geneid | 79869 |
---|---|
ensemblid | ENSG00000149532.16 |
hgncid | 30098 |
symbol | CPSF7 |
name | cleavage and polyadenylation specific factor 7 |
refseq_nuc | NM_001142565.3 |
refseq_prot | NP_001136037.1 |
ensembl_nuc | ENST00000439958.8 |
ensembl_prot | ENSP00000397203.3 |
mane_status | MANE Select |
chr | chr11 |
start | 61402729 |
end | 61429975 |
strand | - |
ver | v1.2 |
region | chr11:61402729-61429975 |
region5000 | chr11:61397729-61434975 |
regionname0 | CPSF7_chr11_61402729_61429975 |
regionname5000 | CPSF7_chr11_61397729_61434975 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 462 | 190 | 88 | 40 | 28 | 6 | 26 | 14 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2099 | 152 | 58 | 38 | 22 | 6 | 26 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
t0002 | 0/0 | 2098 | 18 | 16 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
t0003 | 0/0 | 2097 | 9 | 9 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
t0004 | 0/0 | 2099 | 5 | 5 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
t0005 | 0/0 | 2099 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
t0006 | 0/0 | 2099 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
t0007 | 0/0 | 2099 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
t0008 | 0/0 | 2099 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/1 | 11 | 1 | 3 | 2 | 1 | 3 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0002 | 0/0 | 7 | 2 | 1 | 1 | 1 | 2 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0004 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1389 | 97 | 71 | 11 | 5 | 2 | 7 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0002 | 0/1 | 1389 | 93 | 17 | 29 | 23 | 4 | 19 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3487 | 65 | 41 | 9 | 5 | 2 | 7 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0001t0002 | 0/0 | 3486 | 18 | 16 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0001t0003 | 0/0 | 3485 | 9 | 9 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0001t0004 | 0/0 | 3487 | 5 | 5 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0002t0001 | 0/1 | 3487 | 87 | 17 | 29 | 17 | 4 | 19 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0002t0005 | 0/0 | 3487 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0002t0006 | 0/0 | 3487 | 2 | 0 | 0 | 2 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0002t0007 | 0/0 | 3487 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
a0001c0002t0008 | 0/0 | 3487 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | copy fasta | chr11 | 61397729 | 61434975 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0028 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0003g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0001 | 0/1 | 11 | 1 | 3 | 2 | 1 | 3 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0002 | 0/0 | 7 | 2 | 1 | 1 | 1 | 2 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0003 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
a0001c0002t0008g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0056 | EUR | GBR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00673 | hp1 | a0001 | c0002 | t0007 | g0016 | EAS | CHS | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00673 | hp2 | a0001 | c0002 | t0008 | g0100 | EAS | CHS | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0063 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0055 | EUR | IBS | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02083 | hp2 | a0001 | c0002 | t0006 | g0077 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0068 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | KHV | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | CDX | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0064 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0095 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0067 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ESN | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0059 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0105 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | STU | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | STU | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0058 | SAS | STU | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19001 | hp1 | a0001 | c0002 | t0006 | g0108 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19075 | hp2 | a0001 | c0002 | t0005 | g0089 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | YRI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ASW | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ASW | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | TSI | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | GIH | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ACB | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | USA | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0001 | REF | REF | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0028 | REF | REF | CPSF7_chr11_61397729_61434975 | CPSF7 | chr11 | 61397729 | 61434975 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61411813
|
G | A | 1 | a0001c0002 | 93 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
synonymous_variant | LOW | c.1182C>T | p.Ile394Ile | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/10 | 1299/3487 | 1182/1389 | 394/462 | chr11 | 61411813 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61402920
|
G | A | 1 | a0001c0002t0005 | 2 | HG02129.hp2 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1790C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 8023 | chr11 | 61402920 | |||||
chr11:61402969
|
AC | A | 2 | a0001c0001t0002a0001c0001t0003 | 27 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1740delG | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 7973 | chr11 | 61402969 | |||||
chr11:61404398
|
C | T | 1 | a0001c0002t0008 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 6545 | chr11 | 61404398 | |||||
chr11:61404444
|
G | A | 1 | a0001c0002t0006 | 2 | HG02083.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*266C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 6499 | chr11 | 61404444 | |||||
