 HG00741.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-148-386_-148-385d others(4): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926918 | ||||||
chr5:98926918
|
TG | T | 77 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0084others(74): Show | 79 | HG00423.hp1 HG00544.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-148-385delC | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926918 | ||||||
chr5:98926943
|
C | CCTT | 3 | a0001c0003t0002g0048a0001c0003t0002g0049a0001c0003t0002g0050 | 3 | HG02896.hp2 HG02897.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-148-412_-148-410d others(5): Show |
CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926943 | ||||||
chr5:98926989
|
G | A | 1 | a0001c0001t0004g0036 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-148-455C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98926989 | ||||||
chr5:98927105
|
T | C | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-148-571A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927105 | ||||||
chr5:98927212
|
C | T | 12 | a0002c0002t0002g0072a0002c0002t0002g0074a0002c0002t0002g0077others(9): Show | 12 | HG00323.hp1 HG01358.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.-148-678G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927212 | ||||||
chr5:98927333
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-148-799G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927333 | ||||||
chr5:98927409
|
T | A | 1 | a0001c0001t0001g0294 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-148-875A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927409 | ||||||
chr5:98927595
|
T | A | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-149+944A>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927595 | ||||||
chr5:98927629
|
A | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01243.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-149+910T>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927629 | ||||||
chr5:98927725
|
TA | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0006t0001g0069 | 3 | HG02083.hp2 NA18998.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-149+813delT | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927725 | ||||||
chr5:98927865
|
T | G | 72 | a0001c0001t0001g0044a0001c0001t0001g0231a0001c0001t0001g0232others(69): Show | 72 | HG00423.hp2 HG00642.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.-149+674A>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927865 | ||||||
chr5:98927901
|
C | T | 26 | a0001c0003t0002g0002a0001c0003t0002g0048a0001c0003t0002g0049others(23): Show | 28 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-149+638G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927901 | ||||||
chr5:98927982
|
G | C | 2 | a0002c0002t0002g0295a0002c0002t0005g0021 | 2 | HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-149+557C>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98927982 | ||||||
chr5:98928034
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-149+505A>G | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928034 | ||||||
chr5:98928084
|
C | T | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | NA18969.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-149+455G>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928084 | ||||||
chr5:98928200
|
C | G | 1 | a0002c0002t0024g0045 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-149+339G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928200 | ||||||
chr5:98928201
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-149+338G>C | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928201 | ||||||
chr5:98928291
|
A | T | 2 | a0001c0005t0001g0042a0001c0005t0022g0043 | 2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-149+248T>A | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928291 | ||||||
chr5:98928325
|
G | A | 2 | a0002c0002t0005g0022a0002c0002t0005g0023 | 2 | HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-149+214C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928325 | ||||||
chr5:98928399
|
G | A | 4 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(1): Show | 4 | HG02071.hp1 HG02080.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-149+140C>T | CHD1 | ENSG00000153922.12 | transcript | ENST00000614616.5 | protein_coding | 1/35 | chr5 | 98928399 |