chr11:61404467
|
AC | A | 1 | a0001c0001t0003 | 9 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*242delG | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 6475 | chr11 | 61404467 | |||||
chr11:61404594
|
G | C | 1 | a0001c0001t0004 | 5 | HG02451.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*116C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 10/10 | 6349 | chr11 | 61404594 | |||||
chr11:61429947
|
C | G | 1 | a0001c0002t0007 | 1 | HG00673.hp1 | 5_prime_UTR_variant | MODIFIER | c.-89G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/10 | 712 | chr11 | 61429947 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61404851
|
CAA | C | 2 | a0001c0001t0003g0116a0001c0001t0003g0141 | 2 | HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.*6-149_*6-148delTT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61404851 | ||||||
chr11:61404860
|
A | C | 1 | a0001c0002t0001g0067 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.*6-156T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61404860 | ||||||
chr11:61405024
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.*6-320T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405024 | ||||||
chr11:61405169
|
C | T | 1 | a0001c0002t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.*6-465G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405169 | ||||||
chr11:61405235
|
CAT | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.*6-533_*6-532delAT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405235 | ||||||
chr11:61405333
|
A | G | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.*6-629T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405333 | ||||||
chr11:61405365
|
T | C | 5 | a0001c0001t0001g0130a0001c0001t0001g0132a0001c0001t0001g0133others(2): Show | 5 | HG02451.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.*6-661A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405365 | ||||||
chr11:61405402
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.*6-698G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405402 | ||||||
chr11:61405864
|
C | T | 113 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 146 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(143): Show |
intron_variant | MODIFIER | c.*6-1160G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61405864 | ||||||
chr11:61406013
|
C | T | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0136others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.*6-1309G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406013 | ||||||
chr11:61406142
|
T | C | 150 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(147): Show | 188 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(185): Show |
intron_variant | MODIFIER | c.*6-1438A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406142 | ||||||
chr11:61406143
|
A | G | 1 | a0001c0002t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.*6-1439T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406143 | ||||||
chr11:61406318
|
G | C | 2 | a0001c0002t0001g0069a0001c0002t0001g0109 | 2 | HG01943.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.*6-1614C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406318 | ||||||
chr11:61406403
|
C | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0036others(1): Show | 5 | HG01081.hp1 HG01978.hp1 HG02015.hp1 others(2): Show |
intron_variant | MODIFIER | c.*6-1699G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406403 | ||||||
chr11:61406667
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*6-1963T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406667 | ||||||
chr11:61406787
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*6-2083C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406787 | ||||||
chr11:61406887
|
C | CT | 3 | a0001c0001t0002g0007a0001c0001t0002g0127a0001c0001t0002g0128 | 5 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.*6-2184dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406887 | ||||||
chr11:61406958
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.*6-2254C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61406958 | ||||||
chr11:61407444
|
C | G | 1 | a0001c0001t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*6-2740G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61407444 | ||||||
chr11:61408057
|
C | CT | 29 | a0001c0001t0001g0015a0001c0001t0001g0111a0001c0001t0001g0112others(26): Show | 35 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.*5+2880dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408057 | ||||||
chr11:61408057
|
C | CTT | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0117others(10): Show | 15 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.*5+2879_*5+2880dup others(2): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408057 | ||||||
chr11:61408149
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.*5+2789G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408149 | ||||||
chr11:61408183
|
A | T | 1 | a0001c0001t0004g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.*5+2755T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408183 | ||||||
chr11:61408229
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0003g0114 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.*5+2709A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408229 | ||||||
chr11:61408353
|
C | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0037a0001c0001t0001g0042 | 3 | HG01109.hp2 HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.*5+2585G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408353 | ||||||
chr11:61408532
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.*5+2406C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408532 | ||||||
chr11:61408637
|
A | C | 21 | a0001c0001t0001g0117a0001c0001t0002g0005a0001c0001t0002g0007others(18): Show | 28 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.*5+2301T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408637 | ||||||
chr11:61408901
|
C | T | 1 | a0001c0002t0001g0073 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.*5+2037G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408901 | ||||||
chr11:61408952
|
G | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0125others(2): Show | 7 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.*5+1986C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61408952 | ||||||
chr11:61409107
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.*5+1831A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409107 | ||||||
chr11:61409148
|
T | G | 4 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | HG02080.hp1 NA18950.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.*5+1790A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409148 | ||||||
chr11:61409167
|
A | C | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 52 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(49): Show |
intron_variant | MODIFIER | c.*5+1771T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409167 | ||||||
chr11:61409194
|
C | A | 1 | a0001c0002t0001g0069 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.*5+1744G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409194 | ||||||
chr11:61409286
|
A | T | 2 | a0001c0002t0001g0062a0001c0002t0001g0063 | 2 | HG01255.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.*5+1652T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409286 | ||||||
chr11:61409328
|
C | T | 11 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0122others(8): Show | 16 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.*5+1610G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409328 | ||||||
chr11:61409333
|
G | A | 70 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(67): Show | 93 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.*5+1605C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409333 | ||||||
chr11:61409664
|
GT | G | 110 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(107): Show | 143 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(140): Show |
intron_variant | MODIFIER | c.*5+1273delA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409664 | ||||||
chr11:61409948
|
C | T | 7 | a0001c0001t0002g0005a0001c0001t0002g0122a0001c0001t0002g0123others(4): Show | 10 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.*5+990G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409948 | ||||||
chr11:61409987
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.*5+951C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61409987 | ||||||
chr11:61410479
|
AATG | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0111others(9): Show | 14 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.*5+456_*5+458delCA others(1): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61410479 | ||||||
chr11:61410554
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0034 | 2 | HG01433.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.*5+384A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 9/9 | chr11 | 61410554 | ||||||
chr11:61411340
|
G | A | 1 | a0001c0001t0001g0020 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1227-235C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/9 | chr11 | 61411340 | ||||||
chr11:61411534
|
T | C | 113 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 146 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(143): Show |
intron_variant | MODIFIER | c.1226+235A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/9 | chr11 | 61411534 | ||||||
chr11:61411537
|
G | C | 1 | a0001c0002t0001g0091 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1226+232C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/9 | chr11 | 61411537 | ||||||
chr11:61411555
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1226+214T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 8/9 | chr11 | 61411555 | ||||||
chr11:61412256
|
G | A | 70 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(67): Show | 93 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.1058-319C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412256 | ||||||
chr11:61412359
|
G | A | 6 | a0001c0001t0002g0007a0001c0001t0002g0127a0001c0001t0002g0128others(3): Show | 8 | HG02280.hp2 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1058-422C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412359 | ||||||
chr11:61412390
|
C | T | 2 | a0001c0002t0006g0077a0001c0002t0006g0108 | 2 | HG02083.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1058-453G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412390 | ||||||
chr11:61412506
|
G | C | 1 | a0001c0002t0001g0070 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1058-569C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412506 | ||||||
chr11:61412604
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1058-667T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412604 | ||||||
chr11:61412705
|
G | A | 1 | a0001c0002t0001g0084 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1058-768C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412705 | ||||||
chr11:61412779
|
G | A | 1 | a0001c0002t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1058-842C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412779 | ||||||
chr11:61412887
|
T | C | 1 | a0001c0001t0003g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1058-950A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412887 | ||||||
chr11:61412911
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1058-974A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61412911 | ||||||
chr11:61413007
|
A | T | 43 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 53 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(50): Show |
intron_variant | MODIFIER | c.1058-1070T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413007 | ||||||
chr11:61413317
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1058-1380T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413317 | ||||||
chr11:61413440
|
G | A | 1 | a0001c0002t0001g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1058-1503C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413440 | ||||||
chr11:61413505
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1058-1568G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413505 | ||||||
chr11:61413633
|
C | CA | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0125others(5): Show | 10 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1058-1697dupT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413633 | ||||||
chr11:61413633
|
CAA | C | 6 | a0001c0001t0003g0006a0001c0001t0003g0115a0001c0001t0003g0116others(3): Show | 8 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1058-1698_1058-169 others(6): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413633 | ||||||
chr11:61413747
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1058-1810G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413747 | ||||||
chr11:61413820
|
A | G | 3 | a0001c0001t0002g0007a0001c0001t0002g0127a0001c0001t0002g0128 | 5 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1057+1846T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61413820 | ||||||
chr11:61414109
|
A | T | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1057+1557T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414109 | ||||||
chr11:61414148
|
A | AT | 111 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0001g0018others(108): Show | 140 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.1057+1517dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414148 | ||||||
chr11:61414148
|
A | ATT | 12 | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0024others(9): Show | 13 | HG01081.hp1 HG01257.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1057+1516_1057+151 others(6): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414148 | ||||||
chr11:61414148
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0013 | 2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1057+1508_1057+151 others(14): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414148 | ||||||
chr11:61414313
|
T | C | 2 | a0001c0001t0002g0134a0001c0001t0002g0138 | 2 | HG02622.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1057+1353A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414313 | ||||||
chr11:61414625
|
A | T | 1 | a0001c0002t0001g0011 | 2 | HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1057+1041T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414625 | ||||||
chr11:61414851
|
C | T | 1 | a0001c0002t0001g0078 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1057+815G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414851 | ||||||
chr11:61414862
|
C | A | 1 | a0001c0002t0001g0063 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1057+804G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61414862 | ||||||
chr11:61415073
|
CA | C | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057+592delT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61415073 | ||||||
chr11:61415161
|
C | A | 1 | a0001c0002t0001g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1057+505G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61415161 | ||||||
chr11:61415199
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1057+467G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61415199 | ||||||
chr11:61415594
|
A | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0024 | 2 | NA18950.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1057+72T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 7/9 | chr11 | 61415594 | ||||||
chr11:61415857
|
T | C | 2 | a0001c0002t0001g0073a0001c0002t0001g0078 | 2 | HG01928.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.939-73A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415857 | ||||||
chr11:61415867
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.939-83T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415867 | ||||||
chr11:61415898
|
A | G | 9 | a0001c0001t0001g0015a0001c0001t0001g0132a0001c0001t0001g0133others(6): Show | 10 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.939-114T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415898 | ||||||
chr11:61415902
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.939-118T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415902 | ||||||
chr11:61415916
|
C | T | 9 | a0001c0002t0001g0055a0001c0002t0001g0064a0001c0002t0001g0076others(6): Show | 9 | HG01123.hp1 HG01261.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.939-132G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61415916 | ||||||
chr11:61416082
|
C | G | 3 | a0001c0002t0001g0062a0001c0002t0001g0063a0001c0002t0001g0150 | 3 | HG01255.hp1 HG01433.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.938+23G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 6/9 | chr11 | 61416082 | ||||||
chr11:61416557
|
T | A | 1 | a0001c0001t0001g0039 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.524-38A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416557 | ||||||
chr11:61416569
|
C | T | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0111others(9): Show | 14 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-50G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416569 | ||||||
chr11:61416639
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0136others(1): Show | 4 | HG02451.hp2 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.524-120C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416639 | ||||||
chr11:61416739
|
GAATGTTT others(9): Show |
G | 12 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0111others(9): Show | 14 | HG01243.hp2 HG01261.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.524-236_524-221del others(16): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416739 | ||||||
chr11:61416755
|
T | G | 31 | a0001c0001t0001g0015a0001c0001t0001g0117a0001c0001t0001g0132others(28): Show | 39 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(36): Show |
intron_variant | MODIFIER | c.524-236A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61416755 | ||||||
chr11:61417116
|
A | G | 1 | a0001c0002t0001g0011 | 2 | HG01978.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.524-597T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417116 | ||||||
chr11:61417178
|
T | C | 5 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.524-659A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417178 | ||||||
chr11:61417315
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.524-796T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417315 | ||||||
chr11:61417401
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.524-882C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417401 | ||||||
chr11:61417529
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.524-1010C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417529 | ||||||
chr11:61417685
|
T | C | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 52 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(49): Show |
intron_variant | MODIFIER | c.524-1166A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417685 | ||||||
chr11:61417732
|
G | C | 62 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0010others(59): Show | 81 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.524-1213C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417732 | ||||||
chr11:61417746
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.524-1227C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61417746 | ||||||
chr11:61418055
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.524-1536T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418055 | ||||||
chr11:61418231
|
C | A | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 52 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(49): Show |
intron_variant | MODIFIER | c.524-1712G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418231 | ||||||
chr11:61418249
|
G | C | 1 | a0001c0002t0001g0079 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.523+1700C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418249 | ||||||
chr11:61418366
|
T | C | 3 | a0001c0001t0002g0131a0001c0001t0002g0134a0001c0001t0002g0138 | 3 | HG02622.hp1 HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.523+1583A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418366 | ||||||
chr11:61418563
|
C | T | 1 | a0001c0002t0001g0053 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.523+1386G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418563 | ||||||
chr11:61418724
|
C | CT | 3 | a0001c0001t0002g0007a0001c0001t0002g0127a0001c0001t0002g0128 | 5 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1224dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418724 | ||||||
chr11:61418724
|
CT | C | 7 | a0001c0002t0001g0003a0001c0002t0001g0051a0001c0002t0001g0079others(4): Show | 11 | HG01168.hp2 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.523+1224delA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418724 | ||||||
chr11:61418764
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.523+1185C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418764 | ||||||
chr11:61418782
|
A | C | 1 | a0001c0002t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.523+1167T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61418782 | ||||||
chr11:61419143
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.523+806G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419143 | ||||||
chr11:61419197
|
T | A | 1 | a0001c0001t0001g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.523+752A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419197 | ||||||
chr11:61419349
|
A | C | 43 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(40): Show | 53 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(50): Show |
intron_variant | MODIFIER | c.523+600T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419349 | ||||||
chr11:61419510
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.523+439A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419510 | ||||||
chr11:61419896
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.523+53G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419896 | ||||||
chr11:61419897
|
C | G | 5 | a0001c0001t0003g0006a0001c0001t0003g0116a0001c0001t0003g0118others(2): Show | 7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.523+52G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419897 | ||||||
chr11:61419899
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.523+50A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 5/9 | chr11 | 61419899 | ||||||
chr11:61420710
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.274-137G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 3/9 | chr11 | 61420710 | ||||||
chr11:61420795
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-222T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 3/9 | chr11 | 61420795 | ||||||
chr11:61420962
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.274-389G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 3/9 | chr11 | 61420962 | ||||||
chr11:61421642
|
C | G | 1 | a0001c0001t0002g0127 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.55-34G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421642 | ||||||
chr11:61421665
|
T | C | 21 | a0001c0001t0001g0117a0001c0001t0002g0005a0001c0001t0002g0007others(18): Show | 28 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.55-57A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421665 | ||||||
chr11:61421683
|
G | C | 1 | a0001c0002t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.55-75C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421683 | ||||||
chr11:61421712
|
T | G | 13 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0122others(10): Show | 18 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.55-104A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421712 | ||||||
chr11:61421816
|
CTGTTAAT others(21): Show |
C | 1 | a0001c0001t0001g0008 | 2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.55-236_55-209delAA others(26): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421816 | ||||||
chr11:61421834
|
G | C | 30 | a0001c0001t0001g0015a0001c0001t0001g0117a0001c0001t0001g0132others(27): Show | 38 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.55-226C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421834 | ||||||
chr11:61421846
|
A | T | 1 | a0001c0001t0001g0008 | 2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.55-238T>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421846 | ||||||
chr11:61421977
|
C | T | 6 | a0001c0002t0001g0055a0001c0002t0001g0095a0001c0002t0001g0096others(3): Show | 6 | HG01123.hp1 HG01261.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.55-369G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61421977 | ||||||
chr11:61422042
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.55-434T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422042 | ||||||
chr11:61422139
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.55-531A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422139 | ||||||
chr11:61422198
|
G | A | 1 | a0001c0002t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.55-590C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422198 | ||||||
chr11:61422278
|
T | C | 1 | a0001c0002t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.55-670A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422278 | ||||||
chr11:61422471
|
T | C | 3 | a0001c0002t0001g0083a0001c0002t0001g0084a0001c0002t0001g0103 | 3 | NA18988.hp1 NA19075.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.55-863A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422471 | ||||||
chr11:61422507
|
G | A | 1 | a0001c0002t0001g0075 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.55-899C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422507 | ||||||
chr11:61422870
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.55-1262G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422870 | ||||||
chr11:61422903
|
T | C | 142 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0014others(139): Show | 176 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(173): Show |
intron_variant | MODIFIER | c.55-1295A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422903 | ||||||
chr11:61422987
|
G | A | 5 | a0001c0001t0003g0006a0001c0001t0003g0116a0001c0001t0003g0118others(2): Show | 7 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.55-1379C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61422987 | ||||||
chr11:61423026
|
G | A | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(4): Show | 7 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.55-1418C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423026 | ||||||
chr11:61423105
|
C | CA | 70 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0024others(67): Show | 87 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.55-1498dupT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423105 | ||||||
chr11:61423105
|
C | CAA | 33 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0149others(30): Show | 47 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.55-1499_55-1498dup others(2): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423105 | ||||||
chr11:61423105
|
C | CAAA | 10 | a0001c0001t0002g0139a0001c0001t0002g0140a0001c0002t0001g0080others(7): Show | 10 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.55-1500_55-1498dup others(3): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423105 | ||||||
chr11:61423105
|
CA | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0132a0001c0001t0001g0133others(4): Show | 8 | HG02451.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.55-1498delT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423105 | ||||||
chr11:61423132
|
G | T | 113 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(110): Show | 146 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(143): Show |
intron_variant | MODIFIER | c.55-1524C>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423132 | ||||||
chr11:61423169
|
CT | C | 84 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(81): Show | 108 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.55-1562delA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423169 | ||||||
chr11:61423169
|
CTTT | C | 42 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(39): Show | 52 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(49): Show |
intron_variant | MODIFIER | c.55-1564_55-1562del others(3): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423169 | ||||||
chr11:61423325
|
A | C | 1 | a0001c0002t0001g0104 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.55-1717T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423325 | ||||||
chr11:61423417
|
C | T | 13 | a0001c0001t0002g0005a0001c0001t0002g0007a0001c0001t0002g0122others(10): Show | 18 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.55-1809G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423417 | ||||||
chr11:61423568
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.55-1960C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423568 | ||||||
chr11:61423692
|
G | GT | 4 | a0001c0001t0001g0015a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 5 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-2085dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423692 | ||||||
chr11:61423746
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0136 | 3 | HG02451.hp2 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.55-2138A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423746 | ||||||
chr11:61423861
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.55-2253A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423861 | ||||||
chr11:61423875
|
A | C | 1 | a0001c0002t0001g0060 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.55-2267T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61423875 | ||||||
chr11:61424037
|
T | A | 1 | a0001c0001t0001g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.55-2429A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424037 | ||||||
chr11:61424241
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.55-2633C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424241 | ||||||
chr11:61424285
|
T | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.55-2677A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424285 | ||||||
chr11:61424320
|
T | C | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-2712A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424320 | ||||||
chr11:61424514
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.55-2906C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424514 | ||||||
chr11:61424755
|
C | CT | 14 | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 15 | HG01081.hp1 HG01978.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-3148dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424755 | ||||||
chr11:61424882
|
G | C | 21 | a0001c0001t0001g0117a0001c0001t0002g0005a0001c0001t0002g0007others(18): Show | 28 | HG01109.hp1 HG01496.hp1 HG02257.hp2 others(25): Show |
intron_variant | MODIFIER | c.55-3274C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424882 | ||||||
chr11:61424965
|
G | C | 6 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG01261.hp2 HG02895.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-3357C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61424965 | ||||||
chr11:61425144
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.55-3536C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425144 | ||||||
chr11:61425326
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.55-3718C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425326 | ||||||
chr11:61425361
|
A | AT | 2 | a0001c0002t0001g0107a0001c0002t0006g0108 | 2 | NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.55-3754dupA | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425361 | ||||||
chr11:61425423
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+3759G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425423 | ||||||
chr11:61425586
|
G | T | 1 | a0001c0002t0001g0059 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.54+3596C>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425586 | ||||||
chr11:61425662
|
A | G | 1 | a0001c0002t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.54+3520T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425662 | ||||||
chr11:61425783
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.54+3399A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61425783 | ||||||
chr11:61426060
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0132a0001c0001t0001g0133others(6): Show | 10 | HG02451.hp2 HG02572.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.54+3122G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426060 | ||||||
chr11:61426411
|
G | A | 2 | a0001c0002t0001g0085a0001c0002t0001g0086 | 2 | NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.54+2771C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426411 | ||||||
chr11:61426580
|
A | C | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.54+2602T>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426580 | ||||||
chr11:61426820
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.54+2362C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426820 | ||||||
chr11:61426896
|
C | T | 1 | a0001c0002t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.54+2286G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426896 | ||||||
chr11:61426936
|
G | A | 6 | a0001c0001t0001g0117a0001c0001t0003g0006a0001c0001t0003g0114others(3): Show | 8 | HG02630.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+2246C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61426936 | ||||||
chr11:61427026
|
C | CA | 12 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0037others(9): Show | 13 | HG01081.hp1 HG01978.hp1 HG02015.hp1 others(10): Show |
intron_variant | MODIFIER | c.54+2155dupT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | ||||||
chr11:61427026
|
C | CAA | 8 | a0001c0001t0001g0014a0001c0001t0001g0042a0001c0001t0001g0125others(5): Show | 11 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+2154_54+2155dup others(2): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | ||||||
chr11:61427026
|
C | CAAA | 6 | a0001c0001t0001g0015a0001c0001t0001g0129a0001c0001t0001g0130others(3): Show | 7 | HG02572.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+2153_54+2155dup others(3): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | ||||||
chr11:61427026
|
C | CAAAA | 6 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0142others(3): Show | 6 | HG01109.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+2152_54+2155dup others(4): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | ||||||
chr11:61427026
|
C | CAAAAA | 6 | a0001c0001t0001g0136a0001c0001t0002g0005a0001c0001t0002g0137others(3): Show | 9 | HG01496.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+2151_54+2155dup others(5): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | ||||||
chr11:61427026
|
CAAAAA | C | 6 | a0001c0001t0001g0117a0001c0001t0003g0006a0001c0001t0003g0114others(3): Show | 8 | HG02630.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.54+2151_54+2155del others(5): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | ||||||
chr11:61427026
|
CAAAAAAA others(2): Show |
C | 5 | a0001c0001t0001g0013a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 6 | HG01243.hp2 HG01261.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+2147_54+2155del others(9): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427026 | ||||||
chr11:61427052
|
A | AAG | 14 | a0001c0002t0001g0012a0001c0002t0001g0057a0001c0002t0001g0087others(11): Show | 15 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.54+2129_54+2130ins others(2): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427052 | ||||||
chr11:61427052
|
A | AG | 54 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(51): Show | 76 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.54+2129dupC | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427052 | ||||||
chr11:61427052
|
A | G | 1 | a0001c0002t0001g0103 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.54+2130T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427052 | ||||||
chr11:61427074
|
T | C | 70 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(67): Show | 93 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.54+2108A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427074 | ||||||
chr11:61427138
|
C | A | 6 | a0001c0002t0001g0055a0001c0002t0001g0095a0001c0002t0001g0096others(3): Show | 6 | HG01123.hp1 HG01261.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.54+2044G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427138 | ||||||
chr11:61427140
|
T | C | 1 | a0001c0002t0008g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.54+2042A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427140 | ||||||
chr11:61427274
|
G | A | 1 | a0001c0002t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.54+1908C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427274 | ||||||
chr11:61427348
|
G | C | 5 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0004g0045others(2): Show | 5 | HG02451.hp1 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1834C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427348 | ||||||
chr11:61427458
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0111 | 2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.54+1724T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427458 | ||||||
chr11:61427464
|
C | T | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.54+1718G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427464 | ||||||
chr11:61427519
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.54+1663C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427519 | ||||||
chr11:61427567
|
C | A | 1 | a0001c0001t0001g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.54+1615G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427567 | ||||||
chr11:61427607
|
C | G | 2 | a0001c0002t0001g0056a0001c0002t0001g0057 | 2 | HG00099.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.54+1575G>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427607 | ||||||
chr11:61427655
|
G | GA | 5 | a0001c0001t0003g0141a0001c0002t0001g0103a0001c0002t0001g0104others(2): Show | 5 | HG01081.hp2 HG03098.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+1526dupT | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427655 | ||||||
chr11:61427764
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.54+1418T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427764 | ||||||
chr11:61427978
|
A | G | 1 | a0001c0002t0001g0055 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.54+1204T>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61427978 | ||||||
chr11:61428009
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.54+1173A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428009 | ||||||
chr11:61428093
|
C | A | 2 | a0001c0002t0001g0107a0001c0002t0006g0108 | 2 | NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.54+1089G>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428093 | ||||||
chr11:61428094
|
G | A | 1 | a0001c0002t0001g0109 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.54+1088C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428094 | ||||||
chr11:61428118
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.54+1064A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428118 | ||||||
chr11:61428160
|
G | T | 2 | a0001c0002t0001g0053a0001c0002t0001g0054 | 2 | HG02083.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.54+1022C>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428160 | ||||||
chr11:61428501
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.54+681A>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428501 | ||||||
chr11:61428571
|
T | A | 1 | a0001c0002t0001g0110 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.54+611A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428571 | ||||||
chr11:61428817
|
G | A | 70 | a0001c0002t0001g0001a0001c0002t0001g0002a0001c0002t0001g0003others(67): Show | 93 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.54+365C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428817 | ||||||
chr11:61428822
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.54+360G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61428822 | ||||||
chr11:61429116
|
C | T | 1 | a0001c0002t0001g0050 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.54+66G>A | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61429116 | ||||||
chr11:61429131
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.54+51A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 2/9 | chr11 | 61429131 | ||||||
chr11:61429310
|
G | A | 5 | a0001c0001t0001g0015a0001c0001t0001g0144a0001c0001t0001g0145others(2): Show | 6 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-55-20C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429310 | ||||||
chr11:61429441
|
G | A | 45 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(42): Show | 55 | HG01109.hp1 HG01243.hp2 HG01261.hp2 others(52): Show |
intron_variant | MODIFIER | c.-55-151C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429441 | ||||||
chr11:61429505
|
AGCGCCGC others(4): Show |
A | 1 | a0001c0002t0001g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-55-226_-55-216del others(11): Show |
CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429505 | ||||||
chr11:61429516
|
T | G | 115 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(112): Show | 148 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(145): Show |
intron_variant | MODIFIER | c.-55-226A>C | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429516 | ||||||
chr11:61429525
|
G | C | 1 | a0001c0001t0001g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-55-235C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429525 | ||||||
chr11:61429682
|
T | A | 1 | a0001c0002t0001g0150 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-56+232A>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429682 | ||||||
chr11:61429795
|
G | C | 1 | a0001c0001t0001g0151 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-56+119C>G | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429795 | ||||||
chr11:61429856
|
G | A | 1 | a0001c0002t0001g0152 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-56+58C>T | CPSF7 | ENSG00000149532.16 | transcript | ENST00000439958.8 | protein_coding | 1/9 | chr11 | 61429856 